Respiratory Effects of Treatment with a Glucagon-Like Peptide-1 Receptor Agonist in Patients Suffering from Obesity and Chronic Obstructive Pulmonary Disease

Int J Chron Obstruct Pulmon Dis. 2022 Feb 22:17:405-414. doi: 10.2147/COPD.S350133. eCollection 2022.

Abstract

Purpose: Chronic obstructive pulmonary disease (COPD) affects millions of people worldwide. Obesity is commonly seen concomitantly with COPD. People with COPD have reduced quality of life, reduced physical activity, chronic respiratory symptoms, and may suffer from frequent clinical exacerbations. Liraglutide is a glucagon-like peptide-1 receptor agonist (GLP-1RA) approved for weight loss and treatment of type-2 diabetes mellitus. In addition, liraglutide exerts anti-inflammatory actions by reducing IL-6 and MCP-1 levels. We investigated the effect of liraglutide on pulmonary function in people suffering from obesity and COPD.

Patients and methods: In this controlled, double-blind trial, 40 people with obesity and COPD from two outpatient clinics were allocated randomly to receive liraglutide (3.0 mg, s.c.) or placebo (s.c.) for 40 weeks. At baseline and after 4, 20, 40, and 44 weeks, participants underwent pulmonary-function tests, 6-min walking test, and replied to a questionnaire regarding the clinical impact of COPD (COPD assessment test (CAT)-score).

Results: Compared with placebo, liraglutide use resulted in significant weight loss, increased forced vital capacity (FVC) and carbon monoxide diffusion capacity, and improved CAT-score. We found no significant changes in forced expiratory volume in one second (FEV1), FEV1/FVC, or 6-min walking distance.

Conclusion: In patients suffering from obesity and COPD, 40 weeks of treatment with liraglutide improved some measures of pulmonary function. Our study suggests that liraglutide at 3.0 mg may be appropriate treatment in patients with obesity and COPD.

Keywords: COPD; GLP-1 RA; inflammation; obesity; spirometry.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Forced Expiratory Volume
  • Glucagon-Like Peptide-1 Receptor*
  • Humans
  • Obesity / complications
  • Obesity / diagnosis
  • Obesity / drug therapy
  • Pulmonary Disease, Chronic Obstructive* / diagnosis
  • Pulmonary Disease, Chronic Obstructive* / drug therapy
  • Quality of Life

Substances

  • Glucagon-Like Peptide-1 Receptor

Grants and funding

Study medication and running costs were provided by Novo Nordisk as a part of the Investigator Sponsored Studies Program. We also had financial support from Karola Jørgensens Forskningsfond, Research Council of Hospital South West Jutland, University Hospital of Southern Denmark, and Region of Southern Denmark.