key: cord-0029405-3p1fe4o7
authors: Ch, Saritha; Sudha, Sree; Reddy, C. Gowtham; T, Pugazhenthan; KSBS, Krishna Sasanka; Dasari, Pooja; Battula, Pradeep; T, Nandini; A, Sandeep
title: A Comparative Study on Safety and Efficacy of Desvenlafaxine Versus Sertraline in Depression
date: 2022-02-28
journal: nan
DOI: 10.7759/cureus.22717
sha: 7a9253248ea4965d545bb5cb016a6713556a19f6
doc_id: 29405
cord_uid: 3p1fe4o7

Background Depression is one of the most predominant mental health issues that are prevalent now. Therefore, many clinical trials were being conducted to find the safest, most effective, and tolerable anti-depressant. This study aims to compare desvenlafaxine and sertraline regarding their safety and efficacy in treating depression. Methodology The patients who were diagnosed with depressive disorder according to the Diagnostic and Statistical Manual of Mental Disorders (DSM-5) criteria were included in the study and were divided into two groups. The severity of depression in these patients was evaluated using Beck Depression Inventory and Hamilton depression scale (HAM-D) before and after the treatment (four weeks). Results About 64% of the study sample were males, and 36% were females, with 77% of the patients in the desvenlafaxine group taking 100 mg dosage and about 74% patients taking 50 mg dosage in the sertraline group. The patients in both groups showed statistically significant (p < 0.00001) improvement after using these drugs. Conclusion Both desvenlafaxine and sertraline showed their efficacy in treating depression by improving the clinical outcome in patients. Sertraline was marginally better in clinical results. Finally, it is advisable to carry out more randomized trials to improve the patient’s quality of life.

In a person's lifetime, the estimated occurrence of at least one episode of major depressive disorder is about 17% [1] . This occurrence causes psychiatrists and physicians to encounter this disorder often in their clinics. Patients suffering from depression not only experience difficulties in their social functioning but also have impaired work output [2] [3] . All this has led to the recognition of depression as the fourth most leading disability globally [4] . It has been established that the primary choice in the management of depression is pharmacotherapy [5] . Antidepressants are also used to treat chronic pain, which can result in depression [6] [7] . The prescriptions for treating depression mainly include second-generation antidepressants like selective serotonin reuptake inhibitors (SSRIs), serotonin and norepinephrine reuptake inhibitors (SNRIs), and other drugs that selectively target neurotransmitters [8] . SSRIs are also combined with antipsychotics to treat bipolar depression [9] . Depression is most commonly treated in three divided stages -acute, continuation, and maintenance phases [10] . From the presentation of symptoms to eliciting a clinical response comprises the acute phase. It has now been recommended to have at least six months of continuation therapy. In the maintenance phase, the psychiatrist aims to prevent the occurrence of another episode [11] [12] .

The improved safety and tolerability of SSRIs and SNRIs caused them to gain popularity in treating depression over the older tricyclic antidepressants [13] . Sertraline belongs to SSRIs which inhibit only serotonin reuptake. At the same time, desvenlafaxine has dual-acting properties as it can block the reuptake of serotonin and norepinephrine and belongs to SNRIs [14] [15] . It has been found that there is dysregulation of serotonin and norepinephrine neurotransmitter systems in patients suffering from depression [16] . 1 2 1 3 4 5 5 5 5 Evidence has been established regarding the safety of sertraline in the maintenance therapy of depression in various placebo-controlled trials [17] .

The third SNRI that the US FDA has approved for the treatment of depression is desvenlafaxine (administered as desvenlafaxine succinate) [18] . It has been derived from SNRI venlafaxine in a salt form of its isolated major active metabolite (O-desmethylvenlafaxine). Research regarding the use of desvenlafaxine for patients suffering from major depressive disorder has been thorough. The safety, efficacy, and tolerability of desvenlafaxine have been established by many double-blind, placebo-controlled, multicentric, and randomized trials [19] . Furthermore, the effective relieving of painful symptoms linked to major depressive disorder has been confirmed with the use of desvenlafaxine by numerous clinical trials when compared with placebo [20] [21] [22] . Unfortunately, there is a paucity in the literature for comparative studies between sertraline and desvenlafaxine, especially in rural populations. Several studies have established the safety and efficacy of these drugs compared to placebo; however, the edge of one drug over another in terms of patient's clinical response is yet to be established. The main aim of this study is to find out a better drug profile between sertraline and desvenlafaxine in relation to their safety, efficacy, and tolerability by patients suffering from a major depressive disorder.

