|Year : 2016 | Volume
| Issue : 1 | Page : 45-50
Efficacy and safety of escitalopram versus desvenlafaxine in the treatment of major depression: A preliminary 1-year prospective randomized open label comparative trial
Brij Mohan Gupta1, Samir H Zargar1, Manu Arora2, Vishal R Tandon1
1 Department of Pharmacology and Therapeutics, Government Medical College, Jammu, Jammu and Kashmir, India
2 Department of Psychiatry, Government Medical College, Jammu, Jammu and Kashmir, India
|Date of Web Publication||12-Jan-2016|
Vishal R Tandon
Department of Pharmacology, Government Medical College, Jammu - 180 001, Jammu and Kashmir
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Aim and Objective: To compare efficacy and safety of escitalopram with desvenlafaxine in the treatment of major depression.Materials and Methods: A total of 60 patients of depression were randomized into two groups after meeting inclusion criterion. In the first 3 weeks, escitalopram 10 mg/day was given and then 20 mg/day for the next 3 weeks in group 1 (n = 30). Desvenlafaxine in the first 3 weeks was given 50 mg/day and 100 mg/day for the next 3 weeks in group 2 (n = 30). The parameters evaluated during the study were efficacy assessments byHamilton Scale of Rating Depression (HAM-D), Hamilton Rating Scale of Anxiety (HAM-A), and Clinical Global Impression (CGI). Safety assessments were done by UKU-scale. Results: Escitalopram and desvenlafaxine significantly (P < 0.001), reduced HAM-D, HAM-A, and CGI scores from their respective base lines. However, on comparison failed show any statistical difference at 3 and 6 weeks of treatment. Escitalopram and desvenlafaxine were both found to be safe and well-tolerated and there was not much difference between the two groups as evident from UKU Scale and their effect on various biochemical parameters. Conclusion: The present study demonstrated similar efficacy and safety in reducing depression and anxiety with both escitalopram and desvenlafaxine, but clinical superiority of one drug over the other cannot be concluded due to limitations of the small sample size.
Keywords: Comparative effectiveness research, observational studies, randomized controlled trials
|How to cite this article:|
Gupta BM, Zargar SH, Arora M, Tandon VR. Efficacy and safety of escitalopram versus desvenlafaxine in the treatment of major depression: A preliminary 1-year prospective randomized open label comparative trial. Perspect Clin Res 2016;7:45-50
|How to cite this URL:|
Gupta BM, Zargar SH, Arora M, Tandon VR. Efficacy and safety of escitalopram versus desvenlafaxine in the treatment of major depression: A preliminary 1-year prospective randomized open label comparative trial. Perspect Clin Res [serial online] 2016 [cited 2020 Jan 22];7:45-50. Available from: http://www.picronline.org/text.asp?2016/7/1/45/173771
| Introduction|| |
Major depressive disorder is a prevalent and disabling illness worldwide, associated with significant impairment in physical and social functioning as well as increased morbidity and mortality. At its worst, depression can lead to suicide. Fewer than 25% of those affected have access to effective treatments. A large selection of effective antidepressant medications is available, but their clinical utility is limited by adverse events or some or other problems. Indeed, the clinical success of the selective serotonin reuptake inhibitors (SSRIs) over the past decade relative to their therapeutic predecessors, such as tricyclic antidepressants, has been attributed to their improved tolerability, ease of use and far greater safety. However, the safety and tolerability of individual SRIs vary within the class  and it is clear that many patients may not respond optimally to an acute course of any given treatment. Thus, there is a constant need of search for new better effective treatment.
The efficacy and the tolerability of escitalopram, aSSRI and desvenlafaxine, a non-selective SRI has been well-established.,,,,,,,,,,,,,,,,, Most of the studies establishing their efficacy and safety are available from western population and whatever available has compared these drugs respectively with placebo. Thus, there are very limited studies available directly comparing efficacies of escitalopram with desvenlafaxine in treatment of major depression.
Hence, a preliminary 1-year prospective randomized open label trial comparing efficacy and safety of escitalopram with desvenlafaxine in the treatment of major depression was undertaken.
| Materials and Methods|| |
A total of 60 patients from psychiatry outpatient departmentof a tertiary level hospital diagnosed with major depression were included in the study after they fulfilled the inclusion criteria. A total of 30 patients were taken in each group. A written informed consent was obtained from first relative after explaining the nature and purpose of the study along with reverse consent from the patients on their clinical improvement was taken. The study was approved by institutional ethics committee, GMC, Jammu vide number 36A/Pharma/IEC/2010/528 dated 27. 10. 2010. The flow diagram of the study is shown in [Figure 1].
