Department of Epidemiology and Public Health, University College London, London, UK.
Obesity (Silver Spring). 2012 Jan;20(1):229-32. doi: 10.1038/oby.2011.209. Epub 2011 Jul 21.
An emerging body of evidence suggests that sedentary behavior (SB) is an independent risk factor for cardiometabolic disease. Recent data suggest that multi-domain SB has detrimental associations with BMI, waist circumference (WC), and nonadiposity-related (total cholesterol, high density lipoprotein cholesterol (HDL-C), systolic (SBP) and diastolic (DBP) blood pressure) cardiometabolic risk markers. The aim of this cross-sectional study was to examine the extent to which the associations between SB and nonadiposity-related cardiometabolic risk markers are explained by adiposity markers. Subjects were 5,067 Health Survey for England (HSE) 2008 respondents (2,552 men) aged 16-65 years. The measurements protocol involved self-reports of television time, other recreational sitting, occupational sitting/standing, physical activity and objective measures of weight, height, WC, total cholesterol, HDL cholesterol, SBP, and DBP. BMI or WC adjustments of the multivariable models looking at the associations between SB and nonadiposity markers attenuated all associations towards the null. Using established logistic regression-based algorithms we calculated that a large percentage of the associations between SB time and nonadiposity risk factors is explained by BMI or WC (range: 27.3-95.9%). Future longitudinal studies should further examine the mediatory role of adiposity in explaining the associations between SB and cardiometabolic risk.
越来越多的证据表明,久坐行为(SB)是心血管代谢疾病的一个独立危险因素。最近的数据表明,多领域 SB 与 BMI、腰围(WC)和非肥胖相关(总胆固醇、高密度脂蛋白胆固醇(HDL-C)、收缩压(SBP)和舒张压(DBP)血压)心血管代谢风险标志物有不利关联。本横断面研究旨在探讨 SB 与非肥胖相关心血管代谢风险标志物之间的关联在多大程度上可以用肥胖标志物来解释。研究对象为英格兰健康调查(HSE)2008 年的 5067 名受访者(2552 名男性),年龄在 16-65 岁之间。测量方案包括电视时间、其他娱乐性坐姿、职业坐姿/站立、体力活动以及体重、身高、WC、总胆固醇、HDL 胆固醇、SBP 和 DBP 的客观测量。在多变量模型中对 SB 和非肥胖标志物之间的关联进行 BMI 或 WC 调整后,所有关联均向零值减弱。我们使用既定的基于逻辑回归的算法计算出,SB 时间与非肥胖危险因素之间的关联有很大一部分可以用 BMI 或 WC 来解释(范围:27.3%-95.9%)。未来的纵向研究应进一步研究肥胖在解释 SB 与心血管代谢风险之间关联中的中介作用。