Obesity, Circulating Androgens and their Precursors

M. Dušková, H. Pospíšilová, M. Hill, Ľ. Stárka
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引用次数: 3

Abstract

Objective: The association of obesity with a lower circulating testosterone level in men is well documented. However, reports on possible changes in the androgen spectrum in obesity are rare. Methods: To investigate this phenomenon, serum sex hormone-binding globulin (SHBG), testosterone, dihydrotestosterone, androstenedione, dehydroepiandrosterone and its sulphate, 17α-hydroxypregnenolone, 17α-hydroxyprogesterone and gonadotrophins LH and FSH concentrations were measured in fasting blood samples of 224 men divided into three groups - normal (BMI=18-25, n=109, overweight (BMI 25.10-30, n=78) and obese (BMI=30.1-39, n=37). Results: A significant decrease in testosterone, dihydrotestosterone, 17α-hydroxypregnenolone, 17α-hydroxyprogesterone and SHBG with increasing body mass index was observed, whereas insignificant changes for dehydroepiandrosterone and its sulphate, androstenedione and gonadotrophins LH and FSH, were found. The ratios of corresponding pairs of steroids were in agreement with the concept that in obesity splitting of the side chain of C 21 -steroids, and 17β-hydroxysteroid dehydrogenase-reducing activity are decreased. No changes for steroid 5α-reductase or 3β-hydroxysteroid dehydrogenase (HSD3B2) were found. Conclusion: The findings demonstrate that, in men with increasing body mass index, the formation of C 19 steroids decreases from their C21 precursors and lower 17β-hydroxysteroid dehydrogenase further confines the production of testosterone and dihydrotestosterone.
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肥胖,循环雄激素及其前体
目的:肥胖与男性低循环睾酮水平的关系是有据可查的。然而,关于肥胖患者雄激素谱可能发生变化的报道很少。方法:将224名男性分为正常组(BMI=18 ~ 25, n=109)、超重组(BMI= 25.10 ~ 30, n=78)和肥胖组(BMI=30.1 ~ 39, n=37),测定其空腹血中性激素结合球蛋白(SHBG)、睾酮、二氢睾酮、雄烯二酮、脱氢表雄酮及其硫酸盐、17α-羟孕酮、17α-羟孕酮和促性腺激素LH、FSH浓度。结果:睾酮、二氢睾酮、17α-羟孕烯醇酮、17α-羟孕酮和SHBG随体重指数升高而显著降低,而脱氢表雄酮及其硫酸盐、雄烯二酮、促性腺激素LH和FSH变化不显著。相应的甾体对比值符合肥胖时c21 -甾体侧链分裂的概念,17β-羟基甾体脱氢酶还原活性降低。类固醇5α-还原酶和3β-羟基类固醇脱氢酶(HSD3B2)未见变化。结论:研究结果表明,在体重指数增加的男性中,c19类固醇的形成比C21前体减少,17β-羟基类固醇脱氢酶的降低进一步限制了睾酮和二氢睾酮的产生。
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