Sleep, carotid intima-media thickness, and arterial stiffness: results from a large longitudinal cohort study

动脉硬化 内膜中层厚度 队列 脉冲波速 心脏病学 医学 内科学 刚度 纵向研究 睡眠(系统调用) 颈动脉 计算机科学 血压 病理 工程类 结构工程 操作系统
作者
Ruirui Wang,Mengyao Shi,Xiangyan Yin,Yi Chen,Xiaoxiao Wang,Zhengbao Zhu,Tan Xu,Yonghong Zhang
出处
期刊:The Journals of Gerontology [Oxford University Press]
卷期号:80 (8)
标识
DOI:10.1093/gerona/glaf126
摘要

Abstract Background To evaluate the associations of sleep health with carotid intima-media thickness (CIMT) and arterial stiffness. Methods A total of 41 465 UK Biobank participants were included. Sleep traits were assessed at baseline via self-reported questionnaires, and a composite sleep score was constructed based on six factors: sleep duration, snoring, insomnia, chronotype, daytime napping, and daytime sleepiness, with higher scores indicating poorer sleep health. CIMT and arterial stiffness were measured at follow-up. Multivariable logistic regression was used to estimate odds ratios (ORs) and 95% confidence intervals (CIs) for the association between sleep score and study outcomes, adjusting for baseline demographics, socioeconomic status, physical measurements, and medication use. Results The mean age of the study population was 55.08 years (SD = 7.57), with 52.91% females and 96.99% Whites. Compared with those for participants with a sleep score of 0, the multivariate-adjusted ORs (95% CI) for those with sleep scores of 1, 2, 3, 4, and 5-6 were 1.04 (0.93, 1.16), 1.09 (0.98, 1.21), 1.17 (1.05, 1.30), 1.15 (1.02, 1.29), and 1.18 (1.03, 1.35) for CIMT thickening, respectively, and 1.04 (0.92, 1.18), 1.13 (1.00, 1.27), 1.25 (1.08, 1.40), 1.23 (1.08, 1.40), and 1.31 (1.12, 1.53) for arterial stiffness, respectively. Poor sleep health was associated with an increased risk of CIMT thickening within all genetic risk categories, and no interaction between the sleep and genetic risk scores was found. Conclusion This study highlighted the importance of healthy sleep behaviors in slowing the progression of subclinical cardiovascular disease, regardless of individual’s genetic risk status.
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