Patients with major depression of both sexes in the age group of 18-55 years with a Hamilton Scale of Rating Depression (HAM-D) score >20; who meet Diagnostic and Statistical Manual of Mental Disorders-IV criteria for depression, with a minimum total score of 20 on the 24-item Hamilton Scale for Depression, non pregnant females and without any comorbid conditions like DM, HT, and IHD were included in the study.
“Patients with the following conditions were excluded from the study - those taking any antidepressant in the last 6 weeks; intake of any drug which may causes depressive state, psychosis or anxiety; any chronic ailment; any substance abuse; and those patients intolerant or allergic to the drug.
In case any exacerbation of disease or ADR event during the study, the data from this population were decided to be included in statistical analysis at the time of their exclusion.
Patients meeting eligibility criteria at the screening visit were assigned randomly in 1:1 ratio to either receive escitalopram or desvenlafaxine. The total duration of study was 6 weeks. The dose of study medication was to be increased after 3 weeks in accordance with the approved labelling information. In the first 3 weeks, escitalopram 10 mg/day was given and then 20 mg/day for the next 3 weeks. Dose of desvenlafaxine in the first 3 weeks was 50 mg/day and 100 mg/day for the next 3 weeks. The primary endpoints were HAM-D, Hamilton Rating Scale of Anxiety (HAM), and Clinical Global Impression (CGI).
Adverse event monitoring was done by using UKU-scale. Furthermore, some of biochemical parameter like blood sugar, LFT, and RFT were also analyzed and compared among two treatment arms for safety assessment.
All the analysis was carried out with the help of computer software SPSS version 15 for windows. The evaluation of patients in two groups was done by applying HAM-D, HAM-A, and CGI and will be reported as mean ± standard deviation scores. The score were reported as % change from the baseline and were assessed by use of paired/unpaired “t” test/analysis of covariance whichever was applicable. Categorical variables were reported as percentage and the statistical analysis done by use of Chi-square test. A P < 0.05 was considered statistically significant. All P values reported analyses were two-tailed. The analysis was done on intention-to-treat basis.
| Results|| |
The base line parameters of both the group has been shown in [Table 1]. Both escitalopram as well as desvenlafaxine significantly (P < 0.001) reduced HAM-D, HAM-A, and CGI scores from their respective base lines [Table 2]. However, on comparison failed show any statistical difference at 3 and 6 weeks of treatment [Table 3].
|Table 2: Effect of treatment across escitalopram (n=30) and desvenlafaxine (n=30) groups over time: Scores within subjects (mean±standard deviation)|
Click here to view
|Table 3: Effect of treatment across escitalopram (n=30) and desvenlafaxine (n=30) groups over time: Scores between subjects (mean±standard deviation)|
Click here to view
Escitalopram and desvelafaxine were both safe and well-tolerated and there was not much difference between the two groups as evident from UKU-scale [Table 4].
|Table 4: Effect of escitalopram (n=30) and desvenlafaxine (n=30) On UKU scale at 6 weeks|
Click here to view
Escitalopram and desvelafaxine were both safe and well-tolerated and there was not much difference between the two groups as far the effect on various biochemical parameters was concerned [Table 5].
|Table 5: Effect of escitalopram (n=30) and desvenlafaxine (n=30) on various biochemical parameters (mean±standard deviation)|
Click here to view
Side effects seen in the present study with escitalopram were headache (n = 6), nausea (n = 4), vomiting (n = 1), diarrhea (n = 2), palpitations (n = 3), sexual dysfunction (n = 1), loss of appetite (n = 1), insomnia (n = 3), and constipation (n = 1). Whereas, with desvelafaxine were headache (n = 4), nausea (n = 9), palpitations (n = 2), insomnia (n = 3), constipation (n = 3), giddiness (n = 4), dry mouth (n = 3), and restlessness (n = 1).
| Discussion|| |
In the present study, it was seen that escitalopram-reduced depression levels with a decrease from the baseline value HAM-D from 3 weeks onward till the end of the study. The above findings are in concurrence with various published reports in which these drugs, individually were efficacious in decreasing depression and anxiety in comparison to placebo.
A similar reduction in depression by escitalopram is also reported by Burke et al., and Leopolo et al., who showed that escitalopram significantly improved MADRS scores in comparison to placebo starting with in within one week of treatment and persisting till 8 weeks of therapy at both the doses (10 mg and 20 mg).
Rapaport et al., showed that the time to depression relapse was significantly longer (P = 0.013) and the cumulative rate of relapse was significantly lower in patients who received escitalopram (26%escitalopram vs. 40% placebo; hazard ratio = 0.56; P = 0.01). Moore et al., showed that the Montgomery-Åsberg Depression Rating Scale (MADRS) score decreased more in the escitalopram than in the citalopram arm (–22.4 ± 12.9 vs. –20.3 ± 12.7; P < 0.05). There were more treatment responders with escitalopram (76.1%) than with citalopram (61.3%, P < 0.01).
