Gupta Kartik, Nagalli Shivaraj, Kalra Rajat, Gupta Rishab, Mahmood Shazil, Jain Vardhmaan, Zhou Wunan, Prabhu Sumanth D, Bajaj Navkaranbir S
Department of Internal Medicine, Henry Ford Hospital, Detroit, MI, U.S.A.
Division of Cardiovascular Disease and Comprehensive Cardiovascular Center, University of Alabama at Birmingham, AL, U.S.A.
Am J Prev Cardiol. 2021 Aug 17;8:100246. doi: 10.1016/j.ajpc.2021.100246. eCollection 2021 Dec.
The interplay between sleep duration and inflammation on the baseline and incident cardiovascular (CV) risk is unknown. We sought to evaluate the association between sleep duration, C-reactive protein (CRP), baseline CV risk, and incident CV mortality.
We used data from the National Health and Nutrition Examination Survey 2005-2010 linked with the cause of death data from the National Center for Health Statistics for adults aged ≥18 years. The associations between self-reported sleep duration and CRP, 10-year atherosclerotic CV disease risk score (ASCVD) and CV mortality were assessed using Linear, Poisson and Cox proportional hazard modeling as appropriate.
There were 17,635 eligible participants with a median age of 46 years (interquartile range [IQR] 31, 63). Among them, 51.3% were women and 46.9% were non-Hispanic Whites. Over a median follow-up of 7.5 years (IQR 6.0, 9.1), 350 CV deaths occurred at an incident rate of 2.7 per 1000-person years (IQR 2.4, 3.0). We observed a U-shaped associations between sleep duration and incident CV mortality rate (-trend=0.011), sleep duration and 10-year ASCVD risk (-trend <0.001), as well as sleep duration and CRP (-trend <0.001). A self-reported sleep duration of 6-7 hours appeared most optimal. We observed that those participants who reported <6 or >7 hours of sleep had higher risk of CV death attributable to inflammation after accounting for confounders.
There was a U-shaped relationship of incident CV mortality, 10-year ASCVD risk, and CRP with sleep duration. These findings suggest an interplay between sleep duration, inflammation, and CV risk.
睡眠时间与炎症在基线水平及心血管(CV)发病风险方面的相互作用尚不清楚。我们旨在评估睡眠时间、C反应蛋白(CRP)、基线CV风险和CV死亡发生率之间的关联。
我们使用了2005 - 2010年国家健康与营养检查调查的数据,并将其与国家卫生统计中心的成人(≥18岁)死亡原因数据相链接。根据情况,使用线性、泊松和Cox比例风险模型评估自我报告的睡眠时间与CRP、10年动脉粥样硬化性CV疾病风险评分(ASCVD)和CV死亡率之间的关联。
共有17635名符合条件的参与者,中位年龄为46岁(四分位间距[IQR]为31, 63)。其中,51.3%为女性,46.9%为非西班牙裔白人。在中位随访7.5年(IQR 6.0, 9.1)期间,发生了350例CV死亡,发生率为每1000人年2.7例(IQR 2.4, 3.0)。我们观察到睡眠时间与CV死亡发生率呈U型关联(-趋势=0.011),睡眠时间与10年ASCVD风险呈U型关联(-趋势<0.001),以及睡眠时间与CRP呈U型关联(-趋势<0.001)。自我报告的睡眠时间为6 - 7小时似乎最为理想。我们观察到,在考虑混杂因素后,那些报告睡眠时间<6小时或>7小时的参与者因炎症导致CV死亡的风险更高。
CV死亡发生率、10年ASCVD风险和CRP与睡眠时间呈U型关系。这些发现表明睡眠时间、炎症和CV风险之间存在相互作用。