Altan Onat, Department of Cardiology, Cerrahpaşa Medical Faculty, Istanbul University, 34335 Etiler, Istanbul, Turkey.
World J Diabetes. 2013 Oct 15;4(5):219-25. doi: 10.4239/wjd.v4.i5.219.
To investigate whether serum adiponectin protects against cardiometabolic risk in a population sample with prevailing metabolic syndrome.
Middle-aged adults representative of a general population with baseline circulating adiponectin measurements (n = 1224) were analyzed prospectively at a mean of 3.8 years' follow-up, using continuous values or sex-specific tertiles. Total adiponectin was assayed by an ELISA kit. Type-2 diabetes was identified by criteria of the American Diabetes Association. Hypertension was defined as a blood pressure ≥ 140 mmHg and/or ≥ 90 mmHg and/or use of antihypertensive medication. Outcomes were predicted using Cox proportional hazards regression analysis in models that were controlled for potential confounders.
In models of multiple linear regression, sex hormone-binding globulin, fasting insulin (inverse) and, in men, age were significant independent covariates of serum adiponectin which further tended in women to be positively associated with serum creatinine. Cox regression analyses for incident coronary heart disease (CHD), adjusted for sex, age, non-HDL cholesterol, waist circumference and C-reactive protein, revealed significant inverse association with adiponectin tertiles in men but not women (HR = 0.66; 95%CI: 0.32-1.38 for highest tertile). Cox regression for type-2 diabetes in a similar model (wherein glucose replaced non-HDL cholesterol), adiponectin tertiles appeared to protect in each gender. HR for incident hypertension roughly displayed unity in each of the adiponectin tertiles (P-trend = 0.67).
High adiponectin levels failed to protect against the development of hypertension and, in women, against CHD, presumably paralleling impairment in renal function as well. Involvement of adiponectin in autoimmune complex with loss of antioxidative-antiatherogenic properties may be underlying.
探讨在代谢综合征流行的人群样本中,血清脂联素是否对心脏代谢风险具有保护作用。
对具有基线循环脂联素测量值的中年人群进行前瞻性分析(n=1224),这些人群代表了一般人群,随访平均时间为 3.8 年,使用连续值或性别特异性三分位数。使用 ELISA 试剂盒测定总脂联素。2 型糖尿病的诊断标准采用美国糖尿病协会的标准。高血压定义为血压≥140mmHg 和/或≥90mmHg 和/或使用降压药物。使用 Cox 比例风险回归分析模型,在控制潜在混杂因素的情况下预测结局。
在多元线性回归模型中,性激素结合球蛋白、空腹胰岛素(倒数)和男性的年龄是血清脂联素的显著独立协变量,进一步表明女性血清脂联素与血清肌酐呈正相关。调整性别、年龄、非高密度脂蛋白胆固醇、腰围和 C 反应蛋白后,Cox 回归分析显示,男性发生冠心病(CHD)的风险与脂联素三分位数呈显著负相关,但女性则无此相关性(HR=0.66;95%CI:0.32-1.38,最高三分位数)。在类似模型中(其中葡萄糖替代非高密度脂蛋白胆固醇),Cox 回归分析显示,脂联素三分位数在每个性别中都有保护作用。每个脂联素三分位的高血压发生率的 HR 大致为 1(P 趋势=0.67)。
高水平的脂联素不能预防高血压的发生,在女性中也不能预防 CHD,这可能与肾功能受损有关。脂联素可能与自身免疫复合物有关,导致其抗氧化-抗动脉粥样硬化的特性丧失。