key: cord-0967746-ll6mjhz1 authors: Serrano-Lorenzo, Pablo; Coya, Olga N.; López-Jimenez, Ana; Blázquez, Alberto; Delmiro, Aitor; Lucía, Alejandro; Arenas, Joaquín; Martín, Miguel A. title: Plasma LDH: A specific biomarker for lung affectation in COVID-19? date: 2021-04-21 journal: Pract Lab Med DOI: 10.1016/j.plabm.2021.e00226 sha: e9cc6a0c2051fe6ba181556186249b54dab5ab01 doc_id: 967746 cord_uid: ll6mjhz1 OBJECTIVES: We aimed to determine whether the plasma profile of lactate dehydrogenase (LDH) isoenzymes is altered in patients with COVID-19, and whether this is attributable to a specific release of LDH-3, the main LDH isoenzyme expressed in lungs. DESIGN: and Methods: We collected fresh plasma aliquots from 17 patients (LDH range, 281 to 822 U/L) and seven controls (LDH < 230 U/L). In-gel relative activity of the different LDH isoenzymes was determined by electrophoresis and densitometric analysis. RESULTS: Despite the expected higher total LDH activity levels in patients (p<0.001), the in-gel relative activities of LDH isoenzymes did not differ between patients and controls (all p>0.05). We found no correlation between total plasma LDH activity and the in-gel relative activities of the different LDH isoenzymes, including LDH-3. Likewise, there was no correlation between LDH-3 and various routine haematological and serum parameters that have been previously reported to be altered in COVID-19 (such as lymphocyte count, albumin, alanine and aspartate aminotransferase, creatinine, C-reactive protein, or ferritin). CONCLUSIONS: Our findings suggest that elevation of plasma LDH activity in patients with COVID-19 is not associated to a specific release of LDH-3 into the bloodstream, and do not support the use of LDH as a specific biomarker for lung affectation in patients with COVID-19. Identification of laboratory predictors of progression towards severity and fatality is needed for an efficient management of patients with coronavirus disease 2019 (COVID- 19) [1, 2] . In this effect, several biochemical analytes that show abnormal values in severely affected patients have been proposed as disease biomarkers, including among others serum [3] [4] [5] [6] [7] [8] [9] or nasopharyngeal lactate dehydrogenase (LDH) activity [10] . LDH (EC 1.1.1.27) is a hydrogen transfer cytoplasmatic enzyme that catalyses the oxidation of L-lactate to pyruvate with nicotinamide-adenine dinucleotide (NAD) + as hydrogen acceptor, the final reaction in the anaerobic glycolysis pathway [11] . This enzyme is composed of four subunits by the combination of two proteins, M and H, which are expressed mainly in skeletal and heart muscle. Five different isoenzymes, LDH-1 (H4), LDH-2 (H3M), LDH-3 (H2M2), LDH-4 (HM3) and LDH-5 (M4), are detected in plasma by electrophoresis, and since they areat least partlytissuespecific, analysis of the isoenzyme profile could help to identify the main source of LDH release and thus to get insight into the biological significance of this biomarker. Due to specific isoenzyme differences in efficiency for conversion of pyruvate to lactate [12] , the major type of LDH expressed in a particular tissue depends on its metabolic demands -LDH-1 and LDH-2 are predominantly expressed in the heart, kidneys, and erythrocytes, LDH-4 and LDH-5 in the liver and skeletal muscle, and LDH isoenzymes of intermediate mobility in spleen, lymph nodes, leukocytes, and platelets [11] . In turn, LDH-3 is prevalent in lung tissue and total serum LDH has been proposed as a tumour biomarker for lung cancer [12] . Severe infections may cause tissue damage induced by cytokine production with subsequent release of LDH into the bloodstream [13] . In this context, it has been proposed [6] that the main LDH isoform in lung tissue, LDH-3, could be released in greater amounts in the more severely affected patients with COVID-19, since a severe form of interstitial pneumonia (often evolving into acute respiratory distress syndrome) is the hallmark of this disease [14] . However, to our best knowledge, the contribution of the different LDH isoenzymes to the total LDH elevation that is usually observed in COVID-19 has not been determined. It was the purpose of this study to evaluate whether the plasma profile of the different LDH isoenzymes is altered in patients with COVID-19 compared with controls, and whether this is associated with a specific elevation of LDH-3. This study was approved by the Institutional Review Board of "12 de Octubre" University Hospital of Madrid (Spain) (No. #20/222). We obtained fresh plasma aliquots from supernatants of peripheral blood samples collected in lithium heparinized tubes that were previously centrifuged for 10 min at 1500xg in our Emergency/Core Laboratoryof note, there is not an optimal storage condition for all LDH isoenzymes [15] and preserving frozen samples can destroy the activity of some LDH isoenzymes activity [11] . We selected patients diagnosed with COVID-19 using real-time reverse transcription polymerase chain reaction within four days after hospital admission. Eligibility was based on their total plasma LDH activity with the aim of covering a wide range of elevated levels in LDH activities, and on their clinical and laboratory data in order to obtain a mixed study sample regarding the COVID-19 severity [3, 16] (Table 1) . Patient's plasma LDH activities ranged from 281 to 822 U/L. Seven control fresh plasma aliquots were obtained from blood samples belonging to adult (> 50-year-old) outpatients attending our center, who had no symptoms suggestive of COVID19 and showed