Department of Epidemiology and Public Health, University College London, London, UK.
Diabetes Care. 2012 Dec;35(12):2540-7. doi: 10.2337/dc11-2263. Epub 2012 Aug 28.
The role of adiponectin in the natural history of diabetes is not well characterized. We set out to characterize prediagnosis trajectories of adiponectin in individuals who develop type 2 diabetes.
In a case-cohort study (335 incident diabetes case and 2,474 noncase subjects) nested in the Whitehall II study, serum adiponectin was measured up to three times per participant (1991-1993, 1997-1999, and 2003-2004). Multilevel models adjusted for age and ethnicity were fitted to assess 13-year trajectories of log-transformed adiponectin preceding diabetes diagnosis or a randomly selected time point during follow-up (year(0)) based on 755/5,095 (case/noncase) person-examinations.
Adiponectin levels were lower in diabetes case than in noncase subjects (median 7,141 [interquartile range 5,187-10,304] vs. 8,818 [6,535-12,369] ng/mL at baseline, P < 0.0001). Control subjects showed a modest decline in adiponectin throughout follow-up (0.3% per year, P < 0.0001) at higher levels in women than in men (difference at year(0): 5,358 ng/mL, P < 0.0001). Female case and early-onset case (age at diagnosis <52 years) subjects had a steeper decline than control subjects (slope difference -1.1% per year, P = 0.001 in females, -1.6% per year in early-onset case subjects, P = 0.034). In men, adiponectin slopes for case and noncase subjects were parallel. The slope differences by diabetes onset were largely attenuated after adjustment for changes in obesity, whereas the sex-specific slope differences were independent of obesity.
Lower adiponectin levels were observed already a decade before the diagnosis of diabetes. The marked sex difference in trajectories suggests that sex-specific mechanisms affect the association between adiponectin levels and diabetes development.
脂联素在糖尿病自然史中的作用尚不清楚。本研究旨在描述发生 2 型糖尿病个体的脂联素在诊断前的轨迹。
在一项嵌套于 Whitehall II 研究的病例-队列研究中(335 例新发糖尿病病例和 2474 例非病例受试者),对每位参与者进行了多达 3 次血清脂联素测量(1991-1993 年、1997-1999 年和 2003-2004 年)。根据 755/5095 例(病例/非病例)个体检查,基于 13 年的随访时间(以年为单位),使用调整年龄和种族的多层次模型来评估糖尿病诊断前或随访期间任意时间点(年(0))的对数转换脂联素轨迹。
与非病例受试者相比,糖尿病病例的脂联素水平较低(中位数分别为 7141[四分位距 5187-10304]和 8818[6055-12369]ng/ml,P<0.0001)。在女性中,随着随访的进行,对照组的脂联素水平呈适度下降(每年 0.3%,P<0.0001),而在男性中则呈下降趋势(在年(0)时的差异:5358ng/ml,P<0.0001)。与对照组相比,女性病例和早发病例(诊断年龄<52 岁)的下降幅度更大(女性斜率差异为每年-1.1%,P=0.001,早发病例为每年-1.6%,P=0.034)。在男性中,病例和非病例的脂联素斜率相似。在调整肥胖变化后,糖尿病发病的斜率差异大部分减弱,而性别特异性斜率差异与肥胖无关。
在糖尿病诊断前 10 年就观察到了较低的脂联素水平。轨迹的显著性别差异表明,性别特异性机制影响脂联素水平与糖尿病发展之间的关联。