key: cord-0016266-567xg9an authors: Esteves, Sandro C.; Zini, Armand; Coward, Robert Matthew; Evenson, Donald P.; Gosálvez, Jaime; Lewis, Sheena E. M.; Sharma, Rakesh; Humaidan, Peter title: Sperm DNA fragmentation testing: Summary evidence and clinical practice recommendations date: 2020-10-27 journal: Andrologia DOI: 10.1111/and.13874 sha: b0c1e27f2ff69b0a33c2bf1b900b54ab6e8bc2f4 doc_id: 16266 cord_uid: 567xg9an We herein summarise the evidence concerning the impact of sperm DNA fragmentation in various clinical infertility scenarios and the advances on sperm DNA fragmentation tests. The collected evidence was used to formulate 41 recommendations. Of these, 13 recommendations concern technical aspects of sperm DNA fragmentation testing, including pre‐analytical information, clinical thresholds and interpretation of results. The remaining 28 recommendations relate to indications for sperm DNA fragmentation testing and clinical management. Clinical scenarios like varicocele, unexplained infertility, idiopathic infertility, recurrent pregnancy loss, intrauterine insemination, in vitro fertilisation/intracytoplasmic sperm injection, fertility counselling for men with infertility risk factors and sperm cryopreservation have been contemplated. The bulk evidence supporting the recommendations has increased in recent years, but it is still of moderate to low quality. This guideline provides clinicians with advice on best practices in sperm DNA fragmentation testing. Also, recommendations are provided on possible management strategies to overcome infertility related to sperm DNA fragmentation, based on the best available evidence. Lastly, we identified gaps in knowledge and opportunities for research and elaborated a list of recommendations to stimulate further investigation. Infertility affects over 180 million people worldwide. The male factor is found in nearly 10% of all couples and is responsible for about 50% of infertility cases . Male infertility, in particular, is a disorder of the reproductive system, caused primarily by male factors involving deficiencies in the semen, genetic and congenital conditions, anatomical defects, endocrine disturbances, immunological or functional abnormalities, sexual conditions incompatible with intercourse and chronic illness (Zegers-Hochschild et al., 2017) . The incidence of male infertility has apparently increased in parallel with decay in semen quality (Andersson et al., 2008; Evenson et al., 1999; Swan et al., 2000) . Male factor infertility adversely affects reproductive outcomes even under assisted reproductive technology (ART) settings (Boulet et al., 2015; Nangia et al., 2011) . Despite this fact, the male partner is often neglected during the evaluation and treatment of infertility (Petok, 2015) . A critical aspect relates to the fact that the cause of male infertility remains unexplained in up to 50% of patients using classic assessments, and ART treatments are widely available to successfully bypass the male factor in many cases (Esteves & Chan, 2015; Hamada et al., 2012; Jungwirth et al., 2015) . Male infertility is vast and complex, covering a broad spectrum, including conventional and novel diagnostic methods, hormonal control, genetic and epigenetic regulation, interventional therapy and ART. The development of robust methods for male infertility diagnosis is urgently needed, since the routine semen analysis-the laboratory backbone of infertility investigation-has shown little progress over the years (Barratt et al., 2018) . Sperm DNA integrity is indispensable for the birth of healthy offspring (Krawetz, 2005) . Increasing evidence indicates that sperm DNA fragmentation (SDF), a marker of damaged chromatin, has an independent and remarkable role in male infertility and reproductive success (Agarwal, Majzoub, et al., 2016; Aitken, 2016 Aitken, , 2017a Bui et al., 2018; Esteves, Gosálvez, et al., 2015; Rima et al., 2016; Saleh et al., 2002; Sergerie et al., 2005) . Sperm DNA fragmentation may adversely impact sperm fertilising potential, particularly when DNA damage levels are high (González-Marín et al., 2012; Lopes et al., 1998; Simon et al., 2010 Simon et al., , 2011 . Levels of oxidative stress that are not sufficient to induce cell death via apoptosis can disrupt all sperm function aspects, including motility, sperm-zona recognition, acrosomal exocytosis and sperm-oocyte fusion (Aitken, 2020) . However, spermatozoa with damaged chromatin may retain their fertilising ability (Zenzes et al., 1999) . The mixed results obtained in studies evaluating SDF and fertilisation capacity could be explained, at least in part, by the diverse nature of the DNA damage and the oocyte's repair capacity. Indeed, the impact of SDF on reproductive success will depend on the balance between the extent of DNA damage and the oocyte's DNA repair capacity (Champroux et al., 2016; Menezo et al., 2007) . While the repair process probably occurs at the pronuclei stage before syngamy, it has been postulated that sperm DNA damage exceeding the oocyte's repair capacity-or oocyte's failure to repair DNA damage-influences the embryo development potential and the health of the offspring (Martin et al. 2019; Horta et al., 2020) . In such cases, protaminised sperm chromatin cannot be adequately replaced by histones needed for normal DNA replication . For example, oxidative DNA lesions may lead to transversion mutations (e.g., G-C to T-A), altering gene expression if not repaired by the oocyte base excision repair (BER) enzymes before zygote S-phase. As a result, the embryo may fail to develop or implant in the uterus or may be aborted naturally at a later stage. Conversely, if existing DNA repair mechanisms within the oocyte are able to restore a biologically stable genome, normal syngamy and subsequent embryonic development can occur. Accordingly, it has been suggested that the impact of SDF on reproductive success would be better observed post-fertilisation, and the effect will depend mainly on balance between the type and extent of sperm DNA damage and the oocyte's DNA repair capacity (Champroux et al., 2016; Menezo et al., 2007) . SDF may not be perceived on fertilisation but rather causes a late paternal effect related to paternal gene expression in the 4-to 8-cell embryo (Tesarik et al., 2004) . Horta et al. (2020) recently demonstrated experimentally that despite high levels of induced SDF, IVF fertilisation may occur normally, and SDF can be corrected by oocytes from younger females, thus allowing for normal embryo development. The most convincing evidence of an adverse effect of SDF on fertility comes from animal studies. In these studies, the relationship between SDF and natural or assisted reproduction outcomes is not influenced by confounding variables, as it is in clinical studies (Evenson et al., 1980; Li & Lloyd, 2020) . Human IVF and ICSI models using proven fertile donor oocytes have also been utilised to study the impact of SDF on fertility (Gosálvez et al., 2013; Nuñez-Calonge et al., 2012 ). An ICSI study using donor oocytes of proven fertility showed that SDF rates of nonpregnant couples (34.9%) were higher than that of pregnant couples (25.3%; p < 0.001; Gosálvez et al., 2013) . Using a ROC curve and Youden index, the authors found that a threshold SDF value of 24.8% (by SCD assessed in the neat semen) yielded a 75% sensitivity and 69% specificity for pregnancy prediction. Additionally, a variety of human studies using different designs and endpoints have explored the relationship between SDF and fertility, including natural pregnancy, unexplained infertility, recurrent pregnancy loss (RPL), intrauterine insemination (IUI), in vitro fertilisation (IVF) and intracytoplasmic sperm injection (ICSI). In such studies, however, confounding factors (e.g. female age, presence of comorbidities) may influence the effect magnitude of SDF on reproductive success. Infertile men frequently have high levels of SDF in neat semen. A 2018 systematic review and meta-analysis, including over four thousand men and 27 studies, revealed that the standardized mean difference in SDF rates between infertile versus fertile men was 1.6% (95% confidence interval [CI]: 1.2-2.1; p < 0.001; Santi et al., 2018) . In this report, infertile men were those with unexplained infertility (15 studies) or abnormal routine semen analysis (12 studies), whereas fertile counterparts were men with proven fertility (14 studies), healthy donors (8 studies), volunteers (2 studies) and men with normal routine semen analysis (4 studies). Accordingly, the SDF threshold level that most optimally discriminated infertile from fertile men was 20% (area under the curve [AUC]: 0.84; p < 0.001; sensitivity: 79%; specificity: 86%). Many conditions, including varicocele, chronic illness, accessory gland infections, advanced paternal age, lifestyle, obesity, occupational and environmental factors, medications, ionising and nonionising radiation and heat exposure, have been associated with elevated SDF levels (Esteves, 2019; . These conditions can promote SDF mainly by causing defective spermatogenesis, evoking abortive apoptosis or increasing the generation of reactive oxygen species (ROS). Excessive ROS represent a significant causative factor of SDF in live spermatozoa . Our current understanding of the relationship between SDF and male infertility primarily relates to the comparisons among populations of fertile men (whose fertility may have changed since they last produced an offspring) and infertile men. While time to pregnancy (TTP) of less than 12 months from stopping contraception and ability to conceive should be ideally used as the criterion to classify fertile men (Buck Louis et al., 2014) , this definition is not uniformly applied in all studies (Santi et al., 2018) . Moreover, male infertility has many causes and, therefore, the studied population should be adequately characterised to assess the conditions possibly associated with excessive oxidative stress. Sperm DNA fragmentation testing has been used to attain more indepth knowledge about sperm quality due to the critical function of sperm DNA integrity for healthy embryonic development and successful reproductive outcome. The rationale in performing SDF testing relates primarily to the adverse impact of defective sperm chromatin on reproductive success as a whole rather than sperm fertilising capacity in particular. Nonetheless, the predictive value of SDF as a single contributor to reproductive success is challenging because pregnancy is affected by a multitude of controlled and uncontrolled factors. Moreover, in routine clinical settings, male infertility is often a nonsingle factor condition, which may result from a series of nonexclusive and possibly inter-related events including defective spermatogenesis during chromatin remodelling, oxidative stress, subclinical infections, presence of chromosomal abnormalities, constitutive genetic conditions, genomic modifications, such as telomere-shortening and lifestyle/ environmental stressors. Thus, although SDF predictive values should be considered when interpreting test results, infertility is a couple's problem, and a single test of gamete dysfunction from just one partner is limited to predict treatment outcome. Nonetheless, the existing evidence indicates that the probability of a successful pregnancy outcome (natural and assisted) is influenced by the SDF level. Moreover, a growing body of evidence referenced in this manuscript supports the hypothesis that SDF is associated with various pre-conception developmental impairments and also post-conception issues such as miscarriages and increased susceptibility to progeny diseases. Despite the robust association between SDF and infertility, the limited knowledge of SDF tests' characteristics and a common opinion that SDF is untreatable have prevented the broad application of testing in routine practice . Moreover, clear indications for SDF testing are limited; only recently, clinical practice recommendations on its use were proposed (Agarwal, Majzoub, et al., 2016; Salonia et al., 2020) . The continuous expansion in medical information and the need to refine efficiency in diagnosing and treating clinical conditions have been the driving forces for the clinical practice guidelines (CPG's) role and utility. Currently, about eight guidelines on male infertility have been developed by expert panels from many societies (reviewed by Esteves & Chan, 2015; Roque & Esteves, 2016; Shridharani et al., 2016) . A common trait among all guidelines is the scanty available evidence to elaborate recommendations. Most recommendations are graded 'B', 'C' or 'D', thus indicating that the evidence used to formulate recommendations originates overwhelmingly from nonrandomised studies and expert opinion. With regard to SDF testing, societies like the American Urological Association (AUA) and the American Society for Reproductive Medicine (ASRM) have not recommended the use of SDF testing during the routine infertility evaluation mainly due to insufficient data and lack of effective treatment options to overcome infertility in such cases (Jarow et al., 2011 ; Practice Committee of the American Society for Reproductive Medicine, 2013 Medicine, , 2015 . However, more recently, in 2015, the ASRM guidelines conceded that varicocele repair and antioxidant use might be of value to reduce SDF and that testing for SDF might be clinically informative for IUI, IVF and ICSI outcomes. It also acknowledged that spermatozoa retrieved from the testis of men with elevated SDF in the neat semen could have better DNA quality that ejaculated counterparts (Practice Committee of the American Society for Reproductive Medicine, 2015) . Recently, three CPG included specific recommendations concerning SDF testing Bender Atik et al. 2018; Salonia et al., 2020) . Briefly, the 2017 Society for Translational Medicine guideline included indications for testing . This guideline recommends testing for couples with (a) unexplained infertility, (b) recurrent pregnancy loss (RPL), (c) male patients with risk factors (e.g. inadequate lifestyle, exposure to toxicants), and (d) after failed unexplained IUI, IVF or ICSI. This CPG was the first of its kind to aggregate the available evidence and