Urology Institute, University Hospitals, Case Western Reserve University School of Medicine, Cleveland, OH, USA.
Translational Biology and Molecular Medicine, Scott Department of Urology, Baylor College of Medicine, Houston, TX, USA.
Int J Impot Res. 2022 Jan;34(1):50-54. doi: 10.1038/s41443-020-00361-z. Epub 2020 Oct 7.
Male solid organ transplant patients are at increased risk of hypogonadism and the safety of treating these patients for hypogonadism is unknown. We sought to evaluate the safety of treating hypogonadism in the solid organ transplant recipient. To accomplish this, we performed a retrospective review between 2009 and 2017 of patients treated at a single academic urology clinic. Men who underwent a solid organ transplant with a diagnosis of hypogonadism (Testosterone <350 ng/dl) were included. In total, 87 hypogonadal transplant recipients were included (29 no treatment; 58 treated). Treatment modalities included non-testosterone therapies (human chorionic gonadotropin, clomiphene), topical, injectable, and subcutaneous T preparations. There was no difference between groups for baseline characteristics including age, length of follow-up since transplant, baseline testosterone, and transplant type. There was no difference in prostate cancer diagnoses, erythrocytosis, rejection, infections, number of unplanned admissions per patient. While there was no difference in the proportion of deaths in untreated (21%; n = 6) and treated transplant recipients (7%; n = 4; p = 0.08), the median survival was longer in men treated with T (p = 0.03). Treatment of hypogonadism in solid organ recipients did not increase the risk for adverse effects related to treatment of hypogonadism or solid organ transplant.
男性实体器官移植患者患性腺功能减退症的风险增加,而治疗这些患者性腺功能减退症的安全性尚不清楚。我们旨在评估治疗实体器官移植受者性腺功能减退症的安全性。为了实现这一目标,我们对 2009 年至 2017 年在一家学术泌尿科诊所接受治疗的患者进行了回顾性研究。患有性腺功能减退症(睾酮<350ng/dl)并接受过实体器官移植的男性被纳入研究。共有 87 名性腺功能减退的移植受者(29 名未接受治疗;58 名接受治疗)。治疗方法包括非睾酮疗法(人绒毛膜促性腺激素、氯米芬)、局部、注射和皮下 T 制剂。两组在基线特征方面没有差异,包括年龄、移植后随访时间、基线睾酮和移植类型。前列腺癌诊断、红细胞增多症、排斥反应、感染、每位患者的非计划入院次数均无差异。未治疗(21%;n=6)和治疗的移植受者(7%;n=4;p=0.08)之间的死亡率无差异,但接受 T 治疗的男性中位生存期更长(p=0.03)。治疗实体器官受者的性腺功能减退症并不会增加与治疗性腺功能减退症或实体器官移植相关的不良反应风险。