Evidence map›Paper›PMID 28601891›Full record

Trial reportJAMA psychiatry2017

Effect of Liraglutide Treatment on Prediabetes and Overweight or Obesity in Clozapine- or Olanzapine-Treated Patients With Schizophrenia Spectrum Disorder: A Randomized Clinical Trial.

Julie R Larsen, Louise Vedtofte, Mathilde S L Jakobsen, Hans R Jespersen, Michelle I Jakobsen, Camilla K Svensson, Kamuran Koyuncu, Ole Schjerning, Peter S Oturai, Andreas Kjaer and 6 more

Registry-linked trialAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in JAMA psychiatry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01845259 (Does a GLP-1 Receptor Agonist Change Glucose Tolerance in Antipsychotic-treated Patients? A Randomized, Double-blinded, Placebo-controlled Clinical Trial), which is not on this map. Cited by 92 papers, 9 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed, 9 pooled it
10.1field-weighted citation impact, top 1% 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.

NCT01845259 phase2unknown statusnot on this map

Does a GLP-1 Receptor Agonist Change Glucose Tolerance in Antipsychotic-treated Patients? A Randomized, Double-blinded, Placebo-controlled Clinical Trial

TypeinterventionalSponsorPsychiatric Centre RigshospitaletRan2013 to 2017Enrolled103ConditionsImpaired Glucose Tolerance Associated With DrugsArmsLiraglutide, Liraglutide Placebo
3 · Its place in the literature

Who cites it

92 citing papers in PubMed, 9 syntheses or guidelines pooled it, 213 citations in OpenAlex.

  1. Efficacy of Weight-Lowering Agents on Fat Distribution: A Systematic Review and Network Meta-Analysis of Randomized Controlled Trials.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2026
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32 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 8 institutions in 2 countries.