provide clinicians with guidance for management. Several experts critically analysed the document from many angles (see Esteves, Agarwal, Cho, et al., 2017; Translational Andrology and Urology (Sperm DNA Fragmentation) . The consensus was that the recommendations made were primarily based on low-quality evidence, indicating that more research should be conducted. Reproduction and Embryology (ESHRE) is a vast document that contains a subsection specifically addressing SDF testing . It underscores that SDF testing in couples with RPL could be considered for explanatory purposes. The ESHRE guidelines concluded that there is evidence supporting an association between RPL and SDF, and this association seems to be independent of female factors. However, the guidelines pointed out that the impact of interventions to decrease SDF on RPL warrants further investigation. Lastly, the 2020 European Association of Urology (EAU) guidelines on male infertility dedicated a few sections to SDF testing and the impact of SDF in varicocele and unexplained infertility (Salonia et al., 2020) . The EAU guidelines recommend SDF testing in (a) couples with RPL following natural conception, IUI and IVF/ICSI, and (b) men with unexplained infertility. Moreover, it is suggested that in men with unexplained infertility and elevated SDF, who have experienced failed IUI, IVF, or ICSI, testicular sperm retrieval may be used for ICSI as a way to overcome infertility related to impaired sperm DNA quality. The EAU document underlines that in the latter, patients must balance the risks of undergoing an invasive procedure in an otherwise normozoospermic or unexplained condition. Besides, the EAU guidelines acknowledge the critical role SDF in the pathophysiology of infertility related to varicocele, and the potential benefit of varicocele repair to reduce SDF. A specific recommendation is given in this regard, which underscores that varicocele repair may be considered in men with elevated SDF and otherwise unexplained infertility or who have suffered from failed ART treatment, including RPL and implantation failure. It is implied, therefore, that SDF testing should be used to identify men who could benefit from varicocele repair. Clinical practice guidelines are useful tools to help clinicians to refine the quality of health care provided to men with infertility. CPGs may also deter potentially wrongful or fruitless interventions during the evaluation and management of male infertility (Esteves & Chan, 2015) . Since the publication of the guidelines mentioned above, more data have been made available, and new possible indications for SDF have emerged. Besides, new data unfolded the potential benefit of medical and surgical interventions to decrease SDF. Therefore, we reviewed the existing data on SDF testing indications in a diverse range of clinical scenarios and elaborated recommendations based on the best evidence and expert judgment. The coordinator prepared a summary of findings based on existing systematic reviews and meta-analyses and controlled trials or relevant cohort studies and case reports when the former were not available. The guideline development group (GDG) discussed the summary evidence and provided additional supporting evidence if applicable, which served the basis for the draft recommendations. The coordinator prepared the draft recommendations and discussed them with the GDG to reach an agreement on the final recommendations. For each recommendation, a strength rating based on GDG expert judgment and the grade of recommendation, according to the Oxford Centre for Evidence-Based Medicine Levels of Evidence (OCEBM Levels of Evidence Working Group), was included. The strength rating was based on clinical expertise, taking into account the overall quality of evidence, the balance between risks and benefits, and the likely impact on patient preferences and values. We classified the strength of recommendations as strong or conditional. Strong recommendations imply that most individuals in that situation should receive testing or intervention. By contrast, conditional recommendations imply that various choices might be suitable for individual patients and that healthcare practitioners should help each patient reach a decision coherent with a patient-centred approach. In healthy spermatozoa, the chromatin is characterised by a linear disposition of the nucleotides along each DNA strand and the lack of both single and double DNA strand breaks, nucleotide modifications or base loss (Cortés-Gutiérrez et al., 2014) . The sperm chromatin has plenty of alkali-labile sites, mainly localised in the repetitive DNA sequences, prone to DNA torsion during chromatin packing. Chromatin damage is an inclusive term that accounts for any defects in the DNA structure. These defects include (a) single or double DNA strand breaks, (b) base deletion or modification, (c) interstrand or intrastrand DNA cross-linkage and (d) protamine deficiency and/or mispackage via defective DNA-protein cross-link (reviewed by . It may occur during spermatogenesis, spermiogenesis, epididymal transit or post-ejaculation. In particular, SDF relates to the breaks at the DNA strands, which are termed single-strand (SS-DBs) or double-strand breaks (DS-DBs). SS-DBs give rise to free 5′-3′ ends affecting only one DNA strand, whereas its template remains undamaged. By contrast, DS-DBs are characterised by blunt 5′-3′ ends affecting both DNA strands. As mentioned above, SDF involves multiple causative factors, including varicocele, lifestyle-related habits, exposure to occupational and environmental toxicants, ageing and infections (Agarwal, Majzoub, et al., 2016; Cho et al., 2016; Esteves, Santi, et al., 2020; Evenson et al., 2020) . At the cellular level, these factors can promote DNA breaks through nonmutually exclusive mechanisms, namely, sperm chromatin maturation defects, apoptosis and OS . Transition proteins and protamines replace 85% of histones during spermiogenesis . A highly condensed chromatin arranged in a toroid is formed when cysteine residues of protamines undergo intra-and intermolecular disulfide cross-linking Ward & Coffey, 1991) . This intricate packaging safeguards the sperm chromatin during transport through the male and female reproductive tracts and secures the transfer of intact paternal genome to the oocyte (Gawecka et al., 2015) . In mammalian species, the quality of DNA packing relates to the number of cysteine residues at the protamine level; the higher the number of disulfide bonds, the higher the DNA stability . The DNA molecule would be subjected to a forced twisting if controlled DNA nicking-facilitated by topoisomerase IIhad not taken place . Any process affecting protamination can disrupt chromatin condensation . Faulty chromatin compaction creates an abnormal tertiary chromatin structure that likely prevents the zygote from accessing the proper sequences of the paternal genome for the correct launch of the embryonic developmental programme (Dattilo et al., 2014) . High levels of sperm nuclear chromatin condensation abnormalities have been related to decreased fertilisation rates, decreased embryo quality, elevated embryo development arrest and impaired pregnancy rates (Menezo et al., 2017) . The most critical effect seems to be a block at the 2PN stage or even an absence of sperm nucleus' decondensation (Junca et al., 2012) . Failure to repair the DNA nicks-during histone to protamine replacement-can lead to persistent DNA breaks in viable ejaculated spermatozoa and/or trigger apoptosis. Moreover, defective chromatin maturation in the testis makes spermatozoa more susceptible to ROS attack during transit in the male genital tract, leading to sperm DNA breaks (Muratori et al., 2015) . Nonetheless, viable spermatozoa with abnormal chromatin compaction andnonfragmented DNA can be released in the ejaculate McPherson & Longo, 1993) . Apoptotic markers like caspases, Fas, Bcl-X, p53 and annexin V are present in mature spermatozoa, supporting apoptosis in the generation of DNA fragmentation. Double-strand DNA breaks, controlled by specific DNases, degrade the DNA molecule when caspase or annexin V is detected on the sperm surface (Gorczyca et al., 1993; Muratori et al., 2000 Muratori et al., , 2015 Sakkas et al. 2002; Paasch et al., 2004) . Despite this, the association between apoptotic markers and DNA fragmentation is not unequivocal (Moustafa et al. 2004) . Moreover, the apoptotic processes leading to SDF might be different to some degree from the classic apoptotic pathways in somatic cells (Moustafa et al. 2004 ). Oxidative stress resulting from excessive ROS production during sperm transit through the seminiferous tubules and epididymis has been regarded as the leading underlying causative factor for SDF (Ollero et al., 2001; Sakkas & Alvarez, 2010) . Human spermatozoa are susceptible to OS due to the abundant polyunsaturated fatty acid content in plasma membranes. Besides, the sperm cytoplasm has limited cytosolic content of antioxidant factors. Furthermore, spermatozoa possess reduced DNA damage detection and repair mechanisms (Champroux et al., 2016; Dada, 2017) . ROS attack not only sperm membranes but also nuclear and mitochondrial DNA Muratori et al., 2015; Sakkas & Alvarez, 2010) . Based on the oxidative attack amplitude, ROS can also damage the sperm nucleus by modifying bases, creating abasic sites, chromatin protein cross-linking and DNA strand breaks . Excessive ROS generates oxidised base adducts (e.g. 8-oxo-7,8-dihydro2-deoxyguanosine [8OHdG]), which are cleaved out of the DNA by an enzyme named 8-oxoguanine DNA glycosylase 1 (OGG1) DNA, thus creating an unstable abasic site more vulnerable to fragmentation (Aitken, 2016; Feng et al., 2003; Lopes et al., 1998) . Oxygen radicals and physicochemical factors also activate endogenous caspases and endonucleases, thus acting as intrinsic factors causing SDF. It has been shown that spermatozoa from several species, including humans, have an endogenous nuclease that directly participates in apoptosis (Sotolongo et al., 2005) . Moreover, the presence of DNase activity at the seminal plasma can be an additional source of DNA cleavage (Cortés-Gutiérrez et al., 2019; Sotolongo et al., 2003) . Environmental and occupational toxicants (e.g. phthalate exposure, air pollution, high temperature), lifestyle (e.g. obesity; smoking), infection, fever, radiotherapy, chemotherapy and ageing have been related to SDF (Evenson et al., 2000 (Evenson et al., , 2020 Jurewicz & Hanke, 2011; Jurewicz et al., 2009; O'Flaherty et al., 2008; Rubes et al., 2007; Schmid et al., 2007; Wyrobek et al., 2006) . However, extrinsic factors' potential adverse effect is not universal, suggesting that genetic predisposition gives some individuals the ability to metabolise toxic products with increased efficiency (Chengyong et al., 2012; Evenson & Wixon, 2005; Rubes et al., 2007) . Sperm DNA fragmentation tests were initially developed to detect DNA damage in the spermatozoa of nonhuman species (reviewed by Evenson, 2016 Evenson, , 2017 Evenson, , 2018 . A remarkable association between SDF and fecundity was demonstrated in bull/cow, stallion, and boar studies (Ballachey et al., 1987 (Ballachey et al., , 1988 Didion et al., 2009; Evenson et al., 1994; Kenney et al., 1995) . In 1980, Evenson's landmark publication introduced the concept of SDF as related to pregnancy outcomes in humans (Evenson et al., 1980) . The SDF rates (measured by the sperm chromatin structure assay [SCSA]) were twice as higher in patients attending infertility clinics than men of known fertility. This study also included pregnancy outcomes for bulls, showing that the SDF rates were four times higher in animals of known low fertility than those of high fertility. The existing tests can be group in methods that use (a) enzymatic reactions to label the DNA breaks, (b) controlled DNA denaturation combined with protein depletion as intermediates to reveal the DNA breaks and (c) dyes that bind to relaxed GC-rich motifs. The first category comprises tests that utilise a terminal transferase (e.g. Terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labelling; TUNEL; Figures 1 and 2) or specific enzymes such as the Klenow fragment (e.g. in situ nick translation assay; ISNT) to label the free 3-OH ends of the nucleotide at the DNA break. In the latter, a 5′→3′ polymerase activity is combined with a 3′→5′ exonuclease activity for the elimination of precoding nucleotides and proofread- the fluorescent antibiotic chromomycin A3 staining, given its preference to bind relaxed DNA GC-rich motifs, toluidine blue staining, acridine orange test and aniline blue staining (reviewed by . Notably, given that histone-complexed DNA -stained by acridine orange-fluoresces twice as likely as protamine-complexed DNA (Evenson et al., 1986) , this high DNA stainability sperm fraction, which represents spermatozoa with excess nuclear histones and faulty chromatin condensation, can also be detected by the SCSA. Hence, this test also provides information about chromatin compaction (HDS; see Figure S1 ). Thus, the information provided by each assay does not necessarily line up. Abnormal nucleus condensation is primarily associated with protamine deficiency or protamine mispackage via broken DNA-protein ionic links; by contrast, DNA fragmentation primarily relates to oxidative stress (Aitken, 2017a; Menezo et al., 2017; Muratori et al., 2015; . On this basis, we propose a new nomenclature to embrace the tests into two groups, that is, (1) SDF tests, namely TUNEL, ISNT, SCSA, SCD, and Comet, and (2) Sperm chromatin compaction tests, namely, chromomycin A3 staining, acridine orange staining, toluidine blue staining and aniline blue staining. Tests that measure SDF (e.g. TUNEL, SCSA, SCD and Comet) may be preferable to those that measure chromatin compaction due to the role of oxidative stress in male infertility . However, assessment of chromatin compaction has been suggested to be clinically useful to patients with unexplained infertility and RPL if the results of an SDF test are unremarkable (Evenson, 2016; Evenson et al., 2020) . Table 1 summarises the SDF tests′ characteristics, namely, TUNEL, SCSA, SCD and alkaline Comet. These are the most commonly