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Steroid Sex Hormones, Sex Hormone–Binding Globulin, and Diabetes Incidence in the Diabetes Prevention Program.

机译:糖尿病预防计划中的类固醇激素,性激素结合球蛋白和糖尿病发病率。

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摘要

Context:: Steroid sex hormones and SHBG may modify metabolism and diabetes risk, with implications for sex-specific diabetes risk and effects of prevention interventions. Objective:: This study aimed to evaluate the relationships of steroid sex hormones, SHBG and SHBG single-nucleotide polymorphisms (SNPs) with diabetes risk factors and with progression to diabetes in the Diabetes Prevention Program (DPP). Design and Setting:: This was a secondary analysis of a multicenter randomized clinical trial involving 27 U.S. academic institutions. Participants:: The study included 2898 DPP participants: 969 men, 948 premenopausal women not taking exogenous sex hormones, 550 postmenopausal women not taking exogenous sex hormones, and 431 postmenopausal women taking exogenous sex hormones. Interventions:: Participants were randomized to receive intensive lifestyle intervention, metformin, or placebo. Main Outcomes:: Associations of steroid sex hormones, SHBG, and SHBG SNPs with glycemia and diabetes risk factors, and with incident diabetes over median 3.0 years (maximum, 5.0 y). Results:: T and DHT were inversely associated with fasting glucose in men, and estrone sulfate was directly associated with 2-hour post-challenge glucose in men and premenopausal women. SHBG was associated with fasting glucose in premenopausal women not taking exogenous sex hormones, and in postmenopausal women taking exogenous sex hormones, but not in the other groups. Diabetes incidence was directly associated with estrone and estradiol and inversely with T in men; the association with T was lost after adjustment for waist circumference. Sex steroids were not associated with diabetes outcomes in women. SHBG and SHBG SNPs did not predict incident diabetes in the DPP population. Conclusions:: Estrogens and T predicted diabetes risk in men but not in women. SHBG and its polymorphisms did not predict risk in men or women. Diabetes risk is more potently determined by obesity and glycemia than by sex hormones.
机译:背景:类固醇性激素和SHBG可能会改变新陈代谢和糖尿病风险,从而对特定性别的糖尿病风险和预防干预措施产生影响。目的::本研究旨在评估类固醇激素,SHBG和SHBG单核苷酸多态性(SNP)与糖尿病危险因素以及与糖尿病预防计划(DPP)的关系。设计与设置::这是对涉及27个美国学术机构的多中心随机临床试验的二次分析。参与者:该研究包括2898名DPP参与者:969名男性,948名未服用外源性激素的绝经前妇女,550名未服用外源性激素的绝经后妇女,以及431名未服用外源性激素的绝经后妇女。干预措施:参与者随机接受强化生活方式干预,二甲双胍或安慰剂。主要结果:类固醇性激素,SHBG和SHBG SNP与血糖和糖尿病危险因素以及中位3.0年(最大5.0岁)糖尿病的关联。结果:T和DHT与男性空腹血糖呈负相关,而硫酸雌酮与男性和绝经前女性2小时挑战后血糖直接相关。在未服用外源性激素的绝经前妇女和服用外源性激素的绝经后妇女中,SHBG与空腹血糖有关,而在其他人群中,SHBG与未服用外源性激素的妇女禁食葡萄糖有关。在男性中,糖尿病的发生与雌酮和雌二醇直接相关,而与T呈负相关。调整腰围后,与T的关联消失。性类固醇与妇女的糖尿病结局无关。 SHBG和SHBG SNP不能预测DPP人群中的糖尿病。结论:雌激素和T可预测男性而不是女性的糖尿病风险。 SHBG及其多态性不能预测男性或女性的风险。肥胖和血糖比由性激素更有效地决定糖尿病的风险。

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