Cundy T, Bomford A, Butler J, Wheeler M, Williams R
Department of Medicine, King's College Hospital, London, United Kingdom.
J Clin Endocrinol Metab. 1989 Jul;69(1):110-6. doi: 10.1210/jcem-69-1-110.
The contribution of diabetes and cirrhosis to sexual dysfunction and hypogonadism was evaluated by two-way analysis of variance in a group of 30 men with idiopathic hemochromatosis. The prevalence of severe sexual dysfunction was significantly higher in men with hemochromatosis than in a control group matched for prevalence of diabetes and age (P less than 0.001). In both controls and hemochromatosis patients the presence of diabetes was significantly associated with sexual dysfunction (P less than 0.005), but the more severe symptoms in the hemochromatosis patients were related to the additive effects of hypoandrogenism (P less than 0.01). Sexual dysfunction was a common early complaint in hemochromatosis patients, but these symptoms were frequently overlooked, leading to diagnostic delay. Mean testicular volume was a useful measure of gonadal status, being significantly correlated with indices of serum free testosterone (rs = 0.83; P less than 0.01) and LH (rs = 0.71; P less than 0.001). The presence of cirrhosis did not contribute significantly to symptomatology, but had an effect independent of and additive to hypogonadotropic hypogonadism in reducing serum free testosterone (P less than 0.02) and estradiol (P less than 0.002), an effect apparently mediated through central rather than testicular mechanisms. Hypoandrogenism was associated with an increase in serum sex hormone-binding globulin (SHBG) concentrations (P less than 0.005), but cirrhosis also had an independent effect in raising SHBG (P less than 0.005), which could not be accounted for by changes in circulating sex hormone concentrations. Thus, the evaluation of sexual dysfunction or hypogonadism in men with hemochromatosis requires consideration of the effects of both diabetes and cirrhosis. Because of the greater variance in SHBG some estimate of free testosterone rather than total testosterone is preferable.
通过双向方差分析,对一组30名特发性血色素沉着症男性患者评估了糖尿病和肝硬化对性功能障碍和性腺功能减退的影响。血色素沉着症男性患者中重度性功能障碍的患病率显著高于糖尿病患病率和年龄相匹配的对照组(P<0.001)。在对照组和血色素沉着症患者中,糖尿病的存在均与性功能障碍显著相关(P<0.005),但血色素沉着症患者更严重的症状与雄激素缺乏的叠加效应有关(P<0.01)。性功能障碍是血色素沉着症患者常见的早期主诉,但这些症状常被忽视,导致诊断延迟。平均睾丸体积是性腺状态的有用指标,与血清游离睾酮指数(rs = 0.83;P<0.01)和促黄体生成素(rs = 0.71;P<0.001)显著相关。肝硬化的存在对症状学的影响不显著,但在降低血清游离睾酮(P<0.02)和雌二醇(P<0.002)方面,具有独立于促性腺激素缺乏性性腺功能减退且与之相加的作用,这种作用显然是通过中枢而非睾丸机制介导的。雄激素缺乏与血清性激素结合球蛋白(SHBG)浓度升高相关(P<0.005),但肝硬化在升高SHBG方面也有独立作用(P<0.005),这不能用循环性激素浓度的变化来解释。因此,评估血色素沉着症男性患者的性功能障碍或性腺功能减退需要考虑糖尿病和肝硬化两者的影响。由于SHBG的变异性更大,最好评估游离睾酮而非总睾酮。