requested tests by practitioners . Each test may have different clinical thresholds due to the different DNA damage sites detected and the particular technical aspects of each assay (Gawecka et al., 2015) . An in-depth analysis of standardisation, cut-off values, reproducibility and limitations of existing tests is beyond this paper; this information can be found elsewhere Ribas-Maynou et al., 2013; Santi et al., 2018) . Briefly, SDF measured in consecutive ejaculates seems to have low biological variability (Evenson et al., 1991; Zini et al., 2001) . In one study evaluating SDF rates (by SCSA) in consecutive ejaculates, the variation was remarkably lower (~9%) than conventional semen parameters (range: 28%-43% in count, motility, and morphology). Moreover, inter-and intra-observer coefficients of variation, computed for SCSA, SCD and TUNEL (using flow cytometry), are reported to be below 10% (Fernández et al., 2005; Giwercman et al., 2003; McEvoy et al., 2014; Sharma et al., 2010; Sharma, Ahmad, et al., 2016) . Interlaboratory agreement is very high (r > 0.9) for SDF measured using the SCSA Evenson, 2018) or the flow cytometry TUNEL assay (Ribeiro F I G U R E 2 TUNEL Assay (Fluorescence Microscopy). Visualisation of sperm DNA damage using terminal deoxynucleotidyl transferase dUTP nick end labelling (TUNEL). Digoxigenin-dUTP is incorporated to DNA breaks using a terminal transferase; anti-digoxigenin-FITC is used to label the sites where digoxigenin-dUTP is present (green colour). TUNEL + represents spermatozoa presenting DNA damage. Slides were counterstained with propidium iodide (red colour). TUNEL-represents spermatozoa free of DNA breaks F I G U R E 3 Sperm chromatin structure assay (SCSA). Test data (SCSA Diagnostics, Brookings, USA). Left panel (top box): raw data from a flow cytometer showing each of 5,000 spermatozoa as a single dot on a scattergram. Y-axis = green fluorescence with 1,024 gradations (channels) of DNA stainability (intact double-stranded DNA). X-axis = red fluorescence with 1,024 gradations of red fluorescence (singlestrand DNA). Axes shown are 1,024/10. Line at Y = 75 marks the upper boundary of DNA staining of normal sperm chromatin; above that line are spermatozoa (dots) with partially uncondensed chromatin allowing more DNA stainability. Bottom left corner shows gating out of seminal debris. Middle panel: Raw data from left panel are converted by SCSAsoft software (or equivalent) to red/red + green fluorescence. This transforms the angled sperm display in the left panel to a vertical pattern that is often critical for accurately delineating the percentage of spermatozoa with fragmented DNA. Y-axis = total DNA stainability versus. X-axis = red/red + green fluorescence (DFI). Right panel: Frequency histogram of data from middle panel showing computer gating into %DFI and Mean DFI. Bottom box: SCSAsoft software calculations of mean of two independent measures of mean and standard deviation (std dev) of median DFI, %DFI and %HDS (high DNA stainability) Gosálvez, González-Martínez, et al., 2011; Hanson et al., 2018) ; therefore, a fixed abstinence period should be used, in particular, to monitor the results of medical or surgical interventions aimed at decreasing SDF (Esteves, Santi, et al., 2020) . Moreover, it is suggested that patients have 1-2 ejaculations during the week before the test. This advice relates to the fact that the epididymis does not empty all spermatozoa with a single ejaculation (Misell et al., 2006) ; thus, if a patient had not had an ejaculation for an extended period, it is likely that some dead and apoptotic spermatozoa would be released with the new ejaculation. The time elapsed between ejaculation and testing is critical as SDF rates can increase as a function of time post-ejaculation in an individual-dependent manner (Gosálvez et al., 2009) . In experiments using semen donors, SDF rates (assessed by the SCD test) increased remarkably during the first post-ejaculation hours in the neat semen, and also in frozen-thawed specimens incubated with culture medium (Tvrdá et al., 2018) . On this basis, it is suggested that analysis is started as quickly as possible after liquefaction (e.g. 30-60 min in neat semen) or immediately after thawing if the test requires freezing for later SDF assessment. In the latter, immediate specimen freezing should be done after liquefaction is achieved. Experiments on rodents and humans have shown that SDF data measured by SCSA, TUNEL, SCD and Comet in extender are similar to those obtained from specimens that were flash-frozen in liquid nitrogen (Evenson et al., 1994; McEvoy et al., 2014; Young et al., 2003) . However, the evidence is not unequivocal, as some studies show that the type of cryomedia, cryopreservation technique and semen quality might influence post-thaw SDF rates (versus baseline values; Kopeika et al., 2015; Lusignan et al., 2018; Raad et al., 2018; reviewed by Paoli et al., 2019) . The clinical utility of assessing SDF in processed semen (e.g. after gradient centrifugation or swim-up) is not supported by current evidence, as results cannot predict the likelihood of pregnancy (Bungum et al., 2008; Niu et al., 2011) . Moreover, gradient centrifugation might increase SDF in some cases, thus adversely impacting ART pregnancy outcomes, potentially (Muratori et al., 2016; Zini et al., 2000) . Although the best assay to quantify SDF and its optimal thresholds are still to be defined, the four major SDF tests mentioned above (SCSA, Comet, SCD, and TUNEL) provide reliable information about sperm DNA integrity in subfertility. However, it is vital to understand how each test reports results. In SCD and conventional TUNEL, the assessments are carried out manually on one to several hundred spermatozoa, under bright-field (SCD) or fluorescence microscopy (SCD; TUNEL; see with low and high DNA fragmentation is also reported to provide additional discriminatory information (see Figure S2 ). (Sharma, Ahmad, et al., 2016) and 16% for SCD . Comet and SCD, obtained in neat semen) are clinically useful for classifying infertile couples into a statistical probability of prolonged time to achieve natural pregnancy, decreased likelihood of pregnancy by IUI, IVF or ICSI and increased risk of miscarriage (Bungum et al., 2008; Evenson, 2013; Gosálvez et al., 2013; Nicopoullos et al., 2019; Oleszczuk et al., 2016; Vandekerckhove et al., 2016) . These clinical thresholds seem to hold for ICSI cycles using donor oocytes (Gosálvez et al., 2013) . In contrast, TUNEL clinical thresholds for IUI, IVF and ICSI have yielded mixed results, with values ranging from 10% to 36% (Benchaib et al., 2007; Borini et al., 2006; Cho et al., 2017a; Duran et al., 2002; Frydman et al., 2008) . However, the TUNEL studies are not homogenous concerning the SDF measurements, as most of them utilised post-thaw SDF values, which are not predictive of IVF/ ICSI outcomes, as previously mentioned. When only studies utilising neat semen are examined, a TUNEL clinical threshold of ~36% seems optimal to determine the reproductive success probability among couples undergoing IVF/ICSI (Frydman et al., 2008; Henkel et al., 2004) . This implies that the remaining spermatozoa in a given specimen, that is, those without detectable DNA fragmentation, are not necessarily free of damage. The 'iceberg effect' hypothesis was initially proposed by Evenson (Evenson et al., 2002) and Alvarez (Alvarez, 2005) and elaborated further by Gosálvez (Gosálvez et al., 2013 Accordingly, the dynamic assessment of SDF by incubating spermatozoa in vitro and assessing SDF at different time points has been proposed as a way to detect the above mentioned sperm population (Tvrdá et al., 2018) . As with conventional semen analysis, SDF tests cannot perfectly discriminate fertile from infertile men or couples that will have a successful ART cycle from those that will not. Both partners can contribute to a couple′s infertility; thus, any test′s usefulness is also dependent on the other partner′s fertility. Before testing, clinicians should understand the characteristics of SDF assays (e.g. The assay relies on the principle that spermatozoa with DNA fragmentation fail to produce the characteristic halo of dispersed DNA loops that are observed in spermatozoa with nonfragmented DNA, following acid denaturation and removal of nuclear proteins. Sperm suspensions are embedded in agarose gel on slides and treated with an acid denaturation solution (HCl) to generate restricted single-strand DNA motifs at the sites of existing single-or double-strand breaks. The denaturation is stopped, and spermatozoa are exposed to a lysing solution based on DTT, sodium dodecyl sulphate, and NaCl to remove the sperm membrane and nuclear proteins. Then, slides are stained with DAPI (4′,6-diamidino-2-phenylindole) or Diff-Quik, and spermatozoa with nondispersed and dispersed chromatin loops are identified by fluorescence or brightfield microscopy examination,respectively, to calculate the percentage of sperm with DNA fragmentation. The halos correspond to relaxed DNA loops attached to the residual nuclear structure as seen in spermatozoa with low or no SDF. By contrast, spermatozoa with very small or no halos correspond to those exhibiting SDF as confirmed by DNA breakage detection-fluorescence in situ hybridisation, a procedure in which the restricted single-stranded DNA motifs generated from DNA breaks can be detected and quantified. the two-tailed Comet assay can be used to assess and differentiate the type of break in the same spermatozoon. The assay firstly applies neutral lysis and electrophoresis to detect double-strand breaks, and then, by turning the slide 90º and applying alkaline lysis and electrophoresis, single-strand breaks are detected. The Comet assay provides three parameters: Given the critical role of sperm DNA integrity for normal fertilisation, healthy embryo development and successful reproductive outcomes, SDF assessment has been used to acquire information about sperm quality at the molecular level . This section summarises the best available evidence concerning the impact of SDF in usual clinical infertility scenarios (Table 3) . Furthermore, we critically appraise the situations in which SDF testing could help identify the origin of the infertility condition and possibly guide therapeutic strategies. Varicocele represents the most frequent correctable cause of male infertility (Cho et al., 2016; Hamada et al., 2013) . The testis responds to varicocele by producing excessive ROS, which can lead to SDF infertile men showed that varicocele repair decreases SDF . Studies evaluating pregnancy as an endpoint are few, but overall, they support the concept that couples who achieve pregnancy after varicocele repair have lower postoperative SDF rates than those who do not (Mohammed et al., 2015; Ni et al., 2014; . In general, there is a concurrent reduction of OS markers and SDF after varicocele repair (Cho et al., 2017b) . After varicocele treatment, SDF retesting may be useful for monitoring the intervention′s outcome and guiding further management. The persistence of abnormal postoperative SDF values is a poor predictor for both natural and assisted conception. In such cases, couples should be counselled accordingly, and IVF-ICSI offered, as discussed in the next sections. In contrast, the reduction of SDF is a good prognostic factor for conception both naturally and by ART ; the decision to pursue expectant management of ART will be based mainly on female factors. On the other hand, the association between subclinical varicocele (i.e. nonpalpable on physical exam but vein dilation and reflux detected by colour doppler ultrasound ) and SDF remains equivocal. Although a controlled study involving 337 men reported a re- Approximately 10%-30% of couples with infertility have no apparent clinical or laboratory alterations-using conventional diagnostic approaches-to explain their condition Hamada et al., 2012; Moghissi and Wallasch 1983 (Griffith & Grimes, 1990) and is no longer recommended for the routine evaluation of the infertile female. Along these lines, a routine semen analysis is also unable to identify sperm defects at the molecular level TA B L E 2 Sperm DNA fragmentation testing: methods, thresholds and interpretation In the male evaluation, given the ubiquity of oxidative stress contributing to male infertility, tests that measure SDF (e.g. TUNEL, SCSA, SCD and Comet) may be preferred over those that assess chromatin compaction because the former are more specific to detect oxidatively induced DNA damage. Animal and human studies indicate that SDF can be assessed in frozen-thawed specimens as results obtained from fresh or flash-frozen specimens by SCSA, TUNEL, SCD and alkaline Comet tend to be similar. However, some studies demonstrate that post-thaw SDF rates might be increased (versus baseline values) depending on the type of cryomedia, cryopreservation technique and semen quality. In SCSA, TUNEL and SCD, the number of spermatozoa with DNA fragmentation-relative to the total number of spermatozoa analysed-indicates the SDF rate (termed DFI in SCSA). The Comet assay quantifies the amount of DNA fragmentation in each cell. In Comet, the average Comet score (ACS) represents the average amount of DNA fragmentation across 100 individual cells analysed. SDF tests cannot perfectly discriminate couples that will have a successful IUI, IVF or ICSI cycle from those that will not. Overall, SDF rates are consistently higher in infertile men than presumed or confirmed fertile controls, irrespective of the assay used for measurement (Santi et al., 2018 Recurrent pregnancy loss is defined as two or more pregnancy A systematic review and meta-analysis of thirteen prospective studies showed that SDF rates were markedly higher in male partners of women with RPL than male partners of fertile control women Tan et al., 2019) . In these studies, fertile controls were women with proven fertility with one or more live birth or ongoing pregnancy. The predictive power of SDF tests is influenced by type (SS-DB or DS-DB), site (intron or exons) and extent of damage in each cell, as well as the number of affected cells and oocyte′s ability to repair SDF after fertilisation. Zini (2020) Thresholds of about 