Glucagon-like peptide-1 agonists combating clozapine-associated obesity and diabetes

Karla Mayfield, Dan Siskind, Karl Winckel, Anthony W. Russell, Steve Kisely, Greg Smith, Samantha Hollingworth

Research output: Contribution to journalReview ArticleResearchpeer-review

35 Citations (Scopus)

Abstract

Clozapine is the most effective antipsychotic, but its use is tempered by adverse metabolic effects such as weight gain, glucose intolerance and type II diabetes. Current interventions do not facilitate compelling or sustained improvement in metabolic status. Recent studies suggest that glucagon-like peptide-1 (GLP-1) may play a key role in clozapine's metabolic effects, possibly suggesting that clozapine-associated obesity and diabetes are mediated independently through reduced GLP-1. As a result, GLP-1 agonists could show promise in reversing antipsychotic-induced metabolic derangements, providing mechanistic justification that they may represent a novel approach to treat, and ultimately prevent, both diabetes and obesity in patients on clozapine. GLP-1 agonists are already used for diabetes, and they provide a unique combination of glycaemic improvement and metabolically relevant weight loss in diabetic and non-diabetic patients, in the context of a currently favourable safety proifile. Using GLP-1 agonists for clozapine-associated obesity and diabetes could be a potentially effective intervention that may reduce cardiometabolic morbidity and mortality in this vulnerable patient population.

Original languageEnglish
Pages (from-to)227-236
Number of pages10
JournalJournal of Psychopharmacology
Volume30
Issue number3
DOIs
Publication statusPublished - Mar 2016
Externally publishedYes

Keywords

  • antipsychotic
  • Clozapine
  • GLP-1
  • metabolic
  • schizophrenia

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