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Effects of weight-loss interventions on bone health in people living with obesity

医学 减肥 骨质疏松症 骨重建 肥胖 内科学 心理干预 热卡限制 利拉鲁肽 不利影响 健骨 内分泌学 生理学 过度消费 骨密度 骨小梁评分 骨病 低热量饮食 骨矿物 体重增加 卡路里 骨折 骨量减少 恶病质 物理疗法 峰值骨量 骨密度保护剂 骨科手术 外科 体重管理 生物信息学
作者
Julien Paccou,Claudia Gagnon,Elaine W Yu,Clifford J. Rosen
出处
期刊:Journal of Bone and Mineral Research [Oxford University Press]
卷期号:40 (12): 1319-1331 被引量:7
标识
DOI:10.1093/jbmr/zjaf135
摘要

Strategies to reduce weight in people living with obesity (PwO) include calorie restriction, metabolic and bariatric surgery (MBS), and anti-obesity drugs, including glucagon-like peptide-1 receptor agonists (GLP-1Ra). Although weight loss in PwO has many health benefits, it can result in increased bone loss and fracture risk. Indeed, the consequences of weight loss interventions are well known: (1) significant weight loss induced by caloric restriction and MBS results in high turnover bone loss and (2) unlike calorie restriction, PwO experience a substantial deterioration in bone microarchitecture and strength associated with an increased risk of fracture after MBS, especially malabsorptive procedures. GLP-1 may enhance bone metabolism and improve bone quality, and liraglutide appears to have a positive effect on bone health despite significant weight loss in several rodent models. However, most of the positive effects on bone have been observed at concentrations much higher than those approved for obesity care in humans. The effects of GLP-1Ra on bone health in PwO are still limited; however, significant weight loss induced by GLP-1Ra may also result in accelerated bone turnover and bone loss, and semaglutide could lead to an increased risk of fractures in the at-risk population. The mechanisms responsible for the adverse skeletal effects of MBS are not yet fully understood, and there are insufficient human studies supporting pathophysiological hypotheses. However, data suggest that multiple mechanisms are involved, including nutritional factors, mechanical unloading, hormonal factors, adipokines, and alterations in the gut microbiome. Recommendations for the prevention and treatment of osteoporosis secondary to MBS are now available, and the efficacy of anti-osteoporosis medications in preventing bone loss has been evaluated in two randomized controlled trials. Priorities for future research include the development of effective approaches to reduce fracture risk in PwO following MBS and investigation of the effects of anti-obesity drugs on bone health.
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