Division of Gastroenterology and Hepatology, University of California, San Francisco, San Francisco, California.
Division of Gastroenterology and Hepatology, Duke University, Durham, North Carolina.
Clin Gastroenterol Hepatol. 2021 Jun;19(6):1267-1274.e1. doi: 10.1016/j.cgh.2020.09.045. Epub 2020 Oct 1.
BACKGROUND & AIMS: Higher testosterone contributes to imaging-confirmed nonalcoholic fatty liver disease (NAFLD) in women, but whether testosterone influences their disease severity is unknown.
The association of free testosterone (free T) with nonalcoholic steatohepatitis (NASH) was determined in pre-menopausal women with biopsy-confirmed NAFLD (n = 207). Interaction testing was performed for age and free T given decline in testosterone with age, and association of aging with NASH. Regression models adjusted for abdominal adiposity, diabetes, and dyslipidemia.
Median age was 35 yrs (interquartile range, 29-41); 73% were white, 25% Hispanic; 32% had diabetes, 93% abdominal adiposity, and 95% dyslipidemia. 69% had NASH, 67% any fibrosis, and 15% advanced fibrosis. Higher free T levels were associated with NAFLD severity in younger women (interaction P value <.02). In the youngest age quartile, free T was independently associated with NASH (odds ratio [OR], 2.3; 95% CI, 1.2-4.4), NASH fibrosis (OR, 2.1; 95% CI, 1.1-3.8), and higher fibrosis stage (OR, 1.9; 95% CI, 1.1-3.4), P value .02. In these women, the proportion with NASH steadily rose from 27% to 88%, and with NASH fibrosis rose from 27% to 81%, with higher free T quartiles (P < .01). Free T was additionally associated with abdominal adiposity among all pre-menopausal women (OR, 2.2; 95% CI, 1.2-4.1: P = .02).
In young women with NAFLD, higher testosterone levels conferred a 2-fold higher risk of NASH and NASH fibrosis, and increased risk of abdominal adiposity, supporting a potential mechanistic link of abdominal fat on testosterone-associated liver injury. Testosterone may represent an early risk factor for NASH progression in young women, prior to their onset of more dominant, age-related metabolic risk factors.
较高的睾酮水平与女性经影像学证实的非酒精性脂肪性肝病(NAFLD)有关,但睾酮是否影响其疾病严重程度尚不清楚。
在经肝活检证实为 NAFLD 的绝经前女性(n=207)中,确定游离睾酮(free T)与非酒精性脂肪性肝炎(NASH)之间的关系。由于睾酮随年龄下降,因此进行了年龄与游离 T 的交互测试,以及衰老与 NASH 的关联分析。回归模型调整了腹部肥胖、糖尿病和血脂异常。
中位年龄为 35 岁(四分位距,29-41);73%为白人,25%为西班牙裔;32%患有糖尿病,93%存在腹部肥胖,95%存在血脂异常。69%患有 NASH,67%存在任何程度的纤维化,15%存在晚期纤维化。在年轻女性中,较高的游离 T 水平与 NAFLD 的严重程度相关(交互 P 值<.02)。在年龄最小的四分位数中,游离 T 与 NASH(比值比[OR],2.3;95%置信区间[CI],1.2-4.4)、NASH 纤维化(OR,2.1;95% CI,1.1-3.8)和较高的纤维化分期(OR,1.9;95% CI,1.1-3.4)独立相关,P 值<.02。在这些女性中,NASH 的比例从 27%稳步上升至 88%,NASH 纤维化的比例从 27%上升至 81%,游离 T 四分位数越高(P<.01)。游离 T 还与所有绝经前女性的腹部肥胖有关(OR,2.2;95% CI,1.2-4.1:P=.02)。
在患有 NAFLD 的年轻女性中,较高的睾酮水平使 NASH 和 NASH 纤维化的风险增加了 2 倍,并且使腹部肥胖的风险增加,这支持了腹部脂肪与睾酮相关肝损伤之间存在潜在的机制联系。在女性出现更为显著的年龄相关代谢危险因素之前,睾酮可能是年轻女性 NASH 进展的早期危险因素。