A prospective observational study was carried out comparing the efficacy and tolerability of sertraline to desvenlafaxine in treating depression. This study was conducted at Santhiram Medical College and General Hospital, Nandyal, for a duration of six months from December 2020 to May 2021. The total sample size in this study was 81 patients. The level of depression in these patients was evaluated using Beck Depression Inventory and Hamilton depression scale (HAM-D) before and after the treatment (four weeks). The study was carried out after getting approval from the Institutional Human Ethics Committee (I.E.C./2020/080 dated 22nd December 2020), and after taking written informed consent from patients. The study was carried out from a semi-urban location, with most patients hailing from rural backgrounds. Patients enrolled in this research were divided into two groups based on a simple random sampling procedure. This study included physically healthy outpatients aged between 18 and 75 years diagnosed with depression and met the Diagnostic and Statistical Manual of Mental Disorders (DSM-5) criteria for depressive disorder. Patients hypersensitive to desvenlafaxine and sertraline or with a significant risk of suicide or suffering from depression due to general medical, neurological conditions, pregnant and breastfeeding women, and those not willing to participate in the study were excluded. Figure 1 shows the gender distribution of the patients enrolled in the study according to their age group. Out of the 81 patients in this study, 52 were males, and 29 were females. The majority of the patients (29.6%) were found to be equally distributed in the age groups of 35-45 years and 25-35 years group. They were followed by 21 patients (26%) in the 15-25 years age group. Figure 3 shows the levels of depression among both groups. The levels of depression among the patients who were treated with desvenlafaxine before the treatment were 12 (39.7%), 10 (25.64%), and 17 (43.58%) with minimal depression, moderate depression, severe depression, respectively. However, the levels of depression among the patients who were treated with desvenlafaxine after the treatment were 20 (51.28%), 11 (28.20%), and 8 (20.51%) with normal, minimal depression, and moderate depression, respectively.

The levels of depression among the patients who were treated with sertraline before the treatment were 12 (29.26%), 8 (19.51%), and 22 (53.65%) with minimal depression, moderate depression, and severe depression, respectively. On the other hand, the levels of depression among the patients who were treated with sertraline after the treatment were 25 (60.97%), 14 (34.14%), and 3 (7.31%) with normal, minimal depression, and moderate depression, respectively.

One of the main areas in the field of research related to depression is an attempt to find an effective, tolerable antidepressant based on the patient's characteristics like tolerability, response, and minimal side effects. In the present study, a comparison was carried out between desvenlafaxine and sertraline to assess how they affect the depression of patients. About 64% (52) of the study population were males, and 36% (29) were females, indicating a slight male preponderance towards depression. This variability in the results might be due to the exclusion of gender-specific risk factors like pregnancy and breastfeeding women from this study. This was in contrast with a survey by Kessler RC et al. (1994) , where 13% women versus 8% men had major depression in a twelve-month period in the United States. The authors concluded that females were approximately 1.7 times more likely to suffer from depression when compared with males [22] . However, in a systematic review carried out by Abate KH regarding the gender disparity in the prevalence of depression among the patient population, the author concluded that depression was more common among females than in males [23] . The patients enrolled in the current study were mostly (29.6%) from 35-45 and 25-35 years age groups, followed by 26% in the 15-25 years age bracket. In a placebo-controlled, randomized trial carried out by Lewis G et al. about the effectiveness of sertraline in depression, the majority (41%) of the patients belonged to the age group of 18-34 years, followed by 35-54 years (40%) [24] . This difference in the age distribution might be due to the dissimilarity between the sample size of the studies. Anyhow, studies by Bagby RM et al. [25] and Gartlehner G et al. [8] showed that there was no influence of age on clinical response. The patients in both the groups were given the required dosage of drugs based on their clinical response at the time of follow up, with the majority (77%) of them in the desvenlafaxine group having a dosage of 100 mg and about 74% of the patients in sertraline group taking 50 mg dose. These results differed from Mahajan SS et al., where they calculated the mean dose of escitalopram and desvenlafaxine given to postmenopausal women with anxiety and depression [26] . Lieberman DZ and Massey SH carried out a review about the place of desvenlafaxine in the treatment of major depression and compared its safety and efficacy with other drugs. They found that the dose of 100 mg was well tolerated and safe when compared to a placebo in an eight-week double-blind trial [27] . The disparity in the results with the current study is due to the usage of higher doses of the drug, comparison with other drugs, placebo, and greater sample size. The findings in this study regarding the mean score achieved by the patients in both the groups prior to treatment on the HAM-D and Beck Depression Inventory were similar with a mean of 17 and 25, respectively. Post-treatment, the HAM-D and Beck Depression Inventory mean in the desvenlafaxine group was 9.5 and 16, respectively. While the post-treatment sertraline group showed an improvement by scoring a mean of 8.6 and 14.8 on HAM-D and Beck Depression Inventory, respectively. From this, we can infer that the sertraline group showed a slight margin of improvement in their symptoms compared to that of the desvenlafaxine group. Lustman PJ et al., in their double-blinded, placebo-controlled, randomized trial with sertraline for prevention of depression, used the HAM-D and Beck Depression Inventory at baseline and at random in the first four months of treatment. They found the mean score at baseline on Beck Depression Inventory and HAM-D to be 21.7 ± 6.8 and 15.7 ± 4.9 in the sertraline group, respectively. After four months of treatment, the mean scores were 4.4 ± 3 and 3.3 ± 2.7 on the Beck Depression Inventory and HAM-D, respectively [28] . The variation in the mean scores of the current study and the placebo-controlled trial may be due to the larger sample size and a different study design.

