Research Program in Men's Health: Aging and Metabolism, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Division of Radiology, Seattle Children's Hospital, Seattle, WA, USA.
Andrology. 2017 Sep;5(5):889-897. doi: 10.1111/andr.12392. Epub 2017 Jul 13.
Animal data shows that testosterone administration increases the volume of some parenchymal organs. However, the effects of exogenous testosterone on solid abdominal organs in humans remain unknown. The present study evaluated the effects of testosterone administration on the volume of liver, spleen and kidneys in a dose-response trial. Young healthy men aged 18-50 years participating in the 5α-Reductase (5aR) Trial. All participants received monthly injections of 7.5 mg leuprolide acetate to suppress endogenous testosterone secretion and weekly injections of 50, 125, 300 or 600 mg of testosterone enanthate, and were randomized to receive either 2.5 mg dutasteride (5 α-reductase inhibitor) or placebo daily for 20 weeks. Liver, spleen and kidney volumes were measured at baseline and the end of treatment using 1.5-Tesla magnetic resonance imaging. The dose-effect of testosterone on changes in the volume of parenchymal organs was evaluated by linear regression model. The association between changes in total testosterone (TT) levels and changes in organ volumes were assessed. Testosterone administration increased liver volume dose-dependently (17.4 cm per 100 mg of weekly testosterone enanthate; p = 0.031); the increase in liver volume was positively associated with changes in TT levels (R = 0.08, p = 0.024). A dose-dependent, but non-significant, increase in kidney volumes was also seen. Inclusion of dutasteride use into the models showed an independent association of randomization to dutasteride group with liver volume increase. In conclusion, Testosterone administration increased the liver volume in a dose-dependent manner. The potential changes in parenchymal organs should be considered when interpreting apparent changes in lean mass in response to anabolic interventions.
动物数据表明,睾丸酮的施用会增加一些实质器官的体积。然而,外源性睾丸酮对人体实质性腹部器官的影响尚不清楚。本研究在一项剂量反应试验中评估了睾丸酮给药对肝脏、脾脏和肾脏体积的影响。18-50 岁的年轻健康男性参加 5α-还原酶(5aR)试验。所有参与者每月接受 7.5 毫克亮丙瑞林醋酸酯注射,以抑制内源性睾丸酮分泌,每周接受 50、125、300 或 600 毫克庚酸睾丸酮注射,并随机接受 2.5 毫克度他雄胺(5α-还原酶抑制剂)或安慰剂,每天一次,共 20 周。在基线和治疗结束时使用 1.5-Tesla 磁共振成像测量肝脏、脾脏和肾脏的体积。通过线性回归模型评估睾丸酮对实质器官体积变化的剂量效应。评估总睾丸酮(TT)水平变化与器官体积变化之间的关系。睾丸酮给药剂量依赖性地增加肝脏体积(每周庚酸睾丸酮增加 100mg 时肝脏体积增加 17.4cm;p=0.031);肝脏体积的增加与 TT 水平的变化呈正相关(R=0.08,p=0.024)。也观察到肾脏体积的剂量依赖性但无显著性增加。将度他雄胺的使用纳入模型表明,随机分配到度他雄胺组与肝脏体积增加之间存在独立关联。总之,睾丸酮给药以剂量依赖性方式增加肝脏体积。在解释对合成代谢干预的瘦体重的明显变化时,应考虑实质器官的潜在变化。