4.6 Editorial Material

Giving weight to incretin-based pharmacotherapy for obesity-related sleep apnea: a revolution or a pipe dream?

期刊

SLEEP
卷 -, 期 -, 页码 -

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/sleep/zsad224

关键词

OSA; obesity; OSA - pharmacotherapy; endocrinology; OSA - endocrine morbidity/interactions; weight management; incretins; weight loss

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Obesity is a chronic disease that affects over 670 million adults globally, leading to complications such as obstructive sleep apnea (OSA). Weight loss in patients with obesity-related OSA can effectively improve their condition, surpassing the benefits of device-based OSA therapies. Incretin-based pharmacotherapies have shown promising results in reducing weight and improving metabolic health, and ongoing trials are examining their efficacy in individuals with obesity-related OSA.
Obesity is a chronic disease affecting over 670 million adults globally, with multiple complications including obstructive sleep apnea (OSA). Substantial weight loss in patients with obesity-related OSA can reduce or even eliminate OSA as well as reduce sleepiness and improve cardio-metabolic health. Evidence suggests that these improvements exceed those that occur with device-based OSA therapies like continuous positive airway pressure which continue to be the first-line of therapy. Resistance to weight management as a first-line strategy to combat OSA could arise from the complexities in delivering and maintaining adequate weight management, particularly in sleep clinic settings. Recently, incretin-based pharmacotherapies including glucagon-like peptide 1 (GLP-1) receptor agonists alone or combined with glucose-dependent insulinotropic polypeptide (GIP) receptor agonists have been developed to target glycemic control in type 2 diabetes. These medications also slow gastric emptying and reduce energy intake. In randomized, placebo-controlled trials of these medications in diabetic and non-diabetic populations with obesity, participants on active medication lost up to 20% of their body weight, with corresponding improvements in blood pressure, lipid levels, physical functioning, and fat mass loss. Their adverse effects are predominantly gastrointestinal-related, mild, and transient. There are trials currently underway within individuals with obesity-related OSA, with a focus on reduction in weight, OSA severity, and cardio-metabolic outcomes. These medications have the potential to substantially disrupt the management of OSA. Pending coming data, we will need to consider pharmacological weight loss as a first-line therapy and how that influences training and management guidelines.

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