Obesity pharmacotherapy in older adults: a narrative review of evidence
- PMID: 38710803
- PMCID: PMC11971046
- DOI: 10.1038/s41366-024-01529-z
Obesity pharmacotherapy in older adults: a narrative review of evidence
Abstract
The prevalence of obesity in older adults (people aged >60 years) is increasing in line with the demographic shift in global populations. Despite knowledge of obesity-related complications in younger adults (increased risk of type 2 diabetes, liver and cardiovascular disease and malignancy), these considerations may be outweighed, in older adults, by concerns regarding weight-loss induced reduction in skeletal muscle and bone mass, and the awareness of the 'obesity paradox'. Obesity in the elderly contributes to various obesity-related complications from cardiometabolic disease and cancer, to functional decline, worsening cognition, and quality of life, that will have already suffered an age-related decline. Lifestyle interventions remain the cornerstone of obesity management in older adults, with emphasis on resistance training for muscle strength and bone mineral density preservation. However, in older adults with obesity refractory to lifestyle strategies, pharmacotherapy, using anti-obesity medicines (AOMs), can be a useful adjunct. Recent evidence suggests that intentional weight loss in older adults with overweight and obesity is effective and safe, hence a diminishing reluctance to use AOMs in this more vulnerable population. Despite nine AOMs being currently approved for the treatment of obesity, limited clinical trial evidence in older adults predominantly focuses on incretin therapy with glucagon-like peptide-1 receptor agonists (liraglutide, semaglutide, and tirzepatide). AOMs enhance weight loss and reduce cardiometabolic events, while maintaining muscle mass. Future randomised controlled trials should specifically evaluate the effectiveness of novel AOMs for long-term weight management in older adults with obesity, carefully considering the impact on body composition and functional ability, as well as health economics.
© 2024. Crown.
Conflict of interest statement
Competing interests: DJC has received investigator-initiated grants from Astra Zeneca and Novo Nordisk, as well as speaker fees for lectures. UA has received investigator-led grant from Proctor and Gamble, as well as speaker fees for lectures. He has also received honoraria from Boehringer Ingelheim, Eli Lilly, Napp, Proctor and Gamble and Sanofi for educational meetings. JPHW consults widely for pharmaceutical companies in relation to obesity and diabetes (fees paid to the University of Liverpool) and via his institution has received research grants from industry. He is received lecture fees from commercial organisations including the pharmaceutical industry and has provided unpaid support to various charities in relation to his interest in obesity and diabetes. AEH has no conflicts of interest to declare.
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