Xu Ding, Zhang Yuekun, Zhen Lei, Hao Wen, Zheng Wen, Yan Yan, Wang Xiao, Nie Shaoping
Center for Coronary Artery Disease, Division of Cardiology, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Cardiometabolic Medicine Center, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Sleep Breath. 2025 Mar 8;29(1):119. doi: 10.1007/s11325-025-03281-8.
Obstructive sleep apnea (OSA) is a recognized cardiovascular risk factor, yet the benefits of intervention remain uncertain due to the heterogeneity among OSA patients. We aimed to explore the association of OSA with cardiovascular outcomes in acute coronary syndrome (ACS) patients with dual risk of elevated remnant cholesterol (RC) and low-grade inflammation indicated by high-sensitivity C-reactive protein (hs-CRP).
This study is a post-hoc analysis of OSA-ACS project enrolled 1833 ACS patients from January 2015 to December 2019, who underwent a sleep study, categorized into four groups by median levels of RC and hs-CRP: RC and low-grade inflammation risk (RCIR), low-grade inflammation risk (LDIR), RC risk (RCR), and no residual risk. The primary endpoint was major adverse cardiovascular and cerebrovascular events (MACCE) including cardiovascular death, myocardial infarction, stroke, hospitalization for unstable angina or heart failure, and ischemia-driven revascularization. Cox proportional hazards models were used to assess the association between OSA and cardiovascular events.
After a median follow-up of 35.13 months, OSA significantly increased the risk of MACCE (adjusted hazard ratio [HR] 1.58, 95% confidence interval [CI] 1.01-2.47; p = 0.045) and stroke (adjusted HR 5.23, 95% CI 1.19-22.99; p = 0.027) in the RCIR group. In the RCIR group, the log-transformed AHI (Log-AHI) and ODI (Log-ODI) were both significantly associated with an increased risk of MACCE, with adjusted hazard ratios of 1.711 (95% CI: 1.092-2.679; p = 0.019) and 1.813 (95% CI: 1.039-3.163; p = 0.036), respectively. Moreover, log-transformed nadir SaO2 (Log-Nadir SaO2) demonstrated a significant inverse association with MACCE risk (adjusted HR: 0.033; 95% CI: 0.001-0.769; p = 0.034).
OSA is prevalent and more severe in ACS patients with dual risk of elevated RC and low-grade inflammation, significantly increasing MACCE and stroke risk, highlighting the need for routine screening and comprehensive management to reduce cardiovascular risk.
阻塞性睡眠呼吸暂停(OSA)是一种公认的心血管危险因素,但由于OSA患者之间存在异质性,干预的益处仍不明确。我们旨在探讨OSA与急性冠状动脉综合征(ACS)患者心血管结局之间的关联,这些患者同时存在残余胆固醇(RC)升高和高敏C反应蛋白(hs-CRP)所提示的低度炎症双重风险。
本研究是对2015年1月至2019年12月纳入的1833例ACS患者的OSA-ACS项目进行的事后分析,这些患者接受了睡眠研究,根据RC和hs-CRP的中位数水平分为四组:RC和低度炎症风险(RCIR)、低度炎症风险(LDIR)、RC风险(RCR)和无残余风险。主要终点是主要不良心血管和脑血管事件(MACCE),包括心血管死亡、心肌梗死、中风、因不稳定型心绞痛或心力衰竭住院以及缺血驱动的血运重建。采用Cox比例风险模型评估OSA与心血管事件之间的关联。
在中位随访35.13个月后,OSA显著增加了RCIR组发生MACCE的风险(调整后风险比[HR]1.58,95%置信区间[CI]1.01-2.47;p = 0.045)和中风风险(调整后HR 5.23,95%CI 1.19-22.99;p = 0.027)。在RCIR组中,对数转换后的呼吸暂停低通气指数(Log-AHI)和氧减指数(Log-ODI)均与MACCE风险增加显著相关,调整后风险比分别为1.711(95%CI:1.092-2.679;p = 0.019)和1.813(95%CI:1.039-3.163;p = 0.036)。此外,对数转换后的最低血氧饱和度(Log-Nadir SaO2)与MACCE风险呈显著负相关(调整后HR:0.033;95%CI:0.001-0.769;p = 0.034)。
在具有RC升高和低度炎症双重风险的ACS患者中,OSA普遍存在且更为严重,显著增加MACCE和中风风险,凸显了进行常规筛查和综合管理以降低心血管风险的必要性。