20% evaluated by TUNEL, SCSA, SCD and alkaline Comet, assessed on neat semen, best discriminate fertile from infertile men. Thresholds of 20%-30% evaluated by SCSA, alkaline Comet and SCD, assessed on neat semen, are clinically useful for classifying infertile couples into a statistical probability of longer time to achieve natural pregnancy, decreased chances of pregnancy by IUI, IVF and ICSI, and increased miscarriage risk. Abnormal SDF levels are found in up to 20% of men with unexplained infertility (i.e. infertility despite no identifiable causative factor and normal routine semen parameters). Abnormal SDF levels increases the likelihood of recurrent pregnancy loss (i.e. two or more pregnancy losses) after natural and assisted conception. The adverse effect of SDF on IVF/ICSI outcomes seems to be lower in ICSI studies than conventional IVF studies. To date, the exact mechanism(s) involved in RPL in couples with SDF is not known. However, it has been speculated that DNA fragmentation not repaired by the oocyte may contribute to poor blastocyst development, implantation failure and miscarriage (Tan et al., 2019) . A proposed mechanism involves oxidative stress. In this scenario, genetic/epigenetic changes in the zygote and developing embryo consequent to increased oxidatively induced SDF could cause RPL (Venkatesh et al., 2011) . Specifically, excessive ROS can promote harm by modifying bases, creating abasic sites, chromatin protein cross-linking and DNA strand breaks (both single and double) depending on the oxidative attack . For instance, excessive ROS may lead to the formation of oxidised base adducts (e.g. 8OHdG). The sperm enzyme OGG1 cleaves oxidised base adducts out of the DNA, which creates a relatively unstable abasic site more prone to fragmentation (Aitken, 2017a; Feng et al., 2003; Lopes et al., 1998) . Subsequently, the oocyte BER system will attempt to replace these oxidised bases by nonoxidised bases to correct the alterations after fertilisation and before syngamy. Animal and human studies have shown that the zygote will respond to sperm DNA damage through a nonapoptotic mechanism if DNA damage exceeds the oocyte repair capacity or DNA repair mechanisms do not function properly. This mechanism acts by slowing paternal DNA replication and possibly producing chromosomal rearrangements, ultimately leading to poor embryonic development, implantation failure and miscarriage (Fernández-Gonzalez et al., 2008; Gawecka et al., 2013; Marchetti & Wyrobek, 2005; Menezo et al., 2007) . In couples with unexplained infertility, IUI′s pregnancy rates decrease when SDF values (using the SCD assay) exceed 20% (Vandekerckhove et al., 2016) . The likelihood of pregnancy success by IUI is also reduced (by 7.0-to 8.7-fold) in the general infertile population when inseminations are carried out with samples from men with SDF levels >30% (measured by the SCSA in the neat semen; Bungum et al., 2004 Bungum et al., , 2007 Duran et al., 2002; Rilcheva et al., 2016 Most IVF/ICSI meta-analyses concur that sperm DNA integrity impacts reproductive success. The studies of Li et al., Zini et al. and Zhao et al. showed that elevated SDF was associated with reduced pregnancy rates with conventional IVF but not ICSI (Li et al., 2006; Zhao et al., 2014; Zini, 2011) . By contrast, Osman et al. and Simon et al. showed that elevated SDF adversely impacted both IVF and ICSI reproductive outcomes (Osman et al., 2015; Simon et al., 2017) . The latter represents the most substantial data compilation to date. (Nicopoullos et al., 2019) . The magnitude of effect size concerning the adverse effect of SDF on IVF and ICSI outcomes seems lower in ICSI studies than conventional IVF studies. The reasons are not fully understood, but a few possibilities to explain these observations have been raised by Lewis (Lewis, 2013) . First, up to 30% of women having ICSI have no detectable problems. They may be fertile, and their oocytes can have more capacity to repair DNA damage even if the injected spermatozoon is of poor quality. This argument is supported by Meseguer and co-workers (Meseguer et al., 2011) , who showed that high-quality oocytes from donors may offset the negative impact of sperm DNA damage on pregnancy. Secondly, in ICSI, the gametes are not subjected to prolonged culture; thus, spermatozoa may have less damage at the time of fertilisation than those exposed to incubation in culture media, as in IVF procedures. In contrast to IVF, ICSI spermatozoa are injected into the oocyte within a few hours of ejaculation. This technical difference may protect them from laboratory-induced damage; iatrogenic damage can occur when spermatozoa is maintained in vitro for long periods . Lastly, spermatozoa can be a source of ROS; if used in IVF, the oocyte may be exposed to oxidative assault during incubation. In ICSI, the oocyte is protected from this attack and can use its energies to repair the SDF immediately following fertilisation. Animal studies have shown intraspecies variation concerning sperm DNA resistance to damage under in vitro conditions, with an evident adverse impact of SDF on embryo development and pregnancy outcomes Johnston et al., 2016) . Increased miscarriage rates seem to be a common feature of While the reasons for the reduced pregnancy rates among IVF/ ICSI couples with elevated SDF are not entirely understood, genetic and epigenetic factors related to impaired sperm chromatin could explain suboptimal reproductive outcomes Esteves, Prudencio, et al., 2014; Mitchell et al., 2006; Strassburger et al., 2000) . The DNA oxidative damage may cause mutations or dysregulate methylation processes and genetic pathways critical for embryo development and implantation (Aitken, 2017a; Dada, 2017; Feng et al., 2003) . Along these lines, a proposed mechanism to explain SDFrelated implantation failure after IVF/ICSI relates to deficiencies of the oocyte repair system to properly fix paternal DNA alterations (Champroux et al., 2016; . Both the oocyte repair capacity and the type and/or complexity of SDF vary from one cell to another, thus differentially affecting the em-bryo′s implantation potential. While both SS-DBs and DS-DBs can be repaired at the same DNA strand by direct ligation of 5′-3′ free ends, thereby evading the production of structural chromosomal abnormalities (Obe et al., 2002; van Gent et al., 2001) , DS-DNA breaks are more difficult to repair because there is no complementary strand to use as a template (Bernstein & Rothstein, 2009; Price & D′Andrea, 2013) . Unrepaired DNA motifs may produce chromosomal rearrangements, which can generate high levels of genome instability. As a result, cell death and sudden embryonic loss may occur (Carrano & Heddle, 1973) . When DNA repair is complete, both the copy′s fidelity and the orthodox gene order housed in the chromosome allow the morula and blastocyst stages to be reached. In this case, the paternal genome would be normally regulated and expressed, and a successful pregnancy would ensue; otherwise, if the DNA repair processes were not wholly effective, implantation failure may occur. The latter seems to occur more often in association with DS-DBs (Ribas- The oocyte repair machinery modulates the adverse effect of elevated SDF on embryo development and pregnancy. However, oocytes of advanced age women are less efficient in repairing sperm DNA damage. The persistence of DNA breaks and mutagenic bases might ultimately increase the risk of embryo genetic and epigenetic defects (Aitken, 2017a; Champroux et al., 2016; Dada, 2017; Jin et al., 2015) . Moreover, the SDF type (SS-DBs or DS-DBs) and quantity might also differentially affect embryo development. In studies using the Comet assay, it has been shown that DS-DBs are more significant than SS-DBs concerning embryo kinetics and implantation (Casanovas et al., 2019; . Despite that, the data concerning the impact of SDF on embryo development remain ambiguous. In a 2011 systematic review compiling 3,226 IVF/ICSI cycles, elevated SDF was associated with impaired embryo development in 11 studies, whereas in 17 studies, the relationship was not evident . In oocyte donation programs, elevated SDF was shown to affect blastulation rates adversely, both in studies using the TUNEL assay (Alvarez Sedó et al., 2017) and the SCD test (Kim et al., 2019; Zheng et al., 2018) , albeit not unequivocally (Antonouli et al., 2019) . Furthermore, ICSI studies using time-lapse technology demonstrated that the time to reach critical embryo development stages is negatively impacted by elevated SDF (by the alkaline Comet assay or SCD test; Casanovas et al., 2019; Wdowiak et al., 2015) . Noteworthy, recent studies evaluating blastocyst ploidy indicate that SDF has no apparent adverse impact on embryo euploidy status (assessed by comprehensive 24-chromosome genetic testing; Figueira et al., 2019; Gat et al., 2017) . Lastly, it has been suggested the health of infants could be impacted when natural or assisted inseminations are carried out with specimens with elevated SDF; the mechanisms are not fully understood, but the involvement of OS-mediated altered expression of critical genes for sperm function, fertilisation and embryo development has been hypothesised (Aitken, 2017a; Rima et al., 2016; Vande Loock et al., 2012) . Although the oocyte may tolerate oxidative sperm DNA damage in terms of fertilisation and pronucleus formation (Twigg et al., 1998) , it is in the embryo′s subsequent development that the impact of oxidatively induced SDF seems to manifest more evidently (Burruel et al., 2013) . This may relate to the presence of high levels of unresolved DNA damage leading to the induction of apoptosis or the creation of elevated mutational loads due to aberrant or defective DNA repair. The hypothesis posed by Aitken (Aitken, 2017b) is that an oxidative attack on sperm DNA can lead to the formation of oxidative base adducts such as 8OHdG. In responding to such damage, spermatozoa can only rely on OGG1 enzyme in the base excision repair pathway (Smith et al., 2013) . This glycosylase cleaves the oxidised base out of the DNA duplex to generate a corresponding abasic site that destabilises the ribose-phosphate backbone leading to a β-elimination or a ring-opening reaction of the ribose unit and a consequential strand break. If this limited DNA repair pathway does not complete its task, 8OHdG residues persist in the spermatozoa and because the oocyte is poorly endowed with OGG1, they will be transferred to the zygote entering the S-phase of the first mitotic division following fertilisation (Aitken et al., 2010; Smith et al., 2013) . This phenomenon′s clinical significance is that 8OHdG residues are highly mutagenic, potentially causing an increase in the mutational load carried by the embryo (Aitken, 2017a), particularly, but not exclusively GC-AT transversions (Ohno et al., 2014) . Similarly, oxidative stress in the germline can result in the formation of lipid aldehyde adducts on DNA involving compounds such as 4-hydroxynonenal and 4-hydroxyhexenal, both of which are also powerfully immunogenic (Feng et al., 2003) . They could be responsible for increasing the mutation and epimutation loads carried by the offspring (Tharmalingam et al., 2017) . Additionally, since the spermatozoon′s centromeres are responsible for orchestrating all cell division in the embryo, it is also possible that oxidative damage to this subcellular structure results in an impairment of ordered mitosis. Thus, deletions or sequence errors may be introduced into the developing embryo because of partial oocyte repair, and the health of resulting offspring may be affected (e.g. epigenetic changes, genetic diseases, metabolic diseases, neurological conditions and cancer; reviewed by Aitken, 2017a; Champroux et al., 2016) . The observed increase in mutational load in children of advanced age fathers (Kong et al., 2012) is an example of the above mechanism-in-action, which resonates with the link between advanced paternal age, oxidative sperm DNA damage and a range of pathologies including dominant genetic diseases in the offspring, achondroplasia and neurodevelopmental disorders (e.g. autism, bipolar disease, schizophrenia; Aitken, 2013 Aitken, , 2017a . The most reliable tests for assessing SDF are SCSA, alkaline Comet, SCD and TUNEL. Conditional Grade B Any of the four SDF tests (SCSA, alkaline Comet, SCD and TUNEL) may provide valid information concerning the probability of reproductive success for couples embarking on IUI, IVF and ICSI. A standardised protocol with strict quality control is essential for a reliable SDF testing result. Tests should be validated by the laboratory, with thresholds established based on the evaluation of fertile and infertile populations. A neat semen sample should be used for SDF testing, collected after ejaculatory abstinence of 2-5 days. Grade B Patients should be asked not to have prolonged abstinence periods before the ejaculation that precedes the one used for testing. A fixed ejaculatory abstinence length should be used for SDF testing when monitoring the effects of medical and surgical interventions aimed at decreasing SDF levels. Grade B Fresh or frozen-thawed specimens can be used for testing, but the analysis should start as quickly as possible after liquefaction (e.g. 30-60 min) or thawing. If a frozen specimen is to be used for SDF testing, freezing should be immediately done after liquefaction is achieved. Grade C-D Overall, thresholds of ~20% (SCSA, TUNEL and SCD), and 26% (alkaline Comet), best discriminate fertile from infertile men. Overall, thresholds exceeding 20%-30% (SCSA, alkaline Comet and SCD) indicate a statistical probability of increased time to achieve natural pregnancy, increased miscarriage risk (after both natural and assisted conception), and low odds of reproductive success by IUI, IVF and ICSI. Grade B SDF results-in combination with the current tools for infertility diagnosis-provide useful information concerning the probability of reproductive success. Grade B SDF tests cannot perfectly discriminate fertile from infertile men or couples that will have a successful IUI, IVF or ICSI cycle from those that will not. The usefulness of any test for one partner is also dependent on the fertility of the other