Department of Clinical Sciences, Lund University, Skåne University Hospital, CRC, Jan Waldenströms gata 35, 20502, Malmö, Sweden.
Department of Diabetes and Metabolic Diseases, University of Tokyo, Tokyo, Japan.
Diabetologia. 2018 Feb;61(2):331-341. doi: 10.1007/s00125-017-4464-3. Epub 2017 Nov 4.
AIMS/HYPOTHESIS: Sleep duration is a risk factor for incident diabetes mellitus and CHD. The primary aim of the present study was to investigate, in sex-specific analyses, the role of incident diabetes as the possible biological mechanism for the reported association between short/long sleep duration and incident CHD. Considering that diabetes is a major risk factor for CHD, we hypothesised that any association with sleep duration would not hold for cases of incident CHD occurring before incident diabetes ('non-diabetes CHD') but would hold true for cases of incident CHD following incident diabetes ('diabetes-CHD').
A total of 6966 men and 9378 women aged 45-73 years from the Malmö Diet Cancer Study, a population-based, prospective cohort, who had answered questions on habitual sleep duration and did not have a history of prevalent diabetes or CHD were included in the analyses. Incident cases of diabetes and CHD were identified using national registers. Sex-specific Cox proportional hazards regression models were stratified by BMI and adjusted for known covariates of diabetes and CHD.
Mean follow-up times for incident diabetes (n = 1137/1016 [men/women]), incident CHD (n = 1170/578), non-diabetes CHD (n = 1016/501) and diabetes-CHD (n = 154/77) were 14.2-15.2 years for men, and 15.8-16.5 years for women. In men, short sleep duration (< 6 h) was associated with incident diabetes (HR 1.35, 95% CI 1.01, 1.80), CHD (HR 1.41, 95% CI 1.06, 1.89) and diabetes-CHD (HR 2.34, 95% CI 1.20, 4.55). Short sleep duration was not associated with incident non-diabetes CHD (HR 1.35, 95% CI 0.98, 1.87). Long sleep duration (≥ 9 h) was associated with incident diabetes (HR 1.37, 95% CI 1.03, 1.83), CHD (HR 1.33, 95% CI 1.01, 1.75) and diabetes-CHD (HR 2.10, 95% CI 1.11, 4.00). Long sleep duration was not associated with incident non-diabetes CHD (HR 1.33, 95% CI 0.98, 1.80). In women, short sleep duration was associated with incident diabetes (HR 1.53, 95% CI 1.16, 2.01), CHD (HR 1.46, 95% CI 1.03, 2.07) and diabetes-CHD (HR 2.88, 95% CI 1.37, 6.08). Short sleep duration was not associated with incident non-diabetes CHD (HR 1.29, 95% CI 0.86, 1.93).
CONCLUSIONS/INTERPRETATION: The associations between sleep duration and incident CHD directly reflect the associations between sleep duration and incident diabetes. Incident diabetes may thus be the explanatory mechanism for the association between short and long sleep duration and incident CHD.
目的/假设:睡眠时长是发生糖尿病和冠心病的一个风险因素。本研究的主要目的是在性别特异性分析中,探究新发糖尿病是否可能是睡眠时长与新发冠心病之间关联的生物学机制。鉴于糖尿病是冠心病的一个主要危险因素,我们假设,对于新发冠心病病例(非糖尿病性冠心病),与睡眠时长相关的任何关联都不成立,而对于新发糖尿病后发生的新发冠心病病例(糖尿病性冠心病),这种关联则成立。
本研究纳入了年龄在 45-73 岁之间的来自马尔默饮食癌症研究的 6966 名男性和 9378 名女性,这是一个基于人群的前瞻性队列,他们回答了关于习惯性睡眠时长的问题,且没有糖尿病或冠心病的既往病史。通过国家登记册确定新发糖尿病和冠心病的病例。性别特异性 Cox 比例风险回归模型根据 BMI 进行分层,并对糖尿病和冠心病的已知协变量进行了调整。
新发糖尿病(n=1137/1016[男性/女性])、新发冠心病(n=1170/578)、非糖尿病性冠心病(n=1016/501)和糖尿病性冠心病(n=154/77)的平均随访时间,男性为 14.2-15.2 年,女性为 15.8-16.5 年。在男性中,短睡眠时间(<6 小时)与新发糖尿病(HR 1.35,95%CI 1.01,1.80)、冠心病(HR 1.41,95%CI 1.06,1.89)和糖尿病性冠心病(HR 2.34,95%CI 1.20,4.55)相关。短睡眠时间与非糖尿病性冠心病(HR 1.35,95%CI 0.98,1.87)无关。长睡眠时间(≥9 小时)与新发糖尿病(HR 1.37,95%CI 1.03,1.83)、冠心病(HR 1.33,95%CI 1.01,1.75)和糖尿病性冠心病(HR 2.10,95%CI 1.11,4.00)相关。长睡眠时间与非糖尿病性冠心病(HR 1.33,95%CI 0.98,1.80)无关。在女性中,短睡眠时间与新发糖尿病(HR 1.53,95%CI 1.16,2.01)、冠心病(HR 1.46,95%CI 1.03,2.07)和糖尿病性冠心病(HR 2.88,95%CI 1.37,6.08)相关。短睡眠时间与非糖尿病性冠心病(HR 1.29,95%CI 0.86,1.93)无关。
结论/解释:睡眠时长与新发冠心病之间的关联直接反映了睡眠时长与新发糖尿病之间的关联。因此,新发糖尿病可能是睡眠时长与新发冠心病之间关联的解释机制。