In the present study, it was seen that desvenlafaxine produced a decrease from the baseline value of HAM-D from 3 weeks onward till the end of the study, that is, at 6 weeks. Desvenlafaxine has also been shown to cause a significant reduction in depression in several studies.,,, These studies found out that mean HAM-D scores for desvenlafaine 50, 100, 200, and 400 mg/day were significantly lower than placebo, respectively.
In the present study, there was a trend toward the higher overall response of escitalopram in decreasing depression and anxiety than with desvenlafaxine (F = 3.014, P = 0.057). Our results are almost in accordance to those put forth by Soares et al., who reported a similar reduction in depression with escitalopram and desvenlafaxine. Reductions in HAM-D17 total score at acute phase end point were similar for desvelafaxine and escitalopram-treated women (-13.6 vs. 14.3, respectively, P = 0.24). No significant difference was observed between groups at continuation phase end points in the proportion of who maintained response (desvenlafaxine, 82%; escitalopram, 80%, P = 0.70).
Limited studies have directly compared the efficacy of escitalopram with desvenlafaxine in treatment of major depression, otherwise escitalopram has been compared with class SNRI's in other studies. Kornstein et al., showed that mean reduction in MADRS score from baseline to week 8 was significantly greater for the escitalopram group versus the SNRI group.
In the present study, it was seen that escitalopram produced a decrease from the baseline value of HAM-A, from 3 weeks onward till the end of the study, that is, at 6 weeks indicating additional antianxiety activity. Similar reductions in anxiety by escitalopram were put forth by Malin et al., who consistently demonstrated significant anxiolytic properties in addition to antidepressant efficacy with escitalopram. It also showed efficacy in treating panic disorder and generalized and social anxiety disorders.
Bandelow et al., documented the efficacy of escitalopram, on symptoms of anxiety in patients with major depressive disorder. Similarly, escitalopram was shown significantly more effective compared to placebo in treating both anxiety symptoms and the entire depression in the total depressive population, as well as in depressive patients with a high degree of anxiety by Cyril and Jaromir.
In the present study, it was seen that desvenlafaxine also produced a decrease from the baseline value of HAM-A, from 3 weeks onward till the end of the study, that is, at 6 weeks. Similar reductions in anxiety by desvenlafaxine were put forth by Tourian et al. In this secondary analysis, desvenlafaxine-treated patients experienced significant improvement in anxiety symptoms compared with placebo-treated patients.
In current study, there is no significant difference in the efficacy of escitalopram and desvenlafaxine in reducing anxiety (F = 2.596, P = 0.083). Similar results are shown by Soares et al., where there are no differences in the efficacy of escitalopram and desvelafaxine in reducing anxiety.
In the present study, it was seen that escitalopram produced a decrease from the respective baseline value of CGI from 3 weeks onward till the end of the study, that is, at 6 weeks. A similar reduction in CGI by escitalopram is also reported by, Olié et al., and Yevtushenko et al.
In the present study, it was seen that desvenlafaxine also produced a decrease from the respective baseline value of CGI from 3 weeks onward till the end of the study, that is, at 6 weeks. Similar reductions in CGI were seen in other studies also.,
In current study, there is no significant difference in the CGI scores of escitalopram group and desvenlafaxine group (P = 0.475) Scores between subjects. Similar results were seen by Soares et al., with almost same reduction in both escitalopram and desvenlafaxine group.
In the present study, escitalopram and desvenlafaxine were safe and well-tolerated. UKU scale is used to evaluate side effects and the values are (0.93 and 1.13), respectively in escitalopram and desvenlafaxine group. There is no statistically significant difference between the two groups (t =0.96, P = 0.33). There was no other discontinuation due to any other reasons including adverse effects in the present study. Similar side effect profile was put forth by Soares et al., who showed both desvenlafaxine and escitalopram were generally safe and well-tolerated.
The present study does have some limitations. First, it is a short-term study with less number of patients andeffect of small sample size cannot be ruled out on results of the study.
| Conclusion|| |
The present study demonstrated almost similar efficacy and safety in reducing depression and anxiety with both escitalopram and desvenlafaxine, but clinical superiority of one drug over the other cannot be definitely be concluded due to small sample size. Escitalopram and desvenlafaxine were well-tolerated.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Murray CJ, Lopez AD. Alternative projections of mortality and disability by cause 1990-2020: Global Burden of Disease Study. Lancet 1997;349:1498-504.