partner. Before testing, clinicians should have some understanding of the characteristics of SDF assays (e.g. sensitivity and specificity, positive and negative predictive value). Abbreviations: SDF: sperm DNA fragmentation; ICSI: intracytoplasmic sperm injection; IUI: intrauterine insemination; IVF: in vitro fertilisation; SCSA: sperm chromatin structure assay; SCD: sperm chromatin dispersion; TUNEL: Terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labelling. Grades of recommendations according to quality of evidence: Grade A: consistent level 1 studies; Grade B: consistent level 2 or 3 studies or extrapolations from level 1 studies; Grade C: level 4 studies or extrapolations from level 2 or 3 studies; Grade D: level 5 or troubling inconsistent or inconclusive studies of any level. Level 1 studies: systematic reviews with homogeneity of randomised controlled trials (RCTs) or level 1 diagnostic studies (1a); individual RCT with narrow confidence interval or validating cohort studies with good reference standards (2b). Level 2 studies: systematic reviews with homogeneity of cohort studies or diagnostic studies (2a); individual cohort study or low quality RCT (2b), exploratory cohort study with good reference standards (2b). Level 3: systematic reviews of case-control studies or moderate quality diagnostic studies (3a), individual case-control studies or nonconsecutive diagnostic studies (3b). Level 4: case-series or poor cohort/case-control studies or case-control diagnostic study. Similarly, there seems to be a link between the high levels of oxidative DNA damage observed in male smokers′ spermatozoa and the increased risk of progeny cancer (Lee et al., 2009) . It has been reported that 80% of the novo structural chromosome aberrations in humans are of paternal origin (Tomar et al., 1984) . Notwithstanding these observations, there is limited clinical data concerning the impact of SDF on offspring's health to date. Reassuringly, it appears that children conceived by IVF and ICSI in couples with SDF do not have adverse birth characteristics (Bungum et al., 2012) . In cases where no causative factor is identified, or elevated SDF persists after treatment, ICSI using testicular spermatozoa has been suggested as an effective way to overcome unexplained ICSI failures (Alharbi et al., 2019; Arafa et al., 2018; Bradley et al., 2016; Cheung et al., 2019; Esteves & Roque, 2019; Esteves, Roque, et al., 2017; Esteves, Sanchez-Martin, et al., 2015; Greco et al., 2005; Herrero et al., 2019; Pabuccu et al., 2017; Xie et al., 2020; Zhang et al., 2019) . The reason explaining the higher reproductive success using testicular spermatozoa for ICSI instead of ejaculated in these cases is not entirely understood. However, it may relate to the lower SDF rates in testicular specimens than in ejaculated and epididymal counterparts and the fact that testicular spermatozoa have not been exposed to oxidative-induced damage during transit across the reproductive tract Greco et al., 2005; Hammoud et al., 2017; Mehta et al., 2015; Moskovtsev et al., 2010 Moskovtsev et al., , 2012 Muratori et al., 2015; O′Connell et al., 2002; Steele et al., 1999; Suganuma et al., 2005; Xie et al., 2020) . Male infertility risk factors include lifestyle conditions (e.g. tobacco smoking, obesity, metabolic syndrome), varicocele, genital infections, advanced age and exposure to toxicants (e.g. environmental, licit or illicit drugs [e.g. cannabis consumption], radiation, chemotherapy). A positive association between exposure to air pollutants toxicants (e.g. particulate matter, nitrogen oxides, sulphur oxides, ozone) and SDF has been documented (Lafuente et al., 2016; Radwan et al., 2016; Rubes et al., 2005) . Environmental and occupational exposure (e.g. polycyclic aromatic hydrocarbons, ionising and nonionising radiation, pesticides, endocrine disruptors, lead) can also increase SDF rates (Evenson & Wixon, 2005; Gandhi et al., 2017; Jamal et al., 2016; Jeng et al., 2016; Miranda-Contreras et al., 2015; Sánchez-Peña et al., 2004; Zhou et al., 2016; Zhu & Qiao, 2015) . Additionally, therapeutic exposure to chemotherapy and radiotherapy can promote SS-DBs and DS-DBs in human spermatozoa (Bujan et al., 2014; Smit, van Casteren, et al., 2010; Ståhl et al., 2006) . Among lifestyle factors, tobacco smoking has an adverse influence on sperm chromatin integrity (Aboulmaouahib et al., 2018; Boeri et al., 2019; Cui et al., 2016; Fraga et al., 1996; Gunes et al., 2018; Kumar et al., 2015; Mostafa et al., 2018; Ranganathan et al., 2019; Sharma, Harlev, et al., 2016) . Cannabis consumption can also impair sperm DNA quality (Verhaeghe et al., 2020) . Along these lines, obesity might also affect sperm DNA quality (Morrison & Brannigan, 2015) , albeit the evidence is less compelling . The likely mechanisms in such patients include excessive peripheral conversion of testosterone to oestrogen, causing hypogonadism, increased ROS levels and increased testicular temperature due to excessive suprapubic fat. Sperm DNA fragmentation increases with paternal age, particularly among men aged 40 years and older (Evenson et al., 2020; Rosiak-Gill et al., 2019; Simon et al., 2014) . et al., 2020) . Advanced paternal age might lead to mismatch DNA repair, which seems to be related to deficient sperm quality control during spermatogenesis (Yatsenko & Turek, 2018) . In turn, these effects may translate into increased SDF, single-gene mutations, and abnormalities in sperm chromosomes, ultimately resulting in poorer reproductive outcomes than that achieved in younger counterparts (Bertoncelli Tanaka et al., 2019; García-Ferreyra et al., 2015) . Clinical data concerning the effects of tobacco smoking cessa- Men with varicocele seeking fertility should be informed that varicocele may cause SDF and that repairing a clinical varicocele may alleviate SDF, potentially increasing the likelihood of reproductive success. Grade B-C SDF testing may help identify patients with a profile that would not fit the standard indication of varicocele repair (e.g. clinical varicocele of any grade and normal/ borderline routine semen analysis) but that can benefit from varicocele repair. Grade C SDF testing may be used to monitor treatment outcomes. Conditional Grade C SDF testing in subfertile men with subclinical varicocele is currently not recommended. Strong Grade C Couples with unexplained infertility, idiopathic infertility and RPL should be informed that abnormal SDF levels may adversely impact their chances of achieving a live birth. Grade B SDF testing in couples with unexplained infertility, idiopathic infertility and RPL can be considered for explanatory purposes. Grade B-C An abnormal SDF test result should prompt a complete male evaluation by a reproductive urologist/andrologist to help identify and possibly treat conditions associated with poor sperm DNA quality. ICSI may be considered if no correctable male factor is identified, or if abnormal SDF levels persist after treatment, particularly among couples with a limited reproductive time window. Grade B Infertile couples eligible for IUI treatment should be informed that abnormal SDF levels may adversely impact their chances of achieving a live birth. Grade B SDF testing may be considered before initiating IUI or after IUI failure. Grade B-C An abnormal SDF test result should prompt a complete male evaluation by a reproductive urologist/andrologist to help identify and possibly treat conditions associated with poor sperm DNA quality. Early ICSI may be considered in IUI eligible couples, or after failed IUI, if the male partner has high SDF levels, provided other measures to decrease SDF have been exhausted. Grade C Infertile couples eligible for conventional IVF treatment should be informed that abnormal SDF levels may adversely impact their chances of achieving a live birth. Infertile couples eligible for ICSI treatment should be informed that abnormal SDF levels may adversely impact their chances of achieving a live birth. Grade B SDF testing may be considered before initiating IVF/ICSI or after unexplained failed IVF/ICSI. Grade B-C An abnormal SDF test result should prompt a complete male evaluation by a reproductive urologist/andrologist to help identify and possibly treat conditions associated with poor sperm DNA quality. Grade D ICSI rather than conventional IVF should be used to overcome infertility related to SDF. Strong Grade B Among couples with ICSI failure and elevated SDF, testicular rather than ejaculated spermatozoa may be considered for sperm injection in subsequent treatment cycles. Grade B The use of testicular spermatozoa in preference over ejaculated spermatozoa for ICSI, when both are available, may be particularly relevant for couples with no apparent reasons for a failed ICSI (e.g. no relevant female factors). This advice implies that a reproductive urologist/andrologist has evaluated the male partner and all possible corrective measures taken to improve overall reproductive health and sperm chromatin integrity. Grade D (Continues) men with unexplained infertility showed that a nutritionist-led dietary program associated with exercise over a 3-to 8-month period was able to help reduce SDF values; in this study, the couples achieved full-term deliveries after the intervention (Faure et al., 2014) . The laboratory evidence of defective sperm chromatin can be useful for patients′ counselling concerning overall reproductive health. It may help implement lifestyle modifications in couples who seek fertility counselling and family planning, particularly in those with infertility risk factors. As in the clinical scenarios previously discussed, male evaluation by a reproductive urologist/andrologist is warranted to assess the coexistent causes of elevated SDF that may be treated. SDF testing may also be used to monitor the effectiveness of health improvement programs on sperm DNA quality. Among patients with high SDF in whom no intervention is available to improve DNA quality, the information provided by the test can help decide the best treatment, IUI or IVF/ICSI, when both options are available. As for infertile men of advanced age, SDF testing results would help counselling about the pros and cons of conception using high SDF specimens. OCEBM b recommendation grade based on levels of evidence SDF testing may be considered to provide laboratory evidence of defective sperm chromatin to couples who seek fertility counselling and family planning, particularly when the male partner has an infertility risk factor. Men with infertility risk factors (e.g. tobacco smoking, obesity, metabolic syndrome, exposure to environmental or occupational toxicants, use of licit or illicit drugs with gonadotoxic effects and advanced paternal age) should be informed that these factors may cause SDF and that lifestyle changes may alleviate SDF, potentially increasing the likelihood of reproductive success. An abnormal SDF test result should prompt a complete male evaluation by a reproductive urologist/andrologist to help identify and possibly treat conditions associated with poor sperm DNA quality. An abnormal SDF test result may be used for counselling, reinforcing the importance of lifestyle changes and avoiding exposure to toxins. Early ICSI may be considered for individuals with persistently high SDF levels despite corrective interventions, mainly when the reproductive window is limited. The information provided by SDF testing may guide the choice of assisted conception modality, IUI, IVF or ICSI, in infertile couples with a male partner of advanced age. Grade D SDF testing may be used to monitor the effects of lifestyle interventions. SDF testing can be considered before sperm cryopreservation to provide additional information about semen quality. The information provided by SDF testing may guide the decision to use IUI or IVF/ ICSI for future conception with cryopreserved spermatozoa-in case both options are available-and the choice of the optimal sperm freezing method. Abbreviations: SDF: sperm DNA fragmentation; RPL: recurrent pregnancy loss; ICSI: intracytoplasmic sperm injection; IUI: intrauterine insemination; IVF: in vitro fertilisation. Grades of recommendations according to quality of evidence: Grade A: consistent level 1 studies; Grade B: consistent level 2 or 3 studies or extrapolations from level 1 studies; Grade C: level 4 studies or extrapolations from level 2 or 3 studies; Grade D: level 5 or troubling inconsistent or inconclusive studies of any level. Level 1 studies: systematic reviews with homogeneity of randomised controlled trials (RCTs) or level 1 diagnostic studies (1a); individual RCT with narrow confidence interval or validating cohort studies with good reference standards (2b). Level 2 studies: systematic reviews with homogeneity of cohort studies or diagnostic studies (2a); individual cohort study or low quality RCT (2b), exploratory cohort study with good reference standards (2b). Level 3: systematic reviews of case-control studies or moderate quality diagnostic studies (3a), individual case-control studies or nonconsecutive diagnostic studies (3b). Level 4: case-series or poor cohort/case-control studies or case-control diagnostic study. Sperm DNA fragmentation rates in the semen of men with a diverse range of cancer types can be as high as or even higher than that of infertile men (Marchlewska et al., 2016; Meseguer et al., 2008) . Although the adverse effect of cancer and related therapy on sperm quality is not universal (Ribeiro et al., 2008) , sperm banking is the only reliable option for fertility preservation in reproductive-aged men (Esteves, Lombardo, et al., 2020) . Specimens are typically collected by masturbation, and the semen is cryopreserved using slow or rapid freezing protocols. Such samples are used for IUI or ART after thawing to allow these patients to father biological children. Before cryopreservation, the semen sample is analysed, and the baseline sperm variables (e.g. count, motility, morphology) are used to determine the ideal number of specimens to bank and prognosticate the assisted conception modality required for future conception. Moreover, a frozen aliquot is thawed for sperm cryosurvival assessment, which also helps estimate the total motile sperm number