Julie R LarsenPsychiatric Centre, University of Copenhagen, Copenhagen, Denmark2currently with Novo Nordisk A/S, Bagsværd, Denmark.
Louise VedtofteCenter for Diabetes Research, Gentofte Hospital, University of Copenhagen, Copenhagen, Denmark.
Mathilde S L JakobsenPsychiatric Centre, University of Copenhagen, Copenhagen, Denmark.
Hans R JespersenPsychiatric Centre, University of Copenhagen, Copenhagen, Denmark.
Michelle I JakobsenPsychiatric Centre, University of Copenhagen, Copenhagen, Denmark.
Camilla K SvenssonPsychiatric Centre, University of Copenhagen, Copenhagen, Denmark.
Kamuran KoyuncuPsychiatric Centre, University of Copenhagen, Copenhagen, Denmark.
Ole SchjerningDepartment of Psychiatry, Aalborg University Hospital, Aalborg University, Aalborg, Denmark.
Peter S OturaiDepartment of Clinical Physiology, Nuclear Medicine and PET, Cluster for Molecular Imaging, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Andreas KjaerDepartment of Clinical Physiology, Nuclear Medicine and PET, Cluster for Molecular Imaging, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Jimmi NielsenDepartment of Psychiatry, Aalborg University Hospital, Aalborg University, Aalborg, Denmark.
Jens J HolstNovo Nordisk Foundation Center for Basic Metabolic Research, Panum Institute, University of Copenhagen, Copenhagen, Denmark7Department of Biomedical Sciences, Panum Institute, University of Copenhagen, Copenhagen, Denmark.
Claus T EkstrømDepartment of Public Health, Section of Biostatistics, University of Copenhagen, Copenhagen, Denmark.
Christoph U CorrellPsychiatry Research, Zucker Hillside Hospital, Northwell Health, Glen Oaks, New York10Department of Psychiatry and Molecular Medicine, Hofstra Northwell School of Medicine, Hempstead, New York11Center for Psychiatric Neuroscience, Feinstein Institute for Medical Research, Manhasset, New York12Department of Psychiatry and Behavioral Sciences, Albert Einstein College of Medicine, Bronx, New York.
Tina VilsbøllCenter for Diabetes Research, Gentofte Hospital, University of Copenhagen, Copenhagen, Denmark13Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Anders Fink-JensenPsychiatric Centre, University of Copenhagen, Copenhagen, Denmark13Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark14Steno Diabetes Center Copenhagen, University of Copenhagen, Copenhagen, Denmark.
University of Copenhagen · DKGentofte Hospital · DKAalborg University · DKAalborg University Hospital · DKFeinstein Institute for Medical Research · USNovo Nordisk (Denmark) · DKRigshospitalet · DKSteno Diabetes Center · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Compared with the general population, patients with schizophrenia have a 2- to 3-fold higher mortality rate primarily caused by cardiovascular disease. Previous interventions designed to counteract antipsychotic-induced weight gain and cardiometabolic disturbances reported limited effects. Objectives: To determine the effects of the glucagon-like peptide-1 receptor agonist liraglutide added to clozapine or olanzapine treatment of schizophrenia spectrum disorders. Design, Setting, and Participants: This randomized clinical double-blind trial enrolled participants at 2 clinical sites in Denmark. Of 214 eligible participants with a schizophrenia spectrum disorder, 103 were randomized to liraglutide or placebo. Participants received stable treatment with clozapine or olanzapine, were overweight or obese, and had prediabetes. Data were collected from May 1, 2013, through February 25, 2016. Interventions: Treatment for 16 weeks with once-daily subcutaneous injection of liraglutide or placebo. Trial drug therapy was titrated during the first 2 weeks of the study. Main Outcomes and Measures: The primary end point was change in glucose tolerance estimated by a 75-g oral glucose tolerance test result. Secondary end points included change in body weight and cardiometabolic parameters. Results: Of the 103 patients undergoing randomization (60 men [58.3%] and 43 women [41.7%]), 97 were included in the efficacy analysis, with a mean (SD) age of 42.5 (10.5) years and mean (SD) body mass index (calculated as weight in kilograms divided by height in meters squared) of 33.8 (5.9). The liraglutide and placebo groups had comparable characteristics (mean [SD] age, 42.1 [10.7] vs 43.0 [10.5] years; 30 men in each group; mean [SD] body mass index, 33.7 [5.1] vs 33.9 [6.6]). A total of 96 randomized participants (93.2%) completed the trial. Glucose tolerance improved in the liraglutide group compared with the placebo group (P < .001). Altogether, 30 liraglutide-treated participants (63.8%) developed normal glucose tolerance compared with 8 placebo-treated participants (16.0%) (P < .001; number needed to treat, 2). Body weight decreased with liraglutide compared with placebo (-5.3 kg; 95% CI, -7.0 to -3.7 kg). Reductions in waist circumference (-4.1 cm; 95% CI, -6.0 to -2.3 cm), systolic blood pressure (-4.9 mm Hg; 95% CI, -9.5 to -0.3 mm Hg), visceral fat (-250.19 g; 95% CI, -459.9 to -40.5 g), and low-density lipoprotein levels (-15.4 mg/dL; 95% CI, -23.2 to -7.7 mg/dL) occurred with liraglutide compared with placebo. Adverse events with liraglutide affected mainly the gastrointestinal tract. Conclusions and Relevance: Liraglutide significantly improved glucose tolerance, body weight, and cardiometabolic disturbances in patients with schizophrenia spectrum disorders treated with clozapine or olanzapine. Trial Registration: clinicaltrials.gov Identifier: NCT01845259.

Indexed as

Glucagon-Like Peptide-1 Receptor AgonistsOutcome Assessment, Health CareAdultAntipsychotic AgentsBenzodiazepinesClozapineDouble-Blind MethodFemaleHumansHypoglycemic AgentsLiraglutideMaleMiddle AgedObesityOlanzapineOverweightAntipsychotic AgentsBenzodiazepinesClozapineGlucagon-Like Peptide-1 Receptor AgonistsHypoglycemic AgentsLiraglutideOlanzapine

Identifiers

PMID28601891
PMCPMC5710254
OpenAlexW2621462012

What OpenQuestion holds

Texttitle and abstract
Read underepoch 390

Registered trials

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.