Efficacy of amisulpride for depressive symptoms in individuals with mental disorders: A systematic review and meta-analysis.


Journal

Human psychopharmacology
ISSN: 1099-1077
Titre abrégé: Hum Psychopharmacol
Pays: England
ID NLM: 8702539

Informations de publication

Date de publication:
11 2021
Historique:
received: 04 03 2021
accepted: 15 05 2021
entrez: 2 11 2021
pubmed: 3 11 2021
medline: 16 3 2022
Statut: ppublish

Résumé

Depressive symptoms occur in several psychiatric disorders, often in the absence of a formal diagnosis of depression. We aimed to evaluate the efficacy and the tolerability of amisulpride, both alone and as augmentation therapy, in the treatment of depressive symptoms in individuals with any major psychiatric disorder. We searched PubMed, Embase, PsycINFO, GreyLit, OpenGrey and ProQuest up to March 2020 for randomised controlled trials focussing on the treatment of an acute depressive episode in any major psychiatric disorder. A random-effect meta-analysis was performed to synthesize the findings on depressive symptoms (primary outcome), response rate and tolerability. We retrieved 11 studies including 2065 patients with a diagnosis of dysthymia (eight studies), major depression (one study) or schizophrenia (two studies). Amisulpride 50 mg/day was associated with a larger reduction of depressive symptoms compared to placebo (standardised mean difference [SMD] = -0.70, CI 95% -0.92, -0.49; I Treatment with amisulpride could be a valid choice for selected individuals with dysthymia or depressive symptoms in the context of schizophrenia. More studies on the efficacy and tolerability of amisulpride are needed to draw firm conclusions on its potential benefits in other psychiatric disorders.

Sections du résumé

BACKGROUND
Depressive symptoms occur in several psychiatric disorders, often in the absence of a formal diagnosis of depression. We aimed to evaluate the efficacy and the tolerability of amisulpride, both alone and as augmentation therapy, in the treatment of depressive symptoms in individuals with any major psychiatric disorder.
METHODS
We searched PubMed, Embase, PsycINFO, GreyLit, OpenGrey and ProQuest up to March 2020 for randomised controlled trials focussing on the treatment of an acute depressive episode in any major psychiatric disorder. A random-effect meta-analysis was performed to synthesize the findings on depressive symptoms (primary outcome), response rate and tolerability.
RESULTS
We retrieved 11 studies including 2065 patients with a diagnosis of dysthymia (eight studies), major depression (one study) or schizophrenia (two studies). Amisulpride 50 mg/day was associated with a larger reduction of depressive symptoms compared to placebo (standardised mean difference [SMD] = -0.70, CI 95% -0.92, -0.49; I
CONCLUSION
Treatment with amisulpride could be a valid choice for selected individuals with dysthymia or depressive symptoms in the context of schizophrenia. More studies on the efficacy and tolerability of amisulpride are needed to draw firm conclusions on its potential benefits in other psychiatric disorders.

Identifiants

pubmed: 34727399
doi: 10.1002/hup.2801
pmc: PMC8596405
doi:

Substances chimiques

Antipsychotic Agents 0
Amisulpride 8110R61I4U

Types de publication

Journal Article Meta-Analysis Review Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2801

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2021 The Authors. Human Psychopharmacology: Clinical and Experimental published by John Wiley & Sons Ltd.

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Auteurs

Caroline Zangani (C)

Oxford Health NHS Foundation Trust, Warneford Hospital, Oxford, UK.
Department of Psychiatry, University of Oxford, Oxford, UK.
Oxford Precision Psychiatry Lab, NIHR Oxford Health Biomedical Research Centre, Oxford, UK.
Department of Health Sciences, University of Milan, Milan, Italy.

Barbara Giordano (B)

Department of Health Sciences, University of Milan, Milan, Italy.

Hans-Christian Stein (HC)

Department of Health Sciences, University of Milan, Milan, Italy.

Stefano Bonora (S)

Department of Health Sciences, University of Milan, Milan, Italy.

Armando D'Agostino (A)

Department of Health Sciences, University of Milan, Milan, Italy.

Edoardo Giuseppe Ostinelli (EG)

Oxford Health NHS Foundation Trust, Warneford Hospital, Oxford, UK.
Department of Psychiatry, University of Oxford, Oxford, UK.
Oxford Precision Psychiatry Lab, NIHR Oxford Health Biomedical Research Centre, Oxford, UK.

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