Department of Experimental and Clinical Medicine, University Magna-Græcia of Catanzaro, Catanzaro, Italy.
Nutr Metab Cardiovasc Dis. 2011 Dec;21(12):933-40. doi: 10.1016/j.numecd.2010.02.008. Epub 2010 Aug 3.
Metabolically healthy but obese (MHO) subjects have a favourable cardio-metabolic risk profile, but whether they are also at lower risk for kidney dysfunction is still questionable.
A total of 106 MHO, 122 normal-weight and 212 insulin-resistant obese (IRO) subjects were stratified on the basis of their insulin sensitivity and body mass index (BMI). The CKD-EPI equation was used to estimate glomerular filtration rate (eGFR) and ISI index was used to estimate insulin sensitivity. eGFR was significantly lower in IRO as compared to MHO subjects after adjusting for age, gender and BMI (P = 0.008). In a logistic regression model adjusted for age, gender and BMI, IRO subjects showed an increased risk of having eGFR in the lowest quartile (odds ratio (OR) 1.91, 95% confidence interval (CI) 1.01-3.58; P = 0.04) as compared with MHO subjects. This association was maintained when waist, lean body mass, blood pressure, HDL cholesterol, triglyceride, fasting glucose and insulin levels were additionally included into the model (OR 2.49, 95%CI 1.17-5.27; P = 0.01), but its independence was not retained with further inclusion of insulin-like growth factor-1 (IGF-1) levels (OR 2.16, 95%CI 0.93-5.04; P = 0.07) No differences in eGFR were observed between non-obese and MHO individuals.
These results indicate that heterogeneity in obese phenotypes may account for conflicting evidence regarding the significance of obesity as a risk factor for chronic kidney disease. Our findings suggest that obesity is associated with lower kidney function only when insulin sensitivity is reduced, and that plasma IGF-1 is likely to be an important mechanism linking the IRO phenotype with reduced eGFR.
代谢健康但肥胖(MHO)人群具有有利的心血管代谢风险特征,但他们是否也具有较低的肾功能障碍风险仍存在疑问。
总共纳入了 106 名 MHO、122 名体重正常和 212 名胰岛素抵抗肥胖(IRO)患者,根据他们的胰岛素敏感性和体重指数(BMI)进行分层。采用 CKD-EPI 方程估计肾小球滤过率(eGFR),采用 ISI 指数估计胰岛素敏感性。调整年龄、性别和 BMI 后,IRO 组的 eGFR 明显低于 MHO 组(P=0.008)。在调整年龄、性别和 BMI 的逻辑回归模型中,IRO 组的 eGFR 处于最低四分位数的风险比(OR)为 1.91(95%置信区间(CI)为 1.01-3.58;P=0.04)高于 MHO 组。当将腰围、瘦体重、血压、高密度脂蛋白胆固醇、甘油三酯、空腹血糖和胰岛素水平纳入模型时,这种相关性仍然存在(OR 2.49,95%CI 1.17-5.27;P=0.01),但进一步纳入胰岛素样生长因子-1(IGF-1)水平后(OR 2.16,95%CI 0.93-5.04;P=0.07),其独立性不再保留。非肥胖者和 MHO 个体之间的 eGFR 没有差异。
这些结果表明,肥胖表型的异质性可能导致肥胖作为慢性肾脏病危险因素的重要性存在矛盾证据。我们的研究结果表明,只有当胰岛素敏感性降低时,肥胖才与肾功能下降相关,而血浆 IGF-1 可能是将 IRO 表型与降低的 eGFR 联系起来的重要机制。