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Dysmetabolic syndrome in a man with a novel mutation of the aromatase gene: effects of testosterone, alendronate, and estradiol treatment

机译:患有芳香化酶基因新突变的男性的代谢异常综合征:睾丸激素,阿仑膦酸钠和雌二醇的治疗作用

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摘要

We present the fourth case of an adult man (29 yr old) affected by aromatase deficiency resulting from a novel homozygous inactivating mutation of the CYP19 ( P450(arom)) gene. At first observation, continuing linear growth, eunuchoid body proportions, diffuse bone pain, and bilateral cryptorchidism were observed. The patient presented also a complex dysmetabolic syndrome characterized by insulin resistance, diabetes mellitus type 2, acanthosis nigricans, liver steatohepatitis, and signs of precocious atherogenesis. The analysis of the effects induced by the successive treatment with high doses of testosterone, alendronate, and estradiol allows further insight into the roles of androgens and estrogens on several metabolic functions. High doses of testosterone treatment resulted in a severe imbalance in the estradiol to testosterone ratio together with the occurrence of insulin resistance and diabetes mellitus type 2. Estrogen treatment resulted in an improvement of acanthosis nigricans, insulin resistance, and liver steatohepatitis, coupled with a better glycemic control and the disappearance of two carotid plaques. Furthermore, the study confirms previous data concerning the key role of estrogens on male bone maturation, at least in part, and regulation of gonadotropin secretion. The biopsy of the testis showed a pattern of total germ cell depletion that might be due to the concomitant presence of bilateral cryptorchidism. Thus, a possible role of estrogen in male reproductive function is suggested but without revealing a direct cause-effect relationship. Data from this case provide new insights into the role of estrogens in glucose, lipid, and liver metabolism in men. This new case of aromatase deficiency confirms previous data on bone maturation and mineralization, and it reveals a high risk for the precocious development of cardiovascular disease in young aromatase-deficient men.
机译:我们介绍了第四例的成年男子(29岁),其受到由CYP19(P450(arom))基因的新型纯合失活突变导致的芳香化酶缺乏症的影响。初次观察时,观察到持续的线性生长,太监体比例,弥漫性骨痛和双侧隐睾症。该患者还出现了以胰岛素抵抗,2型糖尿病,黑棘皮病,肝脂肪性肝炎和性早熟动脉粥样硬化为特征的复杂的代谢异常综合征。对高剂量睾丸激素,阿仑膦酸和雌二醇连续治疗所诱发的作用进行分析,可以进一步了解雄激素和雌激素在几种代谢功能中的作用。高剂量的睾丸激素治疗会导致雌二醇与睾丸激素的比例严重失衡,同时还会出现胰岛素抵抗和2型糖尿病。雌激素治疗会改善黑棘皮症,胰岛素抵抗和肝脂肪性肝炎的改善,并改善病情。血糖控制和两个颈动脉斑块的消失。此外,该研究证实了以前有关雌激素在男性骨骼成熟中的关键作用(至少部分)和促性腺激素分泌调节的数据。睾丸活检显示出总生殖细胞消耗的模式,可能是由于双侧隐睾症的同时存在。因此,暗示了雌激素在男性生殖功能中的可能作用,但没有揭示直接的因果关系。该病例的数据提供了有关雌激素在男性葡萄糖,脂质和肝脏代谢中的作用的新见解。这例新的芳香酶缺乏症病例证实了先前有关骨骼成熟和矿化的数据,并且揭示了年轻的芳香酶缺乏症男性早熟发展心血管疾病的高风险。

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