available and advise about the prospects of assisted conception. The cryopreservation process can harm semen quality as it can increase ROS production, leading to excessive OS (Mazzilli et al., 1995 In this section, we provide recommendations concerning the technical aspects, indications and interpretation of SDF testing based on the evidence that has been identified, collated and analysed (see the summary of evidence in Tables 2 and 3 We also expanded the indication of SDF testing to all couples considering IUI or IVF/ICSI provided the minimum requirements for running an SDF test are met (see Table 1 ). The information provided by the test may help identify and guide management in couples that an elevated SDF could cause IUI or IVF/ICSI failure. In these cases, ICSI rather than IUI or conventional IVF should be recommended. This advice implies that a reproductive urologist/andrologist has evaluated the male partner and all possible corrective measures taken to improve overall reproductive health. In some cases, the reduction in SDF rates may help downgrade the assisted reproduction method, or even help achieve natural conception (reviewed by Esteves, Santi, et al., 2020) . Among couples with ICSI failure, our recommendation for testicular spermatozoa rather than ejaculated spermatozoa is overwhelmingly based on observational studies (reviewed by Esteves & Roque, 2019) . Thus, caution should be exercised in this matter as sperm retrieval is not free of complications. Sperm retrieval and intracytoplasmic testicular sperm injections should be advocated in a considered manner preferentially to couples with ICSI failure after exhausting other resources to decrease SDF. When indicated, sperm retrieval should be carried out by a reproductive urologist/andrologist. Lastly, we included new indications for testing, namely, fertility counselling and family planning, particularly among individuals with infertility risk factors and cancer patients who wish to bank spermatozoa for fertility preservation. The information provided by the SDF test may potentially offer guidance to family planners who are attempting natural conception, particularly among those with infertility risk factors and/or limited reproductive time window. The laboratory evidence of defective sperm chromatin should be used to counsel patients about the overall reproductive health and reinforce the importance of lifestyle modifications, including risk reduction. SDF testing can also be used to monitor patient compliance with health improvement interventions. The risks associated with a prolonged attempt to natural conception should be discussed with those individuals who remain with elevated SDF rates after interventions, and early ICSI may be considered. Outstanding medical care delivery involves providing effective and safe care based on the best possible evidence. The foundations of evidence-based medicine rely on the application of evidence that healthcare providers and patients can understand. Also, care provision should be driven by expert advice and patient-shared decision-making through meaningful conversations (Greenhalgh et al., 2014; Trost & Nehra, 2011) . The literature concerning the clinical utility of SDF testing is increasing steadily, and in the future, the present CPG will undoubtedly need to be updated. CPG are evolving documents owing to the continued growth in medical knowledge. Hence, periodic review and update are of utmost importance to provide stakeholders with the most relevant practice guidance. Based on the published data and discussion of the available evidence, we identified various topics for which evidence is inconclusive or inexistent. The GDG recommends that future research focuses on the gaps in knowledge listed below. • Establish which is the most informative SDF test for different clinical scenarios, and when a combination of tests is indicated. • Develop a prognostic model for an individualised assessment of the chances of live birth and time to pregnancy according to SDF values and patient characteristics. • Elucidate the exact mechanisms of oxidatively induced single-strand and double-strand sperm DNA breaks and further study their effects on reproductive outcomes. • Perform epidemiological studies on the prevalence of elevated SDF among couples with unexplained infertility, RPL, males with idiopathic infertility, men with clinical and subclinical varicocele, couples undergoing IUI, IVF and ICSI, family planners with risk factors for infertility, and cancer patients at reproductive age who will bank spermatozoa. • Study the relationship between implantation failure and RPL, and sperm DNA oxidation. • Study the psychological impact of elevated SDF on men seeking fertility. • Clarify the role of varicocele grade on SDF, and the role of varicocele repair to reduce SDF according to grade, the time needed for SDF improvement, and effects on reproductive outcomes. • Study the effect of varicocele repair on reproductive outcomes in infertile men with clinical varicocele, elevated SDF and routine semen parameters within normal ranges. • Study the association of SDF and subclinical varicocele and the effects of varicocele repair on reproductive outcomes. • Study the impact of lifestyle interventions on sperm DNA quality and their impact on reproductive outcomes (preferable in prospective studies with appropriate controls). • Clarify the role of antioxidant therapy for men with SDF. • Compare the cost-effectiveness of early ICSI versus expectant management in couples with unexplained infertility, RPL, family planners with infertility risk factors (preferably in prospective studies). • Compare laboratory techniques to select spermatozoa with low DNA fragmentation for ICSI, in prospective trials involving couples with elevated SDF, controlled for age and other confounders. • Compare the clinical efficacy of testicular spermatozoa for ICSI, in prospective randomised trials involving couples with elevated SDF, controlled for age and other confounders. • Further research is needed on the clinical SDF thresholds to be used with each SDF test on IUI, IVF, and ICSI, using different endpoints (e.g. live birth, miscarriage). • Clarify the role of oocyte quality on SDF repair. • Establish the value of preimplantation genetic testing in couples with elevated SDF undergoing IVF/ICSI. • Study the role of cryoprotectants and cryopreservation techniques to protect spermatozoa from DNA damage. Male infertility is a common medical condition and a public health concern as it is associated with adverse effects on reproduction, overall health, reduced life expectancy and impaired quality of life. A comprehensive evaluation of male infertility can reveal severe and potentially life-threatening underlying medical conditions. The prevention and management of male and female infertility are integral components of comprehensive sexual and reproductive health services needed to attain a sustainable development goal. Our CPG translates the best existing evidence into recommendations to provide the foundation for standardising care while maintaining clinicians′ autonomy. We herein reviewed the data supporting the indications of SDF testing in different infertility scenarios and elaborated recommendations based on best evidence and expert judgment. • Infertility is a couple′s problem; thus, a single test of gamete dysfunction from just one partner is limited to predict the treatment outcome. However, SDF thresholds may reflect the probability of a successful reproductive outcome influenced by the SDF level and modulated primarily by females age. • While SDF testing is not a replacement for the current tools for infertility diagnosis, it may add independent information about sperm quality, and its integration into fertility clinics may provide better counselling, diagnosis and treatment planning. • Sperm DNA fragmentation testing in the clinic can help to: a. Identify patients with potentially correctable underlying factors causing SDF, including the optimal selection of patients for varicocele repair. b. Provide laboratory evidence of defective sperm chromatin to couples seeking fertility counselling and family planning, particularly when the male partner has infertility risk factors, as a way to counsel about fecundity prospects and reinforce the importance of lifestyle changes and avoid exposure to risk factors. c. Better assess the semen quality of subfertile men of advanced paternal age for counselling and guiding clinical management. d. Monitor the effects of interventions (e.g. varicocele repair, lifestyle changes); e. Identify and guide management in couples where elevated SDF might contribute to unexplained/idiopathic infertility. f. Identify and guide management in couples in whom elevated SDF might contribute to recurrent pregnancy loss and could cause IUI or IVF/ICSI failure. g. Better assess the sperm quality of cancer patients who wish to bank sperm for fertility preservation to guide the choice of assisted conception modality optimally. • The male partner of any infertile couple who is found to have elevated SDF should be evaluated by a reproductive urologist/ andrologist to rule out varicocele and other occult male factors. The reduction in SDF rates may help the couple achieve natural conception, downgrade the assisted reproduction method and increase the likelihood of successful reproductive outcomes with IUI, IVF and ICSI. The editors, for the invitation to contribute this article to the Special Andrological Techniques'. SCE coordinated the GDG and had a leading role in collecting the evidence, drafting the manuscript and handling the GDG's comments. All participants contributed to the guideline development, discussed the key questions, synthetised the evidence, drafted recommendations and writing sections of the manuscript. All authors read and approved the submitted version. SCE declares the receipt of unrestricted research grants and lecture fees from Merck outside the submitted work. PH reports receipt of unrestricted research grants from Merck, IBSA, Gedeon Richter, and MSD, and lecture fees from Merck, Gedeon Richter, MSD, and IBSA outside the submitted work. AZ declares shares in YAD-Tech neutraceuticals. DPE is president director of SCSA Diagnostics, a company with a commercial interest in sperm DNA damage. SEML is an employee of Examenlab Ltd., a university spin-out company with a commercial interest in sperm DNA damage. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The authors confirm that the data supporting the findings of this study are available within the article [and/or] The impact of coexisting sperm DNA fragmentation and seminal oxidative stress on the outcome of varicocelectomy in infertile patients: A prospective controlled study Impact of alcohol and cigarette smoking consumption in male fertility potential: Looks at lipid peroxidation, enzymatic antioxidant activities and sperm DNA damage The Society for Translational Medicine: Clinical practice guidelines for sperm DNA fragmentation testing in male infertility Abstinence time and its impact on basic and advanced semen parameters Insight into oxidative stress in varicocele-associated male infertility: Part 1 Clinical utility of sperm DNA fragmentation testing: Practice recommendations based on clinical scenarios A unique view on male infertility around the globe Male Oxidative Stress Infertility (MOSI): Proposed terminology and clinical practice guidelines for management of idiopathic male infertility Age, the environment and our reproductive future: Bonking baby boomers and the future of sex Oxidative stress and the etiology of male infertility DNA damage in human spermatozoa; important contributor to mutagenesis in the offspring Reactive oxygen species as mediators of sperm capacitation and pathological damage. Molecular Reproduction and Development Impact of oxidative stress on male and female germ cells: Implications for fertility Analysis of the relationships between oxidative stress, DNA damage and sperm vitality in a patient population: Development of diagnostic criteria Mystery of idiopathic male infertility: Is oxidative stress an actual risk? HT-COMET: A novel automated approach for high throughput assessment of human sperm chromatin quality Use of testicular sperm in couples with SCSA-defined high sperm DNA fragmentation and failed intracytoplasmic sperm injection using ejaculated sperm The predictive value of sperm chromatin structure assay Effect of sperm DNA fragmentation on embryo development: Clinical and biological aspects Adverse trends in male reproductive health: We may have reached a crucial 'tipping point' The impact of sperm DNA fragmentation on ICSI outcome in cases of donated oocytes ICSI outcome in patients with high DNA fragmentation: Testicular versus ejaculated spermatozoa Heterogeneity of sperm nuclear chromatin structure and its relationship to fertility of bulls The sperm chromatin structure assay: Relationship with alternate tests of sperm quality and heterospermic performance of bulls Man Up': The importance and strategy for placing male reproductive health centre stage in the political and research agenda Sperm deoxyribonucleic acid fragmentation as a prognostic indicator of assisted reproductive technology outcome ESHRE guideline: recurrent pregnancy loss At loose ends: Resecting a double-strand break Paternal age and assisted reproductive technology: Problem solver or trouble maker? Heavy cigarette smoking and alcohol consumption are associated with impaired sperm parameters in primary infertile men Sperm DNA fragmentation: Paternal effect on early post-implantation embryo development in ART Trends in use of and reproductive outcomes associated with intracytoplasmic sperm injection Intervention improves assisted conception intracytoplasmic sperm injection outcomes for patients with high levels of sperm DNA fragmentation: A retrospective analysis Semen quality and time to pregnancy: The Longitudinal Investigation of Fertility and the Environment Study Reactive oxygen species impact on sperm DNA and its role in male infertility Impact of lymphoma treatments on spermatogenesis and sperm deoxyribonucleic acid: A multicenter prospective study from the CECOS network Spermatozoa DNA damage measured