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阻塞性睡眠呼吸暂停症状亚型和低氧负荷独立预测不同的心血管结局。

OSA symptom subtypes and hypoxic burden independently predict distinct cardiovascular outcomes.

作者信息

Mazzotti Diego R, Magalang Ulysses J, Keenan Brendan T, Mindel Jesse, Younes Magdy, Penzel Thomas, Pack Allan I, de Chazal Philip

机构信息

Division of Medical Informatics, Department of Internal Medicine, University of Kansas Medical Center, Kansas City, KS, USA.

Division of Pulmonary Critical Care and Sleep Medicine, Department of Internal Medicine, University of Kansas Medical Center, Kansas City, KS, USA.

出版信息

ERJ Open Res. 2025 Feb 25;11(1). doi: 10.1183/23120541.00511-2024. eCollection 2025 Jan.

Abstract

STUDY OBJECTIVES

Studies on obstructive sleep apnoea (OSA) have identified clinically relevant symptom-based subtypes and novel OSA-specific nocturnal hypoxic measures. Both traits are individually associated with cardiovascular outcomes, but evidence about their independent or shared effects is unknown. This study investigated the simultaneous contributions of OSA symptom subtypes and hypoxic burden (HB) on incident cardiovascular outcomes.

METHODS

Sleep Heart Health Study participants with high-quality oxygen saturation, apnoea-hypopnea index (AHI) and symptom data were included. Participants with OSA (AHI ≥5 events·h) were grouped into symptom subtypes. HB was calculated from respiratory event-related hypoxia. Cox proportional hazards models assessed whether symptom subtypes and/or HB were independently associated with cardiovascular mortality and major adverse cardiovascular events (MACE).

RESULTS

4396 participants free of cardiovascular disease were analysed, with median follow-up >11 years. Higher HB was associated with worse cardiovascular mortality (HR (95% CI): 1.63 (1.13-2.35); p=0.009) independently of symptom subtypes. Compared to those without OSA, the excessively sleepy OSA subtype had higher risk of incident MACE (1.62 (1.23-2.15); p<0.001), independently of HB. Among participants with moderate-severe OSA (AHI ≥15 events·h), excessively sleepy participants had higher risk of cardiovascular end-points compared to other subtypes, but HB was not associated with cardiovascular mortality or MACE risk.

CONCLUSION

OSA symptom subtypes and HB are independently associated with MACE and cardiovascular mortality, respectively. Thus, both are important for understanding OSA-related cardiovascular risk. Future studies using clinical samples including OSA therapy information that incorporate symptom subtypes and novel biomarkers, such as HB, could improve predictive models for cardiovascular disease risk.

摘要

研究目的

关于阻塞性睡眠呼吸暂停(OSA)的研究已经确定了基于临床相关症状的亚型以及新型的OSA特异性夜间低氧测量指标。这两个特征分别与心血管结局相关,但关于它们的独立或共同作用的证据尚不清楚。本研究调查了OSA症状亚型和低氧负担(HB)对心血管事件发生的同时影响。

方法

纳入睡眠心脏健康研究中具有高质量血氧饱和度、呼吸暂停低通气指数(AHI)和症状数据的参与者。OSA患者(AHI≥5次/小时)被分为症状亚型。HB由与呼吸事件相关的低氧情况计算得出。Cox比例风险模型评估症状亚型和/或HB是否与心血管死亡率和主要不良心血管事件(MACE)独立相关。

结果

对4396例无心血管疾病的参与者进行了分析,中位随访时间>11年。较高的HB与更差的心血管死亡率独立相关(HR(95%CI):1.63(1.13 - 2.35);p = 0.009),与症状亚型无关。与无OSA者相比,极度嗜睡的OSA亚型发生MACE的风险更高(1.62(1.23 - 2.15);p < 0.001),与HB无关。在中重度OSA患者(AHI≥15次/小时)中,极度嗜睡者与其他亚型相比发生心血管终点事件的风险更高,但HB与心血管死亡率或MACE风险无关。

结论

OSA症状亚型和HB分别与MACE和心血管死亡率独立相关。因此,两者对于理解OSA相关的心血管风险都很重要。未来使用包含OSA治疗信息、症状亚型和新型生物标志物(如HB)的临床样本进行的研究,可能会改进心血管疾病风险的预测模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f9d/11849095/96686e2deb9a/00511-2024.01.jpg

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