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男性体内性类固醇激素与肥胖对胰岛素抵抗及2型糖尿病的相互作用:第三次全国健康与营养检查调查

Interaction of sex steroid hormones and obesity on insulin resistance and type 2 diabetes in men: the Third National Health and Nutrition Examination Survey.

作者信息

Li Ji, Lai Hong, Chen Shaoguang, Zhu Hong, Lai Shenghan

机构信息

Department of Pathology, Johns Hopkins School of Medicine, Baltimore, MD, United States.

Department of Radiology, Johns Hopkins School of Medicine, Baltimore, MD, United States.

出版信息

J Diabetes Complications. 2017 Feb;31(2):318-327. doi: 10.1016/j.jdiacomp.2016.10.022. Epub 2016 Oct 22.

DOI:10.1016/j.jdiacomp.2016.10.022
PMID:27914732
Abstract

AIMS

We examined interaction of sex steroid hormones and obesity with regard to insulin resistance (IR) and type 2 diabetes (T2D) by using nationally representative data from the US.

METHODS

Data of 1461 men aged ≥20years who participated in the Third National Health and Nutrition Examination Survey were analyzed. Multiplicative interaction was calculated by cross-product interaction terms in multivariable logistic regression models. Additive interaction was assessed by the relative excess risk due to interaction (RERI).

RESULTS

After adjusting for demographic and lifestyle covariates, the odds of IR were greatest among obese men with low free testosterone and high androstanediol glucuronide. Multiplicative interactions for total testosterone, free testosterone, and free estradiol index (FEI) were statistically significant with central obesity but not with overweight and obesity regarding to T2D (P<0.05). Significant additive interactions with obesity or central obesity were detected for total testosterone (RERI=2.75, 95% CI=0.92,4.59), SHBG (RERI=5.71, 95% CI=0.77,10.64), and FEI (RERI=-9.96, 95% CI=-19.18,-0.74) with regard to IR, beta-cell dysfunction, and T2D.

CONCLUSIONS

Our findings add to the evidence suggesting that low testosterone and high estradiol may be associated greater risks of IR and T2D by interacting with overall and central obesity in adult men.

摘要

目的

我们利用来自美国的具有全国代表性的数据,研究了性类固醇激素与肥胖在胰岛素抵抗(IR)和2型糖尿病(T2D)方面的相互作用。

方法

对参加第三次全国健康和营养检查调查的1461名年龄≥20岁的男性的数据进行了分析。通过多变量逻辑回归模型中的交叉乘积交互项计算相乘交互作用。通过交互作用导致的相对超额风险(RERI)评估相加交互作用。

结果

在调整了人口统计学和生活方式协变量后,游离睾酮水平低、雄甾二醇葡萄糖醛酸苷水平高的肥胖男性发生IR的几率最高。总睾酮、游离睾酮和游离雌二醇指数(FEI)与中心性肥胖的相乘交互作用在统计学上具有显著性,但在T2D方面与超重和肥胖无关(P<0.05)。在IR、β细胞功能障碍和T2D方面,总睾酮(RERI=2.75,95%CI=0.92,4.59)、性激素结合球蛋白(SHBG)(RERI=5.71,95%CI=0.77,10.64)和FEI(RERI=-9.96,95%CI=-19.18,-0.74)与肥胖或中心性肥胖存在显著的相加交互作用。

结论

我们的研究结果进一步证明,低睾酮和高雌二醇可能通过与成年男性的全身肥胖和中心性肥胖相互作用,增加IR和T2D的风险。

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