by sperm chromatin structure assay (SCSA) and birth characteristics in children conceived by IVF and ICSI The predictive value of sperm chromatin structure assay (SCSA) parameters for the outcome of intrauterine insemination, IVF and ICSI Sperm chromatin structure assay parameters measured after density gradient centrifugation are not predictive for the outcome of ART Oxidative damage to rhesus macaque spermatozoa results in mitotic arrest and transcript abundance changes in early embryos Reassessing the role of subclinical varicocele in infertile men with impaired semen quality: A prospective study Sperm DNA fragmentation in Italian couples with recurrent pregnancy loss The fate of chromosome aberrations Doublestranded sperm DNA damage is a cause of delay in embryo development and can impair implantation rates Mammalian sperm nuclear organization: Resiliencies and vulnerabilities. Basic and Clinical Andrology The association between sperm DNA fragmentation and reproductive outcomes following intrauterine insemination, a meta analysis GSTM1 null genotype contributes to increased risk of male infertility: A meta-analysis Revisiting aneuploidy profile of surgically retrieved spermatozoa by whole exome sequencing molecular karyotype A single cut-off value of sperm DNA fragmentation testing does not fit all Clinical utility of sperm DNA fragmentation testing: Concise practice recommendations Novel insights into the pathophysiology of varicocele and its association with reactive oxygen species and sperm DNA fragmentation Measuring sperm DNA fragmentation and clinical outcomes of medically assisted reproduction: A systematic review and meta-Analysis Do sperm DNA integrity tests predict pregnancy with in vitro fertilization? Characterization of DNA cleavage produced by seminal plasma using leukocytes as a cell target Two-Tailed Comet Assay (2T-Comet): Simultaneous Detection of DNA Single and Double Strand Breaks Interpreting sperm DNA damage in a diverse range of mammalian sperm by means of the two-tailed comet assay Potential effect of smoking on semen quality through DNA damage and the downregulation of Chk1 in sperm Sperm DNA damage diagnostics: When and why Reactive oxygen species-induced alterations in H19-Igf2 methylation patterns, seminal plasma metabolites, and semen quality The importance of the one carbon cycle nutritional support in human male fertility: A preliminary clinical report Removal of DNA-fragmented spermatozoa using flow cytometry and sorting does not improve the outcome of intracytoplasmic sperm injection DNA damage in human spermatozoa is highly correlated with the efficiency of chromatin remodeling and the formation of 8-hydroxy-2′-deoxyguanosine, a marker of oxidative stress Sperm DNA fragmentation index influences assisted reproductive technology outcome: A systematic review and meta-analysis combined with a retrospective cohort study Boar fertility and sperm chromatin structure status Glutathione and hypotaurine in vitro: effects on human sperm motility, DNA integrity and production of reactive oxygen species Sperm DNA quality predicts intrauterine insemination outcome: A prospective cohort study ESHRE guideline: recurrent pregnancy loss Clinical relevance of routine semen analysis and controversies surrounding the 2010 World Health Organization criteria for semen examination Interventions to prevent sperm DNA damage effects on reproduction Are specialized sperm function tests clinically useful in planning assisted reproductive technology? Novel concepts in male infertility Reproductive outcomes, including neonatal data, following sperm injection in men with obstructive and nonobstructive azoospermia: Case series and systematic review A Strengths-Weaknesses-Opportunities-Threats (SWOT) analysis on the clinical utility of sperm DNA fragmentation testing in specific male infertility scenarios The complex nature of the sperm DNA damage process A systematic review of recent clinical practice guidelines and best practice statements for the evaluation of the infertile male Diagnostic accuracy of sperm DNA degradation index (DDSi) as a potential noninvasive biomarker to identify men with varicocele-associated infertility When to pull the trigger in nonazoospermic infertile men undergoing intracytoplasmic sperm injection? SARS-CoV-2 pandemic and repercussions for male infertility patients: A proposal for the individualized provision of andrological services An update on the clinical assessment of the infertile male Comparison of sperm retrieval and reproductive outcome in azoospermic men with testicular failure and obstructive azoospermia treated for infertility Extended indications for sperm retrieval: Summary of current literature. F1000Res, 8, F1000 Faculty Rev-2054 Reproductive outcomes of testicular versus ejaculated sperm for intracytoplasmic sperm injection among men with high levels of DNA fragmentation in semen: Systematic review and meta-analysis Comparison of reproductive outcome in oligozoospermic men with high sperm DNA fragmentation undergoing intracytoplasmic sperm injection with ejaculated and testicular sperm An update on clinical and surgical interventions to reduce sperm DNA fragmentation in infertile men Definitions and relevance of unexplained infertility in reproductive medicine Unexplained infertility A translational medicine appraisal of specialized andrology testing in unexplained male infertility Critical appraisal of World Health Organization′s new reference values for human semen characteristics and effect on diagnosis and treatment of subfertile men Sperm chromatin structure assay (SCSA®) The Sperm Chromatin Structure Assay (SCSA(®) and other sperm DNA fragmentation tests for evaluation of sperm nuclear DNA integrity as related to fertility Evaluation of sperm chromatin structure and DNA strand breaks is an important part of clinical male infertility assessment Sperm Chromatin Structure Assay (SCSA®): Evolution from origin to clinical utility Changes in accessibility of DNA to various fluorochromes during spermatogenesis Relation of mammalian sperm chromatin heterogeneity to fertility Relationships between the age of 25,445 men attending infertility clinics and sperm chromatin structure assay (SCSA®) defined sperm DNA and chromatin integrity Characteristics of human sperm chromatin structure following an episode of influenza and high fever: A case study Utility of the sperm chromatin structure assay as a diagnostic and prognostic tool in the human fertility clinic Comparative sperm chromatin structure assay measurements on epiillumination and orthogonal axes flow cytometers Sperm chromatin structure assay: Its clinical use for detecting sperm DNA fragmentation in male infertility and comparisons with other techniques Flow cytometric evaluation of boar semen by the sperm chromatin structure assay as related to cryopreservation and fertility Environmental toxicants cause sperm DNA fragmentation as detected by the Sperm Chromatin Structure Assay (SCSA®) Data analysis of two in vivo fertility studies using Sperm Chromatin Structure Assay-derived DNA fragmentation index vs. pregnancy outcome In subfertile couple, abdominal fat loss in men is associated with improvement of sperm quality and pregnancy: A case-series Diagnostic accuracy of sperm chromatin dispersion test to evaluate sperm deoxyribonucleic acid damage in men with unexplained infertility Mutational spectrum and genotoxicity of the major lipid peroxidation product, trans-4-hydroxy-2-nonenal, induced DNA adducts in nucleotide excision repair-proficient and -deficient human cells Simple determination of human sperm DNA fragmentation with an improved sperm chromatin dispersion test Long-term effects of mouse intracytoplasmic sperm injection with DNA-fragmented sperm on health and behavior of adult offspring ICSI using surgically retrieved testicular sperm of non-azoospermic men with high sperm DNA fragmentation index and blastocyst ploidy: A safe approach Smoking and low antioxidant levels increase oxidative damage to sperm DNA Adequate ovarian follicular status does not prevent the decrease in pregnancy rates associated with high sperm DNA fragmentation Impaired hypothalamic-pituitary-testicular axis activity, spermatogenesis, and sperm function promote infertility in males with lead poisoning High aneuploidy rates observed in embryos derived from donated oocytes are related to male aging and high percentages of sperm DNA fragmentation Multiple determinations of sperm DNA fragmentation show that varicocelectomy is not indicated for infertile patients with subclinical varicocele Sperm DNA fragmentation index does not correlate with blastocyst aneuploidy or morphological grading Luminal fluid of epididymis and vas deferens contributes to sperm chromatin fragmentation Mouse zygotes respond to severe sperm DNA damage by delaying paternal DNA replication and embryonic development Utility and predictive value of human standard semen parameters and sperm DNA dispersion for fertility potential Types, causes, detection and repair of DNA fragmentation in animal and human sperm cells Presence of DNA strand breaks and increased sensitivity of DNA in situ to denaturation in abnormal human sperm cells: Analogy to apoptosis of somatic cells Can DNA fragmentation of neat or swim-up spermatozoa be used to predict pregnancy following ICSI of fertile oocyte donors? Sperm deoxyribonucleic acid fragmentation dynamics in fertile donors A Comparison of Sperm DNA Damage in the Neat Ejaculate of Sperm Donors and Males Presenting for their Initial Seminogram Shorter abstinence decreases sperm deoxyribonucleic acid fragmentation in ejaculate Unpacking the mysteries of sperm DNA fragmentation: Ten frequently asked questions Relationships between the dynamics of iatrogenic DNA damage and genomic design in mammalian spermatozoa from eleven species. Molecular Reproduction and Development Sperm DNA fragmentation in zebrafish (Danio rerio) and its impact on fertility and embryo viability -Implications for fisheries and aquaculture Efficient treatment of infertility due to sperm DNA damage by ICSI with testicular spermatozoa Evidence based medicine: A movement in crisis? The validity of the postcoital test Role of genetics and epigenetics in male infertility Smoking-induced genetic and epigenetic alterations in infertile men Insight into oxidative stress in varicocele associated male infertility: Part 2 Unexplained male infertility: Diagnosis and management Testicular spermatozoa are of better quality than epididymal spermatozoa in patients with obstructive azoospermia The impact of ejaculatory abstinence on semen analysis parameters: A systematic review Influence of deoxyribonucleic acid damage on fertilization and pregnancy ICSI outcomes using testicular spermatozoa in non-azoospermic couples with recurrent ICSI failure and no previous live births A comparison between two assays for measuring seminal oxidative stress and their relationship with sperm DNA fragmentation and semen parameters Female ageing affects the DNA repair capacity of oocytes in IVF using a controlled model of sperm DNA damage in mice The influence of organophosphate and carbamate on sperm chromatin and reproductive hormones among pesticide sprayers The optimal evaluation of the infertile male: Best practice statement reviewed and validity confirmed Evaluation of sperm DNA fragmentation using multiple methods: A comparison of their predictive power for male infertility Sperm quality and DNA integrity of coke oven workers exposed to polycyclic aromatic hydrocarbons Effect of sperm DNA fragmentation on the clinical outcomes for in vitro fertilization and intracytoplasmic sperm injection in women with different ovarian reserves Reduced sperm DNA longevity is associated with an increased incidence of still born evidence from a multi-ovulating sequential artificial insemination animal model Sperm nucleus decondensation, hyaluronic acid (HA) binding and oocyte activation capacity: Different markers of sperm immaturity? Case reports EAU guidelines of male infertility Exposure to phthalates: Reproductive outcome and children health. A review of epidemiological studies Environmental factors and semen quality Dietary patterns and their relationship with semen quality Relationships between sperm chromatin structure, motility and morphology of ejaculated sperm, and seasonal pregnancy rate Clinical significance of subclinical varicocelectomy in male infertility: Systematic review and meta-analysis Effect of sperm DNA fragmentation on embryo quality in normal responder women in in vitro fertilization and intracytoplasmic sperm injection Rate of de novo mutations and the importance of father′s age to disease risk The effect of cryopreservation on the genome of gametes and embryos: Principles of cryobiology and critical appraisal of the evidence Paternal contribution: New insights and future challenges Outcome of varicocelectomy with different degrees of clinical varicocele in infertile male Tobacco use increases oxidative DNA damage in sperm -Possible etiology of childhood cancer Outdoor air pollution and sperm quality Does sperm DNA fragmentation correlate with semen parameters? Paternal smoking, genetic polymorphisms in CYP1A1 and childhood leukemia risk The place of sperm DNA fragmentation testing in current day fertility management DNA fragmentation index (DFI) as a measure of sperm quality and fertility in mice Vitrification and conventional freezing methods in sperm cryopreservation: A systematic review and meta-analysis Correlation of sperm DNA damage with IVF and ICSI outcomes: A systematic review and meta-analysis Female age affects the utility of sperm DNA fragmentation in predicting IVF and ICSI outcomes Reactive oxygen species: Potential cause for DNA fragmentation in human spermatozoa Effects of different cryopreservation methods on DNA integrity and sperm chromatin quality in men Sperm DNA fragmentation testing: A cross sectional survey on current practices of fertility specialists Understanding sperm DNA fragmentation Insights on the predictive accuracy of the sperm DNA fragmentation tests on male infertility Sperm DNA fragmentation testing in patients with subclinical varicocele: Is there any evidence? Sperm DNA fragmentation and mitochondrial