Albaaj F, Sivalingham M, Haynes P, McKinnon G, Foley R N, Waldek S, O'Donoghue D J, Kalra P A
Department of Renal Medicine, Hope Hospital, Salford, UK.
Postgrad Med J. 2006 Oct;82(972):693-6. doi: 10.1136/pgmj.2006.045963.
Hypogonadism in men may be secondary to renal failure and is well recognised in patients with end-stage renal disease. It is thought to contribute to the sexual dysfunction and osteoporosis experienced by these patients. However, the association between hypogonadism and lesser degrees of renal dysfunction is not well characterised.
The gonadal status of 214 male patients (mean age 56 (SD 18) years) attending a renal centre was studied; 62 of them were receiving haemodialysis and 22 continuous ambulatory peritoneal dialysis for end-stage renal disease, whereas 34 patients had functioning renal transplants and 96 patients were in the low-clearance phase. Non-fasting plasma was analysed for testosterone, follicle-stimulating hormone, luteinising hormone, sex hormone-binding globulin, parathyroid hormone and haemoglobin. Creatinine clearance was estimated in patients not on dialysis, and Kt/V and urea reduction ratio were assessed in patients on dialysis. Testosterone concentrations were classified as normal (>14 nmol/l), low-normal (10-14 nmol/l) or low (<10 nmol/l).
56 (26.2%) patients had significantly low testosterone levels and another 65 (30.3%) had low-normal levels. No significant changes were seen in sex hormone-binding globulin or gonadotrophin levels. Gonadal status was not correlated with haemoglobin level, parathyroid hormone level, creatinine clearance, or dialysis duration or adequacy.
Over half of patients with renal failure, even in the pre-dialysis phase, have low or low-normal levels of testosterone, which may be a potentially reversible risk factor for osteoporosis and sexual dysfunction. These patients may be candidates for testosterone-replacement therapy, which has been shown to improve bone mineral-density and libido in men with low and low-normal testosterone levels.
男性性腺功能减退可能继发于肾衰竭,在终末期肾病患者中已得到充分认识。人们认为它会导致这些患者出现性功能障碍和骨质疏松。然而,性腺功能减退与较轻程度肾功能不全之间的关联尚未得到充分描述。
对一家肾脏中心的214名男性患者(平均年龄56(标准差18)岁)的性腺状态进行了研究;其中62人因终末期肾病接受血液透析,22人接受持续性非卧床腹膜透析,34人有功能正常的肾移植,96人处于低清除率阶段。对非空腹血浆进行睾酮、促卵泡激素、促黄体激素、性激素结合球蛋白、甲状旁腺激素和血红蛋白分析。对未进行透析的患者估计肌酐清除率,对进行透析的患者评估Kt/V和尿素清除率。睾酮浓度分为正常(>14 nmol/l)、低正常(10 - 14 nmol/l)或低(<10 nmol/l)。
56名(26.2%)患者睾酮水平显著降低,另外65名(30.3%)患者睾酮水平低正常。性激素结合球蛋白或促性腺激素水平未见显著变化。性腺状态与血红蛋白水平、甲状旁腺激素水平、肌酐清除率、透析持续时间或充分性无关。
超过一半的肾衰竭患者,即使在透析前阶段,睾酮水平也处于低或低正常水平,这可能是骨质疏松和性功能障碍的一个潜在可逆危险因素。这些患者可能是睾酮替代治疗的候选者,睾酮替代治疗已被证明可改善睾酮水平低和低正常的男性的骨矿物质密度和性欲。