GLP-1 receptor agonist treatment increases bone formation and prevents bone loss in weight-reduced obese women

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Abstract

Context: Recent studies indicate that glucagon-like peptide (GLP)-1 regulates bone turnover, but the effects of GLP-1 receptor agonists (GLP-1 RAs) on bone in obese weight-reduced individuals are unknown. Objective: To investigate the role of GLP-1 RAs on bone formation and weight loss-induced bone mass reduction. Design: Randomized control study. Setting: Outpatient research hospital clinic. Participants: Thirty-seven healthy obese women with body mass index of 34 ± 0.5 kg/m2 and age 46 ± 2 years. Intervention: After a low-calorie-diet-induced 12% weight loss, participants were randomized to treatment with or without administration of the GLP-1 RA liraglutide (1.2 mg/d) for 52 weeks. In case of weight gain, up to two meals per day could be replaced with a low-calorie-diet product to maintain the weight loss. Main Outcome Measures: Total, pelvic, and arm-leg bone mineral content (BMC) and bone markers [C-terminal telopeptide of type 1 collagen (CTX-1) and N-terminal propeptide of type 1 procollagen (P1NP)] were investigated before and after weight loss and after 52-week weight maintenance. Primary endpoints were changes in BMC and bone markers after 52-week weight maintenance with or without GLP-1 RA treatment. Results: Total, pelvic, and arm-leg BMC decreased during weight maintenance in the control group (P < .05). The bone resorption marker CTX-1 collagen did not change during the weight loss maintenance phase. Conclusions: Treatment with a long-acting GLP-1 RA increased bone formation by 16% and prevented bone loss after weight loss obtained through a low-calorie diet, supporting its role as a safe weight-lowering agent.

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APA

Iepsen, E. W., Lundgren, J. R., Hartmann, B., Pedersen, O., Hansen, T., Jørgensen, N. R., … Torekov, S. S. (2015). GLP-1 receptor agonist treatment increases bone formation and prevents bone loss in weight-reduced obese women. Journal of Clinical Endocrinology and Metabolism, 100(8), 2909–2917. https://doi.org/10.1210/jc.2015-1176

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