membrane potential combined are better for predicting natural conception than standard sperm parameters Mechanisms and consequences of paternally-transmitted chromosomal abnormalities Sperm DNA fragmentation index and hyaluronan binding ability in men from infertile couples and men with testicular germ cell tumor DNA damage and repair in the female germline: contributions to ART Human sperm cryopreservation and reactive oxygen species (ROS) production Development of a simplified method of human semen storage for the testing of sperm DNA fragmentation using the Halosperm G2 test kit Chromatin structure-function alterations during mammalian spermatogenesis: DNA nicking and repair in elongating spermatids Sperm DNA fragmentation and recurrent pregnancy loss: A systematic review and meta-analysis Higher pregnancy rates using testicular sperm in men with severe oligospermia Evaluation of sperm DNA structure, fragmentation and decondensation: An essential tool in the assessment of male infertility Expression profile of genes coding for DNA repair in human oocytes using pangenomic microarrays, with a special focus on ROS linked decays The effect of cancer on sperm DNA fragmentation as measured by the sperm chromatin dispersion test Effect of sperm DNA fragmentation on pregnancy outcome depends on oocyte quality Effects of occupational exposure to pesticides on semen quality of workers in an agricultural community of Merida state A stable isotope-mass spectrometric method for measuring human spermatogenesis kinetics in vivo Outcome of ICSI with ejaculated spermatozoa in a series of men with distinct ultrastructural flagellar abnormalities Acridine orange and flow cytometry: Which is better to measure the effect of varicocele on sperm DNA integrity? Unexplained infertility Metabolic syndrome and infertility in men A comparison of ejaculated and testicular spermatozoa aneuploidy rates in patients with high sperm DNA damage Testicular spermatozoa have statistically significantly lower DNA damage compared with ejaculated spermatozoa in patients with unsuccessful oral antioxidant treatment Cause-specific treatment in patients with high sperm DNA damage resulted in significant DNA improvement The effect of cigarette smoking on human seminal parameters Relationship between ROS production, apoptosis and DNA denaturation in spermatozoa from patients examined for infertility Functional and ultrastructural features of DNA-fragmented human sperm Investigation on the origin of sperm DNA fragmentation: Role of apoptosis, immaturity and oxidative stress Variation of DNA fragmentation levels during density gradient sperm selection for assisted reproduction techniques: A possible new male predictive parameter of pregnancy? National study of factors influencing assisted reproductive technology outcomes with male factor infertility Sperm protamine mRNA ratio and DNA fragmentation index represent reliable clinical biomarkers for men with varicocele after microsurgical varicocele ligation A comprehensive investigation of sperm DNA damage and oxidative stress injury in infertile patients with subclinical, normozoospermic, and astheno/oligozoospermic clinical varicocoele Novel use of COMET parameters of sperm DNA damage may increase its utility to diagnose male infertility and predict live births following both IVF and ICSI Sperm chromatin structure assay results after swim-up are related only to embryo quality but not to fertilization and pregnancy rates following IVF An improved experimental model for understanding the impact of sperm DNA fragmentation on human pregnancy following ICSI Chromosomal aberrations: Formation, identification and distribution. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis The Oxford Levels of Evidence 2. Oxford Centre for Evidence-Based Medicine Mitochondrial DNA deletions and nuclear DNA fragmentation in testicular and epididymal human sperm Characterization of sperm chromatin quality in testicular cancer and Hodgkin′s lymphoma patients prior to chemotherapy 8-oxoguanine causes spontaneous de novo germline mutations in mice Prevalence of high DNA fragmentation index in male partners of unexplained infertile couples Sperm chromatin structure assay in prediction of in vitro fertilization outcome Characterization of subsets of human spermatozoa at different stages of maturation: Implications in the diagnosis and treatment of male infertility Improved cryopreservation of spermatozoa using vitrification: Comparison of cryoprotectants and a novel device for long-term storage The effect of sperm DNA fragmentation on live birth rate after IVF or ICSI: A systematic review and meta-analysis Cryopreservation and thawing is associated with varying extent of activation of apoptotic machinery in subsets of ejaculated human spermatozoa Testicular versus ejaculated spermatozoa in ICSI cycles of normozoospermic men with high sperm DNA fragmentation and previous ART failures Cryopreservation of sperm: Effects on chromatin and strategies to prevent them Infertility counseling (or the lack thereof) of the forgotten male partner Practice Committee of the American Society for Reproductive Medicine Diagnostic evaluation of the infertile female: a committee opinion Practice Committee of the American Society for Reproductive Medicine Practice Committee of the American Society for Reproductive Medicine Chromatin remodeling at DNA double-strand breaks Cryopreservation media differentially affect sperm motility, morphology and DNA integrity Exposure to ambient air pollution-does it affect semen quality and the level of reproductive hormones? Deterioration of semen quality and sperm-DNA integrity as influenced by cigarette smoking in fertile and infertile human male smokers-A prospective study Single and double strand sperm DNA damage: Different reproductive effects on male fertility Comprehensive analysis of sperm DNA fragmentation by five different assays: TUNEL assay, SCSA, SCD test and alkaline and neutral Comet assay Inter-and intra-laboratory standardization of TUNEL assay for assessment of sperm DNA fragmentation Sperm nuclear apoptotic DNA fragmentation in men with testicular cancer Sperm DNA integrity test and assisted reproductive technology (Art) outcome Oxidative stress induced damage to paternal genome and impact of meditation and yoga -Can it reduce incidence of childhood cancer? The effect of sperm DNA fragmentation on miscarriage rates: A systematic review and meta-analysis Effect of varicocele repair on sperm DNA fragmentation: A systematic review and meta-analysis A systematic review of clinical practice guidelines and best practice statements for the diagnosis and management of varicocele in children and adolescents Effect of varicocele repair on sperm DNA fragmentation: A review Age-related changes in human sperm DNA integrity Episodic air pollution is associated with increased DNA fragmentation in human sperm without other changes in semen quality GSTM1 genotype influences the susceptibility of men to sperm DNA damage associated with exposure to air pollution Sperm chromatin condensation in infertile men with varicocele before and after surgical repair Sperm DNA fragmentation: Mechanisms of origin, impact on reproductive outcome, and analysis Nature of DNA damage in ejaculated human spermatozoa and the possible involvement of apoptosis Negative effects of increased sperm DNA damage in relation to seminal oxidative stress in men with idiopathic and male factor infertility Increased sperm nuclear DNA damage in normozoospermic infertile men: A prospective study 2020 European Association of Urology Sexual and Reproductive Health Guidelines Organophosphorous pesticide exposure alters sperm chromatin structure in Mexican agricultural workers Sperm DNA fragmentation index as a promising predictive tool for male infertility diagnosis and treatment management -Meta-analyses The effects of male age on sperm DNA damage in healthy non-smokers Longitudinal study of sperm DNA fragmentation as measured by terminal uridine nick end-labelling assay A meta-analysis to study the effects of body mass index on sperm DNA fragmentation index in reproductive age men Terminal deoxynucleotidyl transferase dUTP nick end labelling (TUNEL) assay using bench top flow cytometer for evaluation of sperm DNA fragmentation in fertility laboratories: Protocol, reference values, and quality control Cigarette smoking and semen quality: A new meta-analysis examining the effect of the 2010 World Health Organization laboratory methods for the examination of human semen TUNEL as a test for sperm DNA damage in the evaluation of male infertility The significance of clinical practice guidelines on adult varicocele detection and management Clinical significance of sperm DNA damage in assisted reproduction outcome Review: Diagnosis and impact of sperm DNA alterations in assisted reproduction Sperm DNA damage measured by the alkaline Comet assay as an independent predictor of male infertility and in vitro fertilization success Paternal influence of sperm DNA integrity on early embryonic development Sperm DNA damage has a negative association with live-birth rates after IVF Clinical correlates of the biological variation of sperm DNA fragmentation in infertile men attending an andrology outpatient clinic Decreased sperm DNA fragmentation after surgical varicocelectomy is associated with increased pregnancy rate Sperm DNA integrity in cancer patients before and after cytotoxic treatment The presence of a truncated base excision repair pathway in human spermatozoa that is mediated by OGG1 An endogenous nuclease in hamster, mouse, and human spermatozoa cleaves DNA into loop-sized fragments Ability of hamster spermatozoa to digest their own DNA The applicability of the flow cytometric sperm chromatin structure assay in epidemiological studies Sperm DNA integrity in testicular cancer patients A comparison of DNA damage in testicular and proximal epididymal spermatozoa in obstructive azoospermia Very low sperm count affects the result of intracytoplasmic sperm injection Decline in fertility of mouse sperm with abnormal chromatin during epididymal passage as revealed by ICSI The role of sperm DNA fragmentation testing in predicting intra-uterine insemination outcome: A systematic review and meta-analysis The question of declining sperm density revisited: An analysis of 101 studies published 1934-1996 Association between sperm DNA fragmentation and idiopathic recurrent pregnancy loss: A systematic review and meta-analysis Late, but not early, paternal effect on human embryo development is related to sperm DNA fragmentation Low-dose ionizing radiation exposure, oxidative stress and epigenetic programing of health and disease Cryopreservation-induced human sperm DNA damage is predominantly mediated by oxidative stress rather than apoptosis Preferential paternal origin of de novo structural chromosome rearrangements Guideline-based management of male infertility: Why do we need it? Dynamic assessment of human sperm DNA damage I: The effect of seminal plasma-sperm co-incubation after ejaculation Oxidative damage to DNA in human spermatozoa does not preclude pronucleus formation at intracytoplasmic sperm injection A limited number of double-strand DNA breaks is sufficient to delay cell cycle progression Preterm newborns show slower repair of oxidative damage and paternal smoking associated DNA damage Sperm chromatin dispersion test before sperm preparation is predictive of clinical pregnancy in cases of unexplained infertility treated with intrauterine insemination and induction with clomiphene citrate Cytogenetic, Y chromosome microdeletion, sperm chromatin and oxidative stress analysis in male partners of couples experiencing recurrent spontaneous abortions Cannabis consumption might exert deleterious effects on sperm nuclear quality in infertile men DNA packaging and organization in mammalian spermatozoa: Comparison with somatic cells The effect of sperm DNA fragmentation on the dynamics of the embryonic development in intracytoplasmatic sperm injection Significant decrease in sperm deoxyribonucleic acid fragmentation after varicocelectomy Advancing age has differential effects on DNA damage, chromatin integrity, gene mutations, and aneuploidies in sperm Sperm genomic integrity by TUNEL varies throughout the male genital tract Reproductive genetics and the aging male Evaluation of chromosome breakage and DNA integrity in sperm: An investigation of remote semen collection conditions Effect of varicocelectomy and/or mast cells stabilizer on sperm DNA The international glossary on infertility and fertility care Detection of benzo[a]pyrene diol epoxide-DNA adducts in embryos from smoking couples: Evidence for transmission by spermatozoa Testicular spermatozoon is superior to ejaculated spermatozoon for intracytoplasmic sperm injection to achieve pregnancy in infertile males with high sperm DNA damage Whether sperm deoxyribonucleic acid fragmentation has an effect on pregnancy and miscarriage after in vitro fertilization/intracytoplasmic sperm injection: A systematic review and meta-analysis Sperm DNA damage has a negative effect on early embryonic development following in vitro fertilization Sperm quality and DNA damage in men from Jilin Province, China, who are occupationally exposed to ionizing radiation Male reproductive toxicity of bisphenol A Relationship between sperm aneuploidy, sperm DNA integrity, chromatin packaging, traditional semen parameters, and recurrent pregnancy loss Are sperm chromatin and DNA defects relevant in the clinic? Sperm DNA damage is associated with an increased risk of pregnancy loss after IVF and ICSI: Systematic review and meta-analysis Are varicoceles associated with increased deoxyribonucleic acid fragmentation? Is sperm DNA damage associated with IVF embryo quality? A systematic review Biologic variability of sperm DNA denaturation in infertile men Influence of initial semen quality on the integrity of human sperm DNA following semen processing Are tests of sperm DNA damage clinically useful?: Pros and Cons Additional supporting information may be found online in the Supporting Information section. How to cite this article Sperm DNA fragmentation testing: Summary evidence and clinical practice recommendations