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阻塞性睡眠呼吸暂停异质性与心血管疾病。

Obstructive sleep apnoea heterogeneity and cardiovascular disease.

机构信息

Division of Sleep and Circadian Disorders, Brigham and Women's Hospital, Boston, MA, USA.

Harvard Medical School, Boston, MA, USA.

出版信息

Nat Rev Cardiol. 2023 Aug;20(8):560-573. doi: 10.1038/s41569-023-00846-6. Epub 2023 Mar 10.

DOI:10.1038/s41569-023-00846-6
PMID:36899115
Abstract

Obstructive sleep apnoea (OSA), characterized by recurrent periods of upper airway obstruction and intermittent hypoxaemia, is prevalent in patients with cardiovascular disease (CVD), and is therefore important to consider in the prevention and management of CVD. Observational studies indicate that OSA is a risk factor for incident hypertension, poorly controlled blood pressure, stroke, myocardial infarction, heart failure, cardiac arrhythmias, sudden cardiac death and all-cause death. However, clinical trials have not provided consistent evidence that treatment with continuous positive airway pressure (CPAP) improves cardiovascular outcomes. These overall null findings might be explained by limitations in trial design and low levels of adherence to CPAP. Studies have also been limited by the failure to consider OSA as a heterogeneous disorder that consists of multiple subtypes resulting from variable contributions from anatomical, physiological, inflammatory and obesity-related risk factors, and resulting in different physiological disturbances. Novel markers of sleep apnoea-associated hypoxic burden and cardiac autonomic response have emerged as predictors of OSA-related susceptibility to adverse health outcomes and treatment response. In this Review, we summarize our understanding of the shared risk factors and causal links between OSA and CVD and emerging knowledge on the heterogeneity of OSA. We discuss the varied mechanistic pathways that result in CVD that also vary across subgroups of OSA, as well as the potential role of new biomarkers for CVD risk stratification.

摘要

阻塞性睡眠呼吸暂停(OSA)的特征是上呼吸道反复阻塞和间歇性低氧血症,在心血管疾病(CVD)患者中较为常见,因此在 CVD 的预防和管理中需要考虑到这一点。观察性研究表明,OSA 是高血压、血压控制不佳、中风、心肌梗死、心力衰竭、心律失常、心源性猝死和全因死亡的一个危险因素。然而,临床试验并没有提供一致的证据表明持续气道正压通气(CPAP)治疗可以改善心血管结局。这些总体上的阴性结果可能是由于试验设计的局限性和 CPAP 依从性低所导致的。研究也受到限制,无法将 OSA 视为一种由多种亚型组成的异质性疾病,这些亚型是由解剖学、生理学、炎症和肥胖相关危险因素的不同贡献引起的,从而导致不同的生理紊乱。新型睡眠呼吸暂停相关低氧负荷和心脏自主神经反应的标志物已成为预测 OSA 相关不良健康结局和治疗反应的易感性的指标。在这篇综述中,我们总结了我们对 OSA 和 CVD 之间共同危险因素和因果关系的理解,以及 OSA 异质性的新认识。我们讨论了导致 CVD 的不同机制途径,这些途径也因 OSA 的亚组而异,以及新的生物标志物在 CVD 风险分层中的潜在作用。

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