normal values of total LDH activities (<230 U/L, range 112 -194 U/L). Total plasma LDH was measured by an optimized standardized method of the Clinical Chemistry German Society [17] in a Cobas 8000 Modular Autoanalyzer (Roche diagnostics, Basel, Switzerland) which measures the initial oxidation rate of NADH in the reaction between pyruvate and NADH to form L-lactate and NAD + catalysed by LDH. Samples with 'haemolysis index' > 5 (as calculated by the autoanalyzer) were discarded to prevent false elevations in plasma LDH activity due in vitro haemolysis. The five plasma LDH isoenzymes were separated by electrophoresis in agarose gel using the SAS-1 LD Vis Kit in the SAS-1 Plus instrument (Helena Biosciences Europe, UK) that uses a modification of the method described by Preston et al. [18] to detect the J o u r n a l P r e -p r o o f LDH activity (i.e., in-gel oxidation of Lactate to Pyruvate by LDH is detected with a colorimetric reagent containing lactate as a substrate, NAD+ as an acceptor of electrons, and staining by a tetrazolium salt). LDH-1 isoenzyme runs anodic and muscle LDH-5 runs cathodic, with intermediate positions for the remainder of heterotetrameric isoenzymes (LDH2-4). Electrophoresis was performed at 80V and 15ºC for 20 minutes following incubation at 45ºC for 25 minutes with the reagents required for the identification of LDH isoenzymes. Electrophoretic bands were relatively quantified by densitometry using Image J freeware program (Figure 1) , and the in-gel relative activity of each LDH isoenzyme was expressed as a percentage of the total in-gel LDH activity. Plasma albumin was measured by an immunoturbidimetric method. Plasma alanine (ALT) and aspartate transaminase (AST) were measured following the IFCC recommendations [19] , creatinine was measured with a colorimetric test based on the Jaffé method [20] , and C-reactive protein (CRP) and ferritin were measured with an immunoturbidimetric test using latex coated particles with monoclonal anti-CRP antibodies and anti-ferritin antibodies, respectively. All these aforementioned measurements were done in a Cobas 8000 Modular Autoanalyzer (Roche Diagnotics). The haematological parameters were assayed in a DxH 900 hematology analyser (Beckman Coulter; Brea, CA). We used the Mann-Whitney U test to compare between patients and controls total LDH activity, as well as the relative activity levels of the different LDH isoenzymes. We used the Spearman correlation to determine the association within the patients' group between the relative activity of the different LDH isoenzymes and total plasma LDH activity, and also between LDH-3 isoenzyme relative activity and some blood/plasma analytes that have been shown to be altered in patients with COVID-19 (i.e., albumin [7, 8] , AST [7, 8] , ALT [7, 8] , creatinine [3, 7, 8] , CRP [4, [7] [8] [9] , ferritin [7, 8, 14] , haemoglobin concentration [7] , leukocyte count and cell subpopulations [4, [7] [8] [9] , and platelet count [7] Data analysis and graphical output were carried out with R (4.0.1) statistical software and the level of statistical significance was set at 0.05. Total LDH activity was significantly higher in patients than in controls (p<0.001). Yet, we found no significant differences between patients and controls for the in-gel relative activity of LDH isoenzymes (all p>0.05, Figure 1 ). In the group of patients no significant correlation were found between plasma total LDH activity (U/L) and the percentage of in-gel activity of the different LDH isoenzymesincluding the predominant form in lungs, LDH3 -(See Supplemental Data Figure S1 ). Likewise, no significant correlations were found between LDH-3 relative activity and the various haematological and serum biochemical parameters we studied (See Figure S2 ). Our results suggest that the plasma LDH elevation that is typically found in patients with COVID19 is not due to a specific increase of the predominant LDH isoenzyme in lungs, LDH-3, in detriment of any other LDH isoenzyme. Indeed, we found no significant differences in LDH-3 levels between patients and controls. Likewise, none of the other LDH isoenzymes analysed seems to be a major contributor to the increase of total plasma LDH levels observed in COVID-19 patients, as we failed to find any correlation between the activity level of the different LDH isoenzymes and total plasma LDH activity. Furthermore, we intended to explore whether LDH-3 relative activity was associated with various blood and plasma parameters that had been previously reported to be altered in patients with COVID-19 [4, [7] [8] [9] , but failed to find any significant correlation. The small cohort of patients is a limitation of the study, but the required use of fresh plasma samples to avoid the loss of LDH isoenzyme activity poses a major problem to schedule the electrophoretic assay [11, 15] . However, we intended to get a representative sample of COVID-19 status, by collecting patients' samples encompassing a range of total LDH activities according to previously reported values in patients with COVID-19 [6] , as well as by selecting patients with a wide spectrum of clinical and laboratory parameters associated with COVID-19 severity [3, 7] (Table 1) . The elevation of plasma LDH activity, a routine laboratory analyte with a promising value for prognostic and stratifying strategies in COVID-19, does not appear to be due to the specific release into bloodstream of the prevalent LDH-3 isoenzyme in lungs as previously suggested [6] . 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