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Sleep duration and incidence of type 2 diabetes: the Multiethnic Cohort

机译:睡眠时间和2型糖尿病的发病率:多种族队列

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ObjectivesAs an emerging risk factor for the rising incidence of type 2 diabetes, we examined sleep duration in relation to type 2 diabetes and several biomarkers.DesignProspective cohort recruited 1993-1996.SettingThe Multiethnic Cohort in Hawaii and California.ParticipantsA cohort of 151,691 White, African American, Japanese American, Native Hawaiian, and Latino participants; 9695 cohort members had biomarker measurements.MeasurementsSleep duration was self-reported at cohort entry. Diabetes status was obtained from 3 questionnaires and confirmed by 3 administrative data sources. Biomarkers were measured by standard assays 9.6±2.1 years after cohort entry. We estimated diabetes risk as a time-varying outcome using Cox regression adjusted for body mass index assessed at 3 time points and other known confounders and computed adjusted means of biomarkers by sleep hours.ResultsDuring 7.9±3.5 years of follow-up, 8487 new diabetes cases were diagnosed. Long sleep duration (≥9 hours), as compared with 7-8 hours, was significantly associated with higher incidence (hazard ratio, 1.12; 95% confidence interval 1.04-1.21), but the 4% elevated incidence for short sleep duration (≤6 hours) did not reach significance (95% confidence interval 0.99-1.09). After stratification, the associations appeared stronger in Japanese American than other ethnic groups and in participants without comorbidity. Hours of sleep were positively associated with C-reactive protein and triglycerides and inversely related to high-density lipoprotein cholesterol and adiponectin but not with leptin levels and homeostatic model assessment of insulin resistance.ConclusionIn this multiethnic population, the 12% higher diabetes risk for long sleep hours may be mediated through inflammation, a poor lipid profile, and lower adiponectin levels.
机译:目标是2型糖尿病发病率上升的新出现的危险因素,我们研究了与2型糖尿病和几种生物标志物相关的睡眠持续时间.DesignProSpeive Cohort 1993-1996。在夏威夷和加利福尼亚州的不同种族队列.Parcipantsa队列151,691白人,非洲人美国,日本美国,夏威夷和拉丁裔参与者; 9695群组成员患有生物标志物测量。索赔持续时间在群组中自我报告。糖尿病状态是从3问卷获得的,并通过3个行政数据来源确认。在队列进入后,通过标准测定法测量生物标志物9.6±2.1岁。我们估计糖尿病风险作为使用COX回归的时变的结果,用于在3个时间点和其他已知的混淆和其他已知的混血仪中评估的体重指数,并通过睡眠时间计算调整后的生物标志物手段。方法对7.9±3.5岁的后续行动,8487名新糖尿病病例被诊断出来。长期睡眠持续时间(≥9小时)与7-8小时相比,与较高的发病率(危险比为1.12; 95%置信区间1.04-1.21)显着相关,但短睡眠持续时间的4%升高(≤ 6小时)没有意义(95%置信区间0.99-1.09)。分层后,联合会在日本美国比其他族裔和参与者在没有合并症的情况下出现更强大。睡眠时间与C反应性蛋白质和甘油三酯呈正相关,与高密度脂蛋白胆固醇和脂联素相反,但没有瘦素水平和稳态模型评估胰岛素抵抗。结论这种多民族人群,长期以来12%的糖尿病风险增加12%的糖尿病风险睡眠时间可能通过炎症,脂肪曲线和降低脂联素水平介导。

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