Karakasis Paschalis, Sagris Marios, Patoulias Dimitrios, Koufakis Theocharis, Theofilis Panagiotis, Klisic Aleksandra, Fragakis Nikolaos, El Tanani Mohamed, Rizzo Manfredi
Second Department of Cardiology, Hippokration General Hospital, Aristotle University of Thessaloniki, 54642 Thessaloniki, Greece.
First Cardiology Department, School of Medicine, Hippokration General Hospital, National and Kapodistrian University of Athens, 15772 Athens, Greece.
Biomedicines. 2024 Nov 1;12(11):2503. doi: 10.3390/biomedicines12112503.
Obstructive sleep apnea (OSA) is a prevalent condition associated with increased cardiovascular risk, particularly in individuals with comorbid obesity and type 2 diabetes (T2D). Despite the widespread use of continuous positive airway pressure (CPAP) for OSA management, adherence remains suboptimal, and CPAP has not consistently demonstrated reductions in surrogate cardiovascular events. Recently, attention has focused on glucagon-like peptide-1 receptor agonists (GLP-1RAs) and sodium-glucose cotransporter-2 (SGLT2) inhibitors as potential therapeutic agents for mitigating cardiovascular risk in OSA patients. These agents, originally developed for T2D management, have demonstrated pleiotropic effects, including significant weight loss, blood pressure reduction, and amelioration of endothelial dysfunction and arterial stiffness, along with anti-inflammatory benefits, which may be particularly beneficial in OSA. Emerging clinical evidence suggests that GLP-1RAs and SGLT2 inhibitors can reduce OSA severity and improve daytime sleepiness, potentially reversing the adverse cardiovascular effects observed in OSA. This review explores the pathophysiological mechanisms linking OSA with cardiovascular disease and evaluates the potential therapeutic roles of GLP-1RAs and SGLT2 inhibitors in addressing cardiovascular risk in OSA patients. Further research, including long-term clinical trials, is necessary to establish the effectiveness of these therapies in reducing cardiovascular events and improving patients' reported outcomes in this population.
阻塞性睡眠呼吸暂停(OSA)是一种常见病症,与心血管疾病风险增加相关,尤其是在合并肥胖症和2型糖尿病(T2D)的个体中。尽管持续气道正压通气(CPAP)广泛用于OSA的治疗,但依从性仍然欠佳,而且CPAP并未始终如一地显示出能降低替代心血管事件的发生率。最近,胰高血糖素样肽-1受体激动剂(GLP-1RAs)和钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂作为减轻OSA患者心血管疾病风险的潜在治疗药物受到了关注。这些最初用于治疗T2D的药物已显示出多效性作用,包括显著的体重减轻、血压降低、内皮功能障碍和动脉僵硬度改善,以及抗炎益处,这在OSA中可能特别有益。新出现的临床证据表明,GLP-1RAs和SGLT2抑制剂可以降低OSA的严重程度并改善日间嗜睡,有可能逆转OSA中观察到的不良心血管影响。本综述探讨了将OSA与心血管疾病联系起来的病理生理机制,并评估了GLP-1RAs和SGLT2抑制剂在解决OSA患者心血管疾病风险方面的潜在治疗作用。需要进一步的研究,包括长期临床试验,以确定这些疗法在降低心血管事件发生率和改善该人群患者报告结局方面的确切效果。