Combination of exercise and GLP-1 receptor agonist treatment reduces severity of metabolic syndrome, abdominal obesity, and inflammation: a randomized controlled trial

Rasmus M Sandsdal, Christian R Juhl, Simon B K Jensen, Julie R Lundgren, Charlotte Janus, Martin B Blond, Mads Rosenkilde, Adrian F Bogh, Lasse Gliemann, Jens-Erik B Jensen, Charalambos Antoniades, Bente M Stallknecht, Jens J Holst, Sten Madsbad, Signe S Torekov

27 Citations (Scopus)

Abstract

Background: Identifying and reducing cardiometabolic risks driven by obesity remains a healthcare challenge. The metabolic syndrome is associated with abdominal obesity and inflammation and is predictive of long-term risk of developing type 2 diabetes and cardiovascular disease in otherwise healthy individuals living with obesity. Therefore, we investigated the effects of adherent exercise, a glucagon-like peptide 1 receptor agonist (GLP-1 RA), or the combination on severity of metabolic syndrome, abdominal obesity, and inflammation following weight loss. Methods: This was a randomized, double-blinded, placebo-controlled trial. During an 8-week low-calorie diet (800 kcal/day), 195 adults with obesity and without diabetes lost 12% in body weight. Participants were then evenly randomized to four arms of one-year treatment with: placebo, moderate-to-vigorous exercise (minimum of 150 min/week of moderate-intensity or 75 min/week of vigorous-intensity aerobic physical activity or an equivalent combination of both), the GLP-1 RA liraglutide 3.0 mg/day, or a combination (exercise + liraglutide). A total of 166 participants completed the trial. We assessed the prespecified secondary outcome metabolic syndrome severity z-score (MetS-Z), abdominal obesity (estimated as android fat via dual-energy X-ray absorptiometry), and inflammation marker high-sensitivity C-reactive protein (hsCRP). Statistical analysis was performed on 130 participants adherent to the study interventions (per-protocol population) using a mixed linear model. Results: The diet-induced weight loss decreased the severity of MetS-Z from 0.57 to 0.06, which was maintained in the placebo and exercise groups after one year. MetS-Z was further decreased by liraglutide (− 0.37, 95% CI − 0.58 to − 0.16, P < 0.001) and the combination treatment (− 0.48, 95% CI − 0.70 to − 0.25, P < 0.001) compared to placebo. Abdominal fat percentage decreased by 2.6, 2.8, and 6.1 percentage points in the exercise, liraglutide, and combination groups compared to placebo, respectively, and hsCRP decreased only in the combination group compared with placebo (by 43%, P = 0.03). Conclusion: The combination of adherent exercise and liraglutide treatment reduced metabolic syndrome severity, abdominal obesity, and inflammation and may therefore reduce cardiometabolic risk more than the individual treatments. Trial registration EudraCT number: 2015-005585-32, ClinicalTrials.gov:

Original languageEnglish
Article number41
JournalCardiovascular Diabetology
Volume22
Issue number1
ISSN1475-2840
DOIs
Publication statusPublished - Dec 2023

Keywords

  • Adult
  • Humans
  • Liraglutide/therapeutic use
  • Glucagon-Like Peptide-1 Receptor/agonists
  • Diabetes Mellitus, Type 2/drug therapy
  • Obesity, Abdominal/complications
  • Metabolic Syndrome/drug therapy
  • C-Reactive Protein
  • Obesity/epidemiology
  • Weight Loss
  • Exercise
  • Inflammation/complications
  • Double-Blind Method
  • Obesity
  • GLP-1
  • Randomized clinical trial
  • Cardiometabolic risk
  • Inflammation
  • Metabolic syndrome

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