Evidence map›Paper›PMID 40998755›Full record

SynthesisNeuropsychopharmacology reports2025

Does Adjuvant Metformin Reduce Olanzapine-Induced Metabolic Adverse Effects in Patients Diagnosed With Schizophrenia.

Aquib Butt, Soban Sadiq

Abstract readSystematic Review
In one paragraph

Synthesis in Neuropsychopharmacology reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Aquib ButtKent and Medway Medical School, University of Kent, Canterbury, UK.ORCID https://orcid.org/0009-0001-2740-9944
Soban SadiqKent and Medway Medical School, University of Kent, Canterbury, UK.ORCID https://orcid.org/0009-0008-9016-1807

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOlanzapine is an atypical antipsychotic used in the treatment of schizophrenia, bipolar disorder, and major depressive disorder. In comparison to conventional antipsychotics, it demonstrates superiority in binding to serotonin 5HT-2A than to dopamine D2 receptors, thus presenting as an alternative in having lower extrapyramidal side effects. However, over time, it has become clear that olanzapine carries other prominent adverse effects associated with its use. These relate to the endocrine system and include body weight gain, increased adiposity, insulin resistance, and dyslipidaemia, all of which contribute to metabolic syndrome. Several studies included in this review involved patients with these broader psychiatric diagnoses, not only schizophrenia. This systematic review, therefore, assesses the evidence for the effectiveness of utilizing adjuvant metformin to reduce olanzapine-induced metabolic adverse effects across these populations.

methodsDue to the heterogeneity in available data, this systematic review was conducted via a narrative synthesis method. Initially, the search question was formulated utilizing the PICO tool, then a rigorous search strategy was applied to four search engines. Utilizing the PRISMA flow diagram for visualization of the flow of articles, the initial search revealed a total of 71 articles, whereby strict inclusion and exclusion criteria were applied, revealing the final six articles included in the review. Detailed analysis of the articles allowed key themes and outcomes to be drawn upon, including body weight/BMI, waist circumference, glucose/insulin level changes, and lipid profile. This allowed key data to be grouped and narratively analyzed, resulting in the confident formulation of conclusions regarding the ability of metformin to reduce the metabolic adverse effects of olanzapine.

resultsThrough this review, adjunctive metformin was shown to play a role in reducing metabolic adverse effects associated with olanzapine. Most notably, its positive effect in reducing weight gain/BMI, triglycerides, liver fat content, and insulin resistance-all of which contribute to metabolic syndrome. Furthermore, the addition of metformin was shown to have no impact on waist circumference and certain lipid parameters such as LDL and total cholesterol, warranting further research. However, employing this evidence in the production of guidelines to benefit patients with schizophrenia remains a challenge due to the lack of evidence in the form of randomized controlled trials surrounding the dose-dependent effects, as well as age and gender differences of metformin on olanzapine therapy.

conclusionMetformin addition to olanzapine therapy showed variable effects on some metabolic parameters such as waist circumference and certain lipid parameters. However, it did show consistent effects in managing body weight/BMI, insulin resistance, triglycerides, and liver fat content. This conforms to previous but limited evidence surrounding the use of metformin in reducing metabolic adverse effects of olanzapine therapy. Based on evidence gaps, this review also proposes areas of additional research and offers recommendations, including the use of longer RCTs, larger demographics to determine if the data can be extrapolated to a wider population, and the use of varying doses to ascertain the dose-dependent effects of metformin in alleviating metabolic adverse effects associated with olanzapine therapy.

trial registrationPROSPERO registration ID: CRD420251015966.

Indexed as

Antipsychotic AgentsHypoglycemic AgentsMetabolic DiseasesMetabolic SyndromeMetforminOlanzapineSchizophreniaHumansAntipsychotic AgentsHypoglycemic AgentsMetforminOlanzapineadjunctive therapymetabolic adverse effectsmetforminolanzapineschizophrenia

Identifiers

PMID40998755
PMCPMC12463546

What Socratic holds

Texttitle and abstract
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 Socratic graph.