In this study, about 39 patients in the desvenlafaxine group before treatment had minimal, moderate, and severe levels of depression. After taking treatment with desvenlafaxine, they showed improvement, with 20 patients being normal followed by 11 patients with minimal depression. About 42 patients in the sertraline group had minimal, moderate, and severe levels of depression previous to their treatment. Subsequent to their treatment with sertraline, about 25 patients were normal, followed by 13 patients with minimal depression. From the above results, we can gather that patients in the sertraline group showed a better clinical response when compared to those in the desvenlafaxine group. The present study has several limitations in the form of a smaller sample size with samples collected from a single institution with results not generalizable to the whole population. In addition, the duration of observation was at baseline and then four weeks after the onset of treatment. This is a shortcoming as some patients may show better antidepressant response at 6-8 weeks after treatment. Another drawback of this study was that the adverse effects of these drugs were not monitored. Selection bias of the study subjects could be avoided by randomization, which we recommend for future studies.

Both sertraline and desvenlafaxine showed efficacy in treating depression and were well-tolerated as indicated by the application of the HAM-D and Beck Depression Inventory, meeting the hypothesis given by the author. Sertraline showed a better clinical outcome when compared to desvenlafaxine in the present study. This study helps in comparing the drug one on one, unlike the previous studies where the two groups were compared and helps in adding to the current literature. However, a larger randomized comparative clinical trial is recommended to establish the superior efficacy and tolerability of these drugs. 

Human subjects: Consent was obtained or waived by all participants in this study. Santhiram Medical College and General Hospital issued approval I.E.C./2020/080. Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.

Lifetime and 12-month prevalence of DSM-III-R psychiatric disorders in the United States. Results from the National Comorbidity Survey

The functioning and well-being of depressed patients. Results from the medical outcomes study

Functioning and well-being outcomes of patients with depression compared with chronic general medical illnesses

Global mortality, disability, and the contribution of risk factors: Global Burden of Disease Study

National patterns in antidepressant medication treatment

Antidepressant in the treatment of chronic pain: a case report of adult-onset still's disease

Chronic pediatric pain and mental illness during the COVID-19 era: a case series from inpatient child psychiatry unit

Comparative benefits and harms of second-generation antidepressants for treating major depressive disorder: an updated meta-analysis

Bipolar affective disorder. StatPearls [Internet

Long-term treatment of depression

Evidence-based guidelines for treating depressive disorders with antidepressants: a revision of the 1993 British Association for Psychopharmacology guidelines

Pharmacotherapy of depressive disorders. A consensus statement. WHO Mental Health Collaborating Centres

American Medical Association: Awareness, diagnosis, and treatment of depression

Efficacy, safety, and tolerability of desvenlafaxine 50 mg/day and 100 mg/day in outpatients with major depressive disorder

Comparison of sertraline and nortriptyline in the treatment of major depressive disorder in late life

Maintenance phase efficacy of sertraline for chronic depression: a randomized controlled trial

Desvenlafaxine 50 and 100 mg/d in the treatment of major depressive disorder: an 8-week, phase III, multicenter, randomized, double-blind, placebo-controlled, parallel-group trial and a post hoc pooled analysis of three studies

A randomized, double-blind, placebo-controlled trial of desvenlafaxine succinate in adult outpatients with major depressive disorder

A double-blind, placebo-controlled study of the efficacy and safety of desvenlafaxine succinate in the treatment of major depressive disorder

A randomized, double-blind, placebo-controlled trial of desvenlafaxine succinate in the treatment of major depressive disorder

Sex and depression in the National Comorbidity Survey I: Lifetime prevalence, chronicity and recurrence

Gender disparity in prevalence of depression among patient population: a systematic review

The clinical effectiveness of sertraline in primary care and the role of depression severity and duration (PANDA): a pragmatic, double-blind, placebo-controlled randomised trial

Psychosocial and clinical predictors of response to pharmacotherapy for depression

Comparative efficacy and safety of escitalopram versus desvenlafaxine in postmenopausal women with depression and anxiety: a randomized, open-label, comparative trial

Desvenlafaxine in major depressive disorder: an evidence-based review of its place in therapy

Sertraline for prevention of depression recurrence in diabetes mellitus: a randomized, double-blind, placebo-controlled trial