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Agomelatine for the Treatment of Generalized Anxiety Disorder: A Meta-Analysis

OBJECTIVE: Despite multiple drugs available, a large proportion of patients with generalized anxiety disorder (GAD) do not show adequate response and remission. Thus, additional novel pharmacological agents are needed to increase treatment option for GAD. We aimed to investigate efficacy and safety...

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Autores principales: Wang, Sheng-Min, Woo, Young Sup, Kim, Nak-Young, Na, Hae-Ran, Lim, Hyun Kook, Bahk, Won-Myong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean College of Neuropsychopharmacology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7383014/
https://www.ncbi.nlm.nih.gov/pubmed/32702221
http://dx.doi.org/10.9758/cpn.2020.18.3.423
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author Wang, Sheng-Min
Woo, Young Sup
Kim, Nak-Young
Na, Hae-Ran
Lim, Hyun Kook
Bahk, Won-Myong
author_facet Wang, Sheng-Min
Woo, Young Sup
Kim, Nak-Young
Na, Hae-Ran
Lim, Hyun Kook
Bahk, Won-Myong
author_sort Wang, Sheng-Min
collection PubMed
description OBJECTIVE: Despite multiple drugs available, a large proportion of patients with generalized anxiety disorder (GAD) do not show adequate response and remission. Thus, additional novel pharmacological agents are needed to increase treatment option for GAD. We aimed to investigate efficacy and safety of agomelatine in the treatment of GAD by conducting a meta-analysis. METHODS: An extensive search of multiple databases and clinical trial registries were conducted. Mean change in total scores on Hamilton Anxiety Rating Scale (HAM-A) from baseline to endpoint was our primary outcome measure. Secondary efficacy measures included response and remission rates, as defined by a 50% or greater reduction in HAM-A total scores and a score of 7 or less in HAM-A total scores at study endpoint respectively. RESULTS: Four published double blinded, randomized, placebo-controlled trials were included in this meta-analysis. Agomelatine more significantly (standardized mean difference = −0.56, p = 0.004) improved HAM-A total scores than placebo. The odds ratios (ORs) of agomelatine over placebo for response and remission rates were 3.75 (p < 0.00001) and 2.74 (p < 0.00001), respectively. Agomelatine was generally well tolerated with insignificance in dropout rate, somnolence, headache, nasopharyngitis, and dizziness compared with placebo. However, agomelatine showed significantly higher incidence of liver function increment (OR = 3.13, p = 0.01) and nausea (OR = 3.27, p = 0.02). CONCLUSION: We showed that agomelatine may be another treatment option in patients with GAD. However, the results should be interpreted and translated into clinical practice with caution because the meta-analysis was based on limited numbers of clinical trials.
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spelling pubmed-73830142020-08-31 Agomelatine for the Treatment of Generalized Anxiety Disorder: A Meta-Analysis Wang, Sheng-Min Woo, Young Sup Kim, Nak-Young Na, Hae-Ran Lim, Hyun Kook Bahk, Won-Myong Clin Psychopharmacol Neurosci Original Article OBJECTIVE: Despite multiple drugs available, a large proportion of patients with generalized anxiety disorder (GAD) do not show adequate response and remission. Thus, additional novel pharmacological agents are needed to increase treatment option for GAD. We aimed to investigate efficacy and safety of agomelatine in the treatment of GAD by conducting a meta-analysis. METHODS: An extensive search of multiple databases and clinical trial registries were conducted. Mean change in total scores on Hamilton Anxiety Rating Scale (HAM-A) from baseline to endpoint was our primary outcome measure. Secondary efficacy measures included response and remission rates, as defined by a 50% or greater reduction in HAM-A total scores and a score of 7 or less in HAM-A total scores at study endpoint respectively. RESULTS: Four published double blinded, randomized, placebo-controlled trials were included in this meta-analysis. Agomelatine more significantly (standardized mean difference = −0.56, p = 0.004) improved HAM-A total scores than placebo. The odds ratios (ORs) of agomelatine over placebo for response and remission rates were 3.75 (p < 0.00001) and 2.74 (p < 0.00001), respectively. Agomelatine was generally well tolerated with insignificance in dropout rate, somnolence, headache, nasopharyngitis, and dizziness compared with placebo. However, agomelatine showed significantly higher incidence of liver function increment (OR = 3.13, p = 0.01) and nausea (OR = 3.27, p = 0.02). CONCLUSION: We showed that agomelatine may be another treatment option in patients with GAD. However, the results should be interpreted and translated into clinical practice with caution because the meta-analysis was based on limited numbers of clinical trials. Korean College of Neuropsychopharmacology 2020-08-31 2020-08-31 /pmc/articles/PMC7383014/ /pubmed/32702221 http://dx.doi.org/10.9758/cpn.2020.18.3.423 Text en Copyright © 2020, Korean College of Neuropsychopharmacology This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Wang, Sheng-Min
Woo, Young Sup
Kim, Nak-Young
Na, Hae-Ran
Lim, Hyun Kook
Bahk, Won-Myong
Agomelatine for the Treatment of Generalized Anxiety Disorder: A Meta-Analysis
title Agomelatine for the Treatment of Generalized Anxiety Disorder: A Meta-Analysis
title_full Agomelatine for the Treatment of Generalized Anxiety Disorder: A Meta-Analysis
title_fullStr Agomelatine for the Treatment of Generalized Anxiety Disorder: A Meta-Analysis
title_full_unstemmed Agomelatine for the Treatment of Generalized Anxiety Disorder: A Meta-Analysis
title_short Agomelatine for the Treatment of Generalized Anxiety Disorder: A Meta-Analysis
title_sort agomelatine for the treatment of generalized anxiety disorder: a meta-analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7383014/
https://www.ncbi.nlm.nih.gov/pubmed/32702221
http://dx.doi.org/10.9758/cpn.2020.18.3.423
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