Ley Sylvia H, Harris Stewart B, Connelly Philip W, Mamakeesick Mary, Gittelsohn Joel, Hegele Robert A, Retnakaran Ravi, Zinman Bernard, Hanley Anthony J G
Department of Nutritional Sciences, University of Toronto, Toronto, Ontario, Canada.
Diabetes Care. 2008 Jul;31(7):1410-5. doi: 10.2337/dc08-0036. Epub 2008 Mar 13.
The aim of this study was to investigate associations of adiponectin, leptin, C-reactive protein (CRP), interleukin (IL)-6, and serum amyloid A (SAA), individually or in combinations, with risk of incident type 2 diabetes in a Aboriginal Canadian [corrected] population.
Of the 606 Sandy Lake Health and Diabetes Project cohort subjects who were free of diabetes at baseline, 540 (89.1%) participated in 10-year follow-up assessments. Concentrations of fasting adiponectin, leptin, CRP, IL-6, SAA, and covariates were measured at baseline. Fasting glucose and a 75-g oral glucose tolerance test were obtained at baseline and follow-up to determine incident type 2 diabetes, defined as clinically diagnosed type 2 diabetes or as fasting plasma glucose > or =7.0 mmol/l or 2-h postload plasma glucose > or =11.1 mmol/l at follow-up.
Low adiponectin, high leptin, and low adiponectin-to-leptin ratio at baseline were associated with increased risk of incident type 2 diabetes after adjustment for age, sex, triglycerides, HDL cholesterol, hypertension, and impaired glucose tolerance (odds ratio 0.63 [95% CI 0.48-0.83], 1.50 [1.02-2.21], and 0.54 [0.37-0.77], respectively). When the models were additionally adjusted for waist circumference or BMI, however, only low adiponectin remained significantly associated with increased incident diabetes (0.68 [0.51-0.90]). Combinations of leptin, CRP, IL-6, and/or SAA with adiponectin, assessed using either the ratio or joint effects, did not improve diabetes prediction.
Low baseline adiponectin is associated with increased risk of incident type 2 diabetes independent of leptin, CRP, IL-6, SAA, and metabolic syndrome variables including obesity.
本研究旨在调查脂联素、瘦素、C反应蛋白(CRP)、白细胞介素(IL)-6和血清淀粉样蛋白A(SAA)单独或联合与加拿大原住民人群2型糖尿病发病风险的关联。
在桑迪湖健康与糖尿病项目队列的606名基线时无糖尿病的受试者中,540名(89.1%)参与了为期10年的随访评估。在基线时测量空腹脂联素、瘦素、CRP、IL-6、SAA的浓度以及协变量。在基线和随访时进行空腹血糖和75克口服葡萄糖耐量试验,以确定2型糖尿病发病情况,2型糖尿病定义为临床诊断的2型糖尿病或随访时空腹血糖≥7.0 mmol/l或负荷后2小时血糖≥11.1 mmol/l。
在调整年龄、性别、甘油三酯、高密度脂蛋白胆固醇、高血压和糖耐量受损后,基线时低脂联素、高瘦素和低脂联素与瘦素比值与2型糖尿病发病风险增加相关(比值比分别为0.63 [95%可信区间0.48 - 0.83]、1.50 [1.02 - 2.21]和0.54 [0.37 - 0.77])。然而,当模型进一步调整腰围或体重指数时,只有低脂联素仍与糖尿病发病风险增加显著相关(0.68 [0.51 - 0.90])。使用比值或联合效应评估的瘦素、CRP、IL-6和/或SAA与脂联素的组合并未改善糖尿病预测。
基线低脂联素与2型糖尿病发病风险增加相关,独立于瘦素、CRP、IL-6、SAA以及包括肥胖在内的代谢综合征变量。