National Institute of Allergy and Infectious Diseases, University of Maryland, Baltimore.
Critical Care Medicine Department, Clinical Center, National Institutes of Health, University of Maryland, Baltimore.
Clin Infect Dis. 2019 Aug 1;69(4):571-576. doi: 10.1093/cid/ciy965.
Hepatitis C virus (HCV) and hepatic dysfunction are associated with low total and free testosterone (TT and FT) and high sex hormone-binding globulin (SHBG). However, little is known about changes in testosterone following successful HCV treatment.
We evaluated testosterone levels and the prevalence of low testosterone in a cohort of 327 men with chronic HCV infection (human immunodeficiency virus [HIV] coinfection = 150) and in a subset of 85 men with testosterone levels obtained pre-HCV treatment and after sustained virologic response (SVR). Median follow-up was 36 months.
Participants with active HCV at baseline had higher TT (P < .0001) and SHBG (P < .0001) compared with participants who had achieved SVR, whereas FT did not differ. Low TT (<10.4 nmol/L) was more prevalent in participants with SVR compared with active HCV (P = .002); however, low FT (<0.1735 nmol/L) was common (50% active HCV, 43% SVR) and did not different between groups. For participants with longitudinal determinations, TT and SHBG decreased significantly (P < .0001) while FT remained unchanged post-SVR. Low FT persisted after SVR (pre-treatment 58%, post-SVR 54%, P = .72). HIV status and change in aspartate aminotrasferase-to-platelet ratio were significant independent predictors of change in FT following SVR.
During active HCV infection, testosterone deficiency may be masked due to elevated SHBG. Despite improvements in SHBG following SVR, low FT was common and persisted after HCV clearance, indicating the need for enhanced awareness and screening using estimates of FT following successful treatment of chronic HCV.
NCT01350648.
丙型肝炎病毒(HCV)和肝功能障碍与总睾酮(TT)和游离睾酮(FT)降低以及性激素结合球蛋白(SHBG)升高有关。然而,对于 HCV 治疗成功后睾酮的变化知之甚少。
我们评估了 327 名慢性 HCV 感染男性(人类免疫缺陷病毒 [HIV] 合并感染=150)队列和 85 名 HCV 治疗前和持续病毒学应答(SVR)后获得睾酮水平的亚组中睾酮水平和低睾酮的患病率。中位随访时间为 36 个月。
基线时患有活动性 HCV 的参与者 TT(P<0.0001)和 SHBG(P<0.0001)较高,而达到 SVR 的参与者 TT 较高(P<0.0001),而 FT 则没有差异。与 HCV 活跃的参与者相比,SVR 参与者中低 TT(<10.4 nmol/L)更为常见(SVR 为 0.002);然而,FT 较低(50%的 HCV 活跃,43%的 SVR)很常见,两组之间没有差异。对于具有纵向测定的参与者,TT 和 SHBG 在 SVR 后显著降低(P<0.0001),而 FT 则保持不变。SVR 后 FT 持续降低(治疗前为 58%,治疗后为 54%,P=0.72)。SVR 后 FT 变化的独立预测因素是 HIV 状态和天冬氨酸氨基转移酶-血小板比值的变化。
在 HCV 活跃感染期间,由于 SHBG 升高,可能会掩盖睾酮缺乏症。尽管 SVR 后 SHBG 有所改善,但 FT 仍很常见,并且在 HCV 清除后仍持续存在,这表明需要在慢性 HCV 成功治疗后使用 FT 估计值提高认识并进行筛查。
NCT01350648。