Pivonello Rosario, Menafra Davide, Riccio Enrico, Garifalos Francesco, Mazzella Marco, de Angelis Cristina, Colao Annamaria
Dipartimento di Medicina Clinica e Chirurgia, Sezione di Endocrinologia, Centro di Andrologia, Medicina della Riproduzione e della Sessualità Maschile e Femminile (FERTISEXCARES), Università "Federico II" di Napoli, Naples, Italy.
Front Endocrinol (Lausanne). 2019 Jul 25;10:345. doi: 10.3389/fendo.2019.00345. eCollection 2019.
Several studies highlight that testosterone deficiency is associated with, and predicts, an increased risk of developing metabolic disorders, and, on the other hand, is highly prevalent in obesity, metabolic syndrome and type-2 diabetes mellitus. Models of gonadotropin releasing hormone deficiency, and androgen deprivation therapy in patients with prostate cancer, suggest that hypogonadotropic hypogonadism might contribute to the onset or worsening of metabolic conditions, by increasing visceral adiposity and insulin resistance. Nevertheless, in functional hypogonadism, as well as in late onset hypogonadism, the relationship between hypogonadotropic hypogonadism and metabolic disorders is bidirectional, and a vicious circle between the two components has been documented. The mechanisms underlying the crosstalk between testosterone deficiency and metabolic disorders include increased visceral adipose tissue and insulin resistance, leading to development of metabolic disorders, which in turn contribute to a further reduction of testosterone levels. The decrease in testosterone levels might be determined by insulin resistance-mediated and, possibly, pro-inflammatory cytokine-mediated decrease of sex hormone binding globulin, resulting in a temporary increased free testosterone available for aromatization to estradiol in visceral adipose tissue, followed by a subsequent decrease in free testosterone levels, due to the excess of visceral adipose tissue and aromatization; by a direct inhibitory effect of increased leptin levels on Leydig cells; and by a reduced gonadotropin secretion induced by estradiol, inflammatory mediators, leptin resistance, and insulin resistance, with the ultimate determination of a substantial hypogonadotropic hypogonadism. The majority of studies focusing on the effects of testosterone replacement therapy on metabolic profile reported a beneficial effect of testosterone on body weight, waist circumference, body mass index, body composition, cholesterol levels, and glycemic control. Consistently, several interventional studies demonstrated that correction of metabolic disorders, in particular with compounds displaying a greater impact on body weight and insulin resistance, improved testosterone levels. The aim of the current review is to provide a comprehensive overview on the relationship between hypogonadotropic hypogonadism and metabolism, by clarifying the independent role of testosterone deficiency in the pathogenesis of metabolic disorders, and by describing the relative role of testosterone deficiency and metabolic impairment, in the context of the bidirectional relationship between hypogonadism and metabolic diseases documented in functional hypogonadotropic hypogonadism. These aspects will be assessed by describing metabolic profile in men with hypogonadotropic hypogonadism, and androgenic status in men with metabolic disorders; afterwards, the reciprocal effects of testosterone replacement therapy and corrective interventions on metabolic derangements will be reported.
多项研究强调,睾酮缺乏与代谢紊乱风险增加相关且可预测该风险,另一方面,在肥胖、代谢综合征和2型糖尿病中睾酮缺乏极为普遍。促性腺激素释放激素缺乏模型以及前列腺癌患者的雄激素剥夺治疗表明,低促性腺激素性性腺功能减退可能通过增加内脏脂肪和胰岛素抵抗,促使代谢状况的发生或恶化。然而,在功能性性腺功能减退以及迟发性性腺功能减退中,低促性腺激素性性腺功能减退与代谢紊乱之间的关系是双向的,且二者之间的恶性循环已得到证实。睾酮缺乏与代谢紊乱之间相互作用的潜在机制包括内脏脂肪组织增加和胰岛素抵抗,进而导致代谢紊乱的发生,而这反过来又促使睾酮水平进一步降低。睾酮水平降低可能由胰岛素抵抗介导,也可能由促炎细胞因子介导的性激素结合球蛋白减少所致,从而导致可在内脏脂肪组织中芳香化为雌二醇的游离睾酮暂时增加,随后由于内脏脂肪组织过多和芳香化作用,游离睾酮水平又会降低;可能由瘦素水平升高对睾丸间质细胞的直接抑制作用导致;还可能由雌二醇、炎症介质、瘦素抵抗和胰岛素抵抗诱导的促性腺激素分泌减少导致,最终导致显著的低促性腺激素性性腺功能减退。大多数关注睾酮替代疗法对代谢状况影响的研究报告称,睾酮对体重、腰围、体重指数、身体成分、胆固醇水平和血糖控制具有有益作用。同样,多项干预性研究表明,纠正代谢紊乱,特别是使用对体重和胰岛素抵抗影响更大的化合物,可改善睾酮水平。本综述的目的是通过阐明睾酮缺乏在代谢紊乱发病机制中的独立作用,并描述在功能性低促性腺激素性性腺功能减退中记录的性腺功能减退与代谢疾病双向关系背景下睾酮缺乏和代谢损害的相对作用,全面概述低促性腺激素性性腺功能减退与代谢之间的关系。这些方面将通过描述低促性腺激素性性腺功能减退男性的代谢状况以及代谢紊乱男性的雄激素状态来评估;之后,将报告睾酮替代疗法和纠正干预对代谢紊乱的相互影响。