Metformin for Clozapine Associated Obesity: A Systematic Review and Meta-Analysis

PLoS One. 2016 Jun 15;11(6):e0156208. doi: 10.1371/journal.pone.0156208. eCollection 2016.

Abstract

Background: Although clozapine is the gold-standard for treatment refractory schizophrenia, it has the worst metabolic profile of all antipsychotics. This is partly mediated by clozapine's impact on glucagon-like peptide (GLP-1). There is an absence of robust evidence for effective treatments for clozapine associated weight gain and metabolic syndrome. Metformin, with its role in increasing GLP-1 may aid weight loss among people on clozapine.

Methods: We conducted a systematic-review and meta-analysis of metformin versus placebo for change in weight and metabolic syndrome for people on clozapine without diabetes mellitus. We searched the Cochrane Schizophrenia Group's trial register, Pubmed and Embase, as well as the following Chinese databases: the Chinese Biomedical Literature Service System and China Knowledge Resource Integrated Database. This was supplemented by hand searches of key papers.

Results: Eight studies, of which three were from Chinese databases, with 478 participants were included. We found that metformin was superior to placebo in terms of weight loss (-3.12kg, 95%CI -4.88kg to -1.37kg) and BMI (-1.18kg/m2, 95%CI -1.76kg/m2 to -0.61kg/m2). Metformin significantly improved three of the five components of metabolic syndrome; waist circumference, fasting glucose and triglycerides. Sensitivity analysis on study quality and duration did not greatly impact results.

Conclusions: Metformin led to clinically meaningful weight loss among people on clozapine, and may reduce the rates of metabolic syndrome. Inclusion of metformin into the treatment protocols of people on clozapine, as tolerated, should be considered.

Trial registration: PROSPERO registration number: CRD42015029723.

Publication types

  • Meta-Analysis
  • Review
  • Systematic Review

MeSH terms

  • Antipsychotic Agents / adverse effects
  • Blood Glucose / metabolism
  • Body Mass Index
  • Body Weight / drug effects
  • Clozapine / adverse effects
  • Fasting / blood
  • Humans
  • Hypoglycemic Agents / therapeutic use
  • Metabolic Syndrome / blood
  • Metabolic Syndrome / prevention & control
  • Metformin / therapeutic use*
  • Obesity / chemically induced
  • Obesity / drug therapy*
  • Randomized Controlled Trials as Topic
  • Schizophrenia / drug therapy
  • Treatment Outcome
  • Triglycerides / blood
  • Waist Circumference / drug effects
  • Weight Gain / drug effects*

Substances

  • Antipsychotic Agents
  • Blood Glucose
  • Hypoglycemic Agents
  • Triglycerides
  • Metformin
  • Clozapine

Grants and funding

The authors received an Intra-Faculty Collaborative Workshop grant from the University of Queensland School of Medicine which covered the open access publication costs of this manuscript. DS is funded in part through an NHMRC ECF (APP1111136).