Olver JS, Burrows GD, Norman TR. Third generation antidepressants; do they offer advantages over the SSRI's? CNS Drugs 2001;15:941-54.
Peretti S, Judge R, Hindmarch I. Safety and tolerability considerations: Tricyclic antidepressants vs selective serotonin reuptake inhibitors. Acta Psychiatr Scand Suppl 2000;403:17-25.
American Psychiatric Association, Diagnostic and Statistical Manual of mental Disorders. 4th
ed. Washington: American Psychiatry Association; 1994.
Hamilton M. A rating for depression. J Neurol Neurosurg Psychiatry 1960;23:56-62.
Burke WJ, Gergel I, Bose A. Fixed-dose trial of the single isomer SSRI escitalopram in depressed outpatients. J Clin Psychiatry 2002;63:331-6.
Leopolo UM, Loft H, Reines EH. Escitalopram (10–20 mg/day) is effective and well tolerated in a placebo-controlled study in depression in primary care. Int Clin Psychopharmacol 2003;18:211-7.
Rapaport MH, Bose A, Zheng H. Escitalopram continuation treatment prevents relapse of depressive episodes. J Clin Psychiatry 2004;65:44-9.
Moore N, Verdoux H, Fantino B. Prospective, multicentre, randomized, double-blind study of the efficacy of escitalopram versus citalopram in outpatient treatment of major depressive disorder”. Int Clin Psychopharmacol 2005;20:131-7.
DeMartinis NA, Yeung P, Entsuah R, Manley AL. A double blind placebo-controlled study of the efficacy and safety of desvenlafaxine succinate in the treatment of major depressive disorder. J Clin Psychiatry 2007;68:677-88.
Septien-Veleza L, Pitroskya B, Padmanabhan SK, Germain JM, Tourian KA. A randomized, double-blind, placebo-controlled trial of desvenlafaxine succinate in the treatment of major depressive disorder. Int Clin Psychopharmacol 2007;22:338-47.
Liebowitz MR, Manley AL, Padmanandan SK, Ganguly R, Tummala R, Tourian KA. Efficacy, safety, and tolerability of desvenlafaxine 50mg/day and 100mg/day in outpatients with major depressive disorder. Cur Med Res Opin 2008;24:1877-90.
Boyer P, Montgomery SA, Lepola U, Germain JM, Brisard C, Ganguly R, et al.
Efficacy, safety, and tolerability of fixed-dose desvenlafaxine 50 and 100 mg/day for major depressive disorder in a placebo-controlled trial. Int Clin Psychopharmacol 2008;23:243-53.
Soares CN, Thase ME, Clayton A, Guico-Pabia CJ, Focht K, Jiang Q, et al.
Desvenlafaxine and escitalopram for the treatment of postmenopausal women with major depressive disorder. Menopause 2010;17:700-11.
Kornstein SG, Bose A, Dayongli, Saikali KG, Gandhi C. Escitalopram maintenance treatment for prevention of recurrent depression: A randomized, placebo-controlled trial. J Clin Psychiatry 2006;67:1767-75.
Malin PJ, Wengel, SP, Burke WJ. Escitalopram: Better treatment for depression is through the looking glass. Expert Rev Neurother 2004;4:769-79.
Bandelow B, Andersen HF, Dolberg OT. Escitalopram in the treatment of anxiety symptoms associated with depression. Depress Anxiety 2007;24:53-61.
Höschl C, Svestka J. Escitalopram for the treatment of major depression and anxiety disorders. Expert Rev Neurother 2008;8:537-52.
Tourian KA, Jiang Q, Ninan PT. Analysis of the effect of desvenlafaxine on anxiety symptoms associated with major depressive disorder. Pooled Data from 9 short- term, double –blind, placebo-controlled trials. CNS Spectra 2010;15:187-93.
Olié JP, Tonnoir B, Ménard F, Galinowski A. A prospective study of escitalopram in the treatment of major depressive episodes in the presence or absence of anxiety. Depress Anxiety 2007;24:318-24.
Yevtushenko VY, Belous AI, Yevgenia G. Efficacy and tolerability of escitalopram versus citalopram in major depressive disorder: A 6-week, multicenter, prospective, randomized, double-blind, active-controlled study in adult outpatients. Clin Ther 2007;29:2319-32.
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5]
|This article has been cited by|
||Efficacy and safety of escitalopram in treatment of severe depression in Chinese population
| ||Tianmei Si,Gang Wang,Fude Yang,Yiru Fang,Maosheng Fang,Jijun Li,Jicheng Dong,Xinhua Shen,Jianmin Zhuo,Qing Rui,Jinan Wang,Hu Cuili |
| ||Metabolic Brain Disease. 2017; 32(3): 891 |
|[Pubmed] | [DOI]|