Evidence map›Paper›PMID 34727399›Full record

SynthesisHuman psychopharmacology2021

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

Caroline Zangani, Barbara Giordano, Hans-Christian Stein, Stefano Bonora, Armando D'Agostino, Edoardo Giuseppe Ostinelli

Erratum issuedOpen access · hybridAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Human psychopharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. ENX-104: a selective and potent DNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  5. Review
  6. Article
  7. Review
  8. Corrigendum.Human psychopharmacology · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Caroline ZanganiOxford Health NHS Foundation Trust, Warneford Hospital, Oxford, UK.ORCID 0000-0001-5883-0638
Barbara GiordanoDepartment of Health Sciences, University of Milan, Milan, Italy.ORCID 0000-0001-9262-079X
Hans-Christian SteinDepartment of Health Sciences, University of Milan, Milan, Italy.ORCID 0000-0002-3662-1752
Stefano BonoraDepartment of Health Sciences, University of Milan, Milan, Italy.
Armando D'AgostinoDepartment of Health Sciences, University of Milan, Milan, Italy.ORCID 0000-0002-2126-799X
Edoardo Giuseppe OstinelliOxford Health NHS Foundation Trust, Warneford Hospital, Oxford, UK.ORCID 0000-0002-8717-0832
University of Milan · ITOxford Health NHS Foundation Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDepressive 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.

methodsWe 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.

resultsWe 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

conclusionTreatment 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.

Indexed as

Antipsychotic AgentsMajor Depressive DisorderAmisulprideDepressionDysthymic DisorderHumansAmisulprideAntipsychotic Agentsantipsychoticsdepressiondysthymiaschizofrenia

Identifiers

PMID34727399
PMCPMC8596405
OpenAlexW3169964830

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.