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基于英国生物库的前瞻性队列研究:加速度计测量的不规则睡眠持续时间与 2 型糖尿病风险的关联。

Association Between Accelerometer-Measured Irregular Sleep Duration and Type 2 Diabetes Risk: A Prospective Cohort Study in the UK Biobank.

机构信息

Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.

Division of Sleep and Circadian Disorders, Department of Medicine, Brigham and Women's Hospital, Boston, MA.

出版信息

Diabetes Care. 2024 Sep 1;47(9):1647-1655. doi: 10.2337/dc24-0213.

Abstract

OBJECTIVE

To evaluate the association between irregular sleep duration and incident diabetes in a U.K. population over 7 years of follow-up.

RESEARCH DESIGN AND METHODS

Among 84,421 UK Biobank participants (mean age 62 years) who were free of diabetes at the time of providing accelerometer data in 2013-2015 and prospectively followed until May 2022, sleep duration variability was quantified by the within-person SD of 7-night accelerometer-measured sleep duration. We used Cox proportional hazard models to estimate hazard ratios (HRs) for incident diabetes (identified from medical records, death register, and/or self-reported diagnosis) according to categories of sleep duration SD.

RESULTS

There were 2,058 incident diabetes cases over 622,080 person-years of follow-up. Compared with sleep duration SD ≤ 30 min, the HR (95% CI) was 1.15 (0.99, 1.33) for 31-45 min, 1.28 (1.10, 1.48) for 46-60 min, 1.54 (1.32, 1.80) for 61-90 min, and 1.59 (1.33, 1.90) for ≥91 min, after adjusting for age, sex, and race. We found a nonlinear relationship (P nonlinearity 0.0002), with individuals with a sleep duration SD of >60 vs. ≤60 min having 34% higher diabetes risk (95% CI 1.22, 1.47). Further adjustment for lifestyle, comorbidities, environmental factors, and adiposity attenuated the association (HR comparing sleep duration SD of >60 vs. ≤60 min: 1.11; 95% CI 1.01, 1.22). The association was stronger among individuals with lower diabetes polygenic risk score (PRS; P interaction ≤ 0.0264) and longer sleep duration (P interaction ≤ 0.0009).

CONCLUSIONS

Irregular sleep duration was associated with higher diabetes risk, particularly in individuals with a lower diabetes PRS and longer sleep duration.

摘要

目的

在一项为期 7 年的随访中,评估英国人群中不规则睡眠时长与新发糖尿病之间的关联。

研究设计与方法

在 2013-2015 年提供加速度计数据的 84421 名英国生物银行参与者(平均年龄 62 岁)中,[他们]在当时无糖尿病,且前瞻性随访至 2022 年 5 月,通过个体内 7 晚加速度计测量的睡眠时长的标准差来量化睡眠时长变异性。我们使用 Cox 比例风险模型,根据睡眠时长标准差的类别,估算新发糖尿病(通过医疗记录、死亡登记和/或自我报告的诊断确定)的风险比(HR)。

结果

在 622080 人年的随访中,共发生 2058 例新发糖尿病病例。与睡眠时长标准差≤30 分钟相比,31-45 分钟的 HR(95%CI)为 1.15(0.99,1.33),46-60 分钟为 1.28(1.10,1.48),61-90 分钟为 1.54(1.32,1.80),≥91 分钟为 1.59(1.33,1.90),校正年龄、性别和种族后。我们发现存在非线性关系(P 非线性性<0.0002),与睡眠时长标准差≤60 分钟的个体相比,睡眠时长标准差>60 分钟的个体发生糖尿病的风险高 34%(95%CI 1.22,1.47)。进一步调整生活方式、合并症、环境因素和肥胖情况,减弱了这种关联(与睡眠时长标准差>60 分钟相比,睡眠时长标准差≤60 分钟的 HR:1.11;95%CI 1.01,1.22)。在糖尿病多基因风险评分(PRS)较低(P 交互作用≤0.0264)和睡眠时长较长的个体中,这种关联更强(P 交互作用≤0.0009)。

结论

不规则睡眠时长与更高的糖尿病风险相关,尤其是在糖尿病 PRS 较低和睡眠时长较长的个体中。

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