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Disturbed Sleep as a Mechanism of Race Differences in Nocturnal Blood Pressure Non-Dipping.睡眠障碍是导致夜间血压非杓型节律种族差异的机制之一。
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J Clin Hypertens (Greenwich). 2019 Feb;21(2):184-192. doi: 10.1111/jch.13474. Epub 2019 Feb 5.
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CARDIA 研究中睡眠特征与夜间高血压和非杓型血压的关系。

Association of Sleep Characteristics With Nocturnal Hypertension and Nondipping Blood Pressure in the CARDIA Study.

机构信息

University of Alabama at Birmingham AL.

Columbia University New York NY.

出版信息

J Am Heart Assoc. 2020 Apr 7;9(7):e015062. doi: 10.1161/JAHA.119.015062. Epub 2020 Mar 19.

DOI:10.1161/JAHA.119.015062
PMID:32188307
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7428601/
Abstract

Background Sleep characteristics and disorders are associated with higher blood pressure (BP) when measured in the clinic setting. Methods and Results We tested whether self-reported sleep characteristics and likelihood of obstructive sleep apnea (OSA) were associated with nocturnal hypertension and nondipping systolic BP (SBP) among participants in the CARDIA (Coronary Artery Risk Development in Young Adults) study who completed 24-hour ambulatory BP monitoring during the year 30 examination. Likelihood of OSA was determined using the STOP-Bang questionnaire. Global sleep quality, habitual sleep duration, sleep efficiency, and midsleep time were obtained from the Pittsburgh Sleep Quality Index. Nocturnal hypertension was defined as mean asleep SBP ≥120 mm Hg or diastolic BP ≥70 mm Hg. Nondipping SBP was defined as a decline in awake-to-asleep SBP <10%. Among 702 participants, the prevalence of nocturnal hypertension and nondipping SBP was 41.3% and 32.5%, respectively. After multivariable adjustment including cardiovascular risk factors, the prevalence ratios (PRs) for nocturnal hypertension and nondipping SBP associated with high versus low likelihood of OSA were 1.32 (95% CI, 1.00-1.75) and 1.31 (95% CI, 1.02-1.68), respectively. The association between likelihood of OSA and nocturnal hypertension was stronger for white participants (PR: 2.09; 95% CI, 1.23-3.48) compared with black participants (PR: 1.11; 95% CI, 0.79-1.56). The PR for nondipping SBP associated with a 1-hour later midsleep time was 0.92 (95% CI, 0.85-0.99). Global sleep quality, habitual sleep duration, and sleep efficiency were not associated with either nocturnal hypertension or nondipping SBP. Conclusions These findings suggest that addressing OSA risk and sleep timing in a clinical trial may improve BP during sleep.

摘要

背景

在临床环境中测量时,睡眠特征和障碍与更高的血压(BP)有关。

方法和结果

我们测试了自我报告的睡眠特征和阻塞性睡眠呼吸暂停(OSA)的可能性是否与 CARDIA(年轻人冠状动脉风险发展)研究中的参与者在 30 岁检查期间完成的 24 小时动态血压监测期间的夜间高血压和非杓型收缩压(SBP)有关,该研究使用 STOP-Bang 问卷确定 OSA 的可能性。全球睡眠质量、习惯性睡眠时间、睡眠效率和午夜时间从匹兹堡睡眠质量指数中获得。夜间高血压定义为平均睡眠 SBP≥120mmHg 或舒张压≥70mmHg。非杓型 SBP 定义为觉醒至睡眠 SBP 下降<10%。在 702 名参与者中,夜间高血压和非杓型 SBP 的患病率分别为 41.3%和 32.5%。在包括心血管危险因素在内的多变量调整后,与 OSA 高可能性相关的夜间高血压和非杓型 SBP 的患病率比分别为 1.32(95%CI,1.00-1.75)和 1.31(95%CI,1.02-1.68)。与 OSA 可能性相关的夜间高血压与白人参与者的关联更强(PR:2.09;95%CI,1.23-3.48),而与黑人参与者的关联较弱(PR:1.11;95%CI,0.79-1.56)。午夜时间每延迟 1 小时,与非杓型 SBP 相关的 PR 为 0.92(95%CI,0.85-0.99)。全球睡眠质量、习惯性睡眠时间和睡眠效率与夜间高血压或非杓型 SBP 均无关。

结论

这些发现表明,在临床试验中解决 OSA 风险和睡眠时间可能会改善睡眠期间的 BP。