Literature DB >> 23472671

A pooled analysis of six month comparative efficacy and tolerability in four randomized clinical trials: agomelatine versus escitalopram, fluoxetine, and sertraline.

Koen Demyttenaere1, Emanuelle Corruble, Anthony Hale, Maria-Antonia Quera-Salva, Françoise Picarel-Blanchot, Siegfried Kasper.   

Abstract

OBJECTIVE: A pooled-analysis on the long-term outcome in four head-to-head studies: agomelatine versus fluoxetine, sertraline, and (twice) escitalopram. Method A meta-analytic approach was used. Hamilton Depression Rating Scale (HAM-D) scores, response and remission rates, Clinical Global Impression of Improvement (CGI-I) scores, response and remission rates, and completion rates/discontinuation rates due to adverse events were analyzed.
RESULTS: At the last post-baseline assessment on the 24-week treatment period, the final HAM-D-17 score was significantly lower in patients treated with agomelatine than in patients treated with selective serotonin reuptake inhibitors (SSRIs), as well in the total group of patients with severe depression (P = 0.014 and 0.040, respectively). HAM-D response rates at the end of 24 weeks were significantly higher in patients treated with agomelatine than in patients treated with SSRIs, as well in the total group of patients with severe depression (P = 0.031 and 0.048, respectively). HAM-D remission rates at the end of 24 weeks were numerically but not significantly higher in patients treated with agomelatine than in patients treated with SSRIs. Final CGI-I scores were significantly lower for agomelatine. CGI-I response as well as remission rates were numerically higher in patients treated with agomelatine, without statistical significance. The percentage of patients with at least one emergent adverse event leading to treatment discontinuation was 9.4% in patients treated with SSRIs and 6.6% in patients treated with agomelatine (P = 0.065).
CONCLUSION: The present pooled analysis shows that, from a clinical point of view, agomelatine is at least as efficacious as the investigated SSRIs with a trend to fewer discontinuations due to adverse events.

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Year:  2013        PMID: 23472671     DOI: 10.1017/S1092852913000060

Source DB:  PubMed          Journal:  CNS Spectr        ISSN: 1092-8529            Impact factor:   3.790


  7 in total

Review 1.  Agomelatine: an agent against anhedonia and abulia?

Authors:  J Thome; P Foley
Journal:  J Neural Transm (Vienna)       Date:  2013-12-06       Impact factor: 3.575

2.  A systematic review of agomelatine-induced liver injury.

Authors:  Silka Dawn Freiesleben; Karolina Furczyk
Journal:  J Mol Psychiatry       Date:  2015-04-21

3.  Agomelatine versus Sertraline: An Observational, Open-labeled and 12 Weeks Follow-up Study on Efficacy and Tolerability.

Authors:  Esma Akpınar; Cem Cerit; Anıl Talas; Ümit Tural
Journal:  Clin Psychopharmacol Neurosci       Date:  2016-11-30       Impact factor: 2.582

4.  Agomelatine in the treatment of mild-to-moderate depression in patients with cardiovascular disease: results of the national multicenter observational study PULSE.

Authors:  Vladimir E Medvedev
Journal:  Neuropsychiatr Dis Treat       Date:  2017-04-21       Impact factor: 2.570

Review 5.  Antidepressant efficacy of agomelatine: meta-analysis of published and unpublished studies.

Authors:  David Taylor; Anna Sparshatt; Seema Varma; Olubanke Olofinjana
Journal:  BMJ       Date:  2014-03-19

Review 6.  Efficacy and tolerability of agomelatine in the treatment of depression.

Authors:  Blanka Kores Plesničar
Journal:  Patient Prefer Adherence       Date:  2014-05-02       Impact factor: 2.711

7.  Characterisation of Agomelatine-Induced Increase in Liver Enzymes: Frequency and Risk Factors Determined from a Pooled Analysis of 7605 Treated Patients.

Authors:  Gabriel Perlemuter; Patrice Cacoub; Dominique Valla; Dominique Guyader; Barbara Saba; Cécile Batailler; Kevin Moore
Journal:  CNS Drugs       Date:  2016-09       Impact factor: 5.749

  7 in total

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