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合成代谢雄激素类固醇:一种可能的毒物相关脂肪性肝病新的危险因素。

Anabolic-androgenic steroids: a possible new risk factor of toxicant-associated fatty liver disease.

机构信息

Programa de Pós-Graduação em Medicina e Saúde (PPgMS), Faculdade de Medicina da Bahia, Universidade Federal da Bahia (UFBA), Salvador, Bahia, Brazil.

出版信息

Liver Int. 2011 Mar;31(3):348-53. doi: 10.1111/j.1478-3231.2010.02346.x. Epub 2010 Oct 11.

DOI:10.1111/j.1478-3231.2010.02346.x
PMID:21040407
Abstract

BACKGROUND

Industrial toxin and drugs have been associated with non-alcoholic fatty liver disease (NAFLD); in these cases, the disease has been termed toxicant-associated steatohepatitis (TASH).

AIM

This study hypothesizes that the use of anabolic-androgenic steroids (AAS) could also be a risk factor to TASH or better toxicant-associated fatty liver disease (TAFLD) development.

METHODOLOGY

Case-control study including 180 non-competitive recreational male bodybuilders from August/2007 to March/2009. Ninety-five had a history of intramuscular AAS use (cases; G1) and 85 were non-users (controls; G2). They underwent a clinical evaluation and abdominal ultrasound, and their blood levels of aminotransferases, creatine phosphokinase (CPK), lipids, glucose and insulin were measured. TAFLD criteria: history of AAS use >2 years; presence of hepatic steatosis on ultrasound and/or aminotransferase alterations with normal CPK levels; exclusion of ethanol intake ≥20 g/day or use of other drugs; and exclusion of obesity, dyslipidaemia, diabetes and other liver diseases. Homeostasis model assessment for insulin resistance ≥3 was considered insulin resistant. Independent t-test, odds ratio (OR) and 95% confidence intervals (95% CI) were calculated.

RESULTS

All cases were asymptomatic. Clinical and laboratorial data were similar in G1 and G2 (P>0.05). TAFLD criteria were observed in 12.6% of the G1 cases and 2.4% of controls had criteria compliant with non-alcoholic fatty liver related to metabolic conditions. OR was 6.0 (95% CI: 1.3-27.6).

CONCLUSIONS

These results suggest that AAS could be a possible new risk factor for TAFLD. In this type of fatty liver disease, the individuals had a low body fat mass and they did not present insulin resistance.

摘要

背景

工业毒素和药物与非酒精性脂肪性肝病(NAFLD)有关;在这些情况下,该疾病被称为毒物相关性脂肪性肝炎(TASH)。

目的

本研究假设使用合成代谢雄激素类固醇(AAS)也可能是 TASH 或更好的毒物相关性脂肪性肝病(TAFLD)发展的一个危险因素。

方法

包括 2007 年 8 月至 2009 年 3 月间 180 名非竞技性业余男性健美运动员的病例对照研究。95 名运动员有肌肉内 AAS 使用史(病例组;G1),85 名运动员为非使用者(对照组;G2)。他们接受了临床评估和腹部超声检查,并测量了他们的转氨酶、肌酸磷酸激酶(CPK)、血脂、血糖和胰岛素水平。TAFLD 标准:AAS 使用史>2 年;超声存在肝脂肪变性和/或转氨酶改变,CPK 水平正常;排除乙醇摄入量≥20 g/天或使用其他药物;排除肥胖、血脂异常、糖尿病和其他肝病。稳态模型评估的胰岛素抵抗指数≥3 被认为是胰岛素抵抗。计算了独立样本 t 检验、比值比(OR)和 95%置信区间(95%CI)。

结果

所有病例均无症状。G1 和 G2 之间的临床和实验室数据相似(P>0.05)。G1 组中有 12.6%的病例符合 TASH 标准,而对照组中有 2.4%的病例符合与代谢条件相关的非酒精性脂肪肝标准。OR 为 6.0(95%CI:1.3-27.6)。

结论

这些结果表明 AAS 可能是 TAFLD 的一个新的可能危险因素。在这种类型的脂肪肝疾病中,个体的体脂肪质量较低,且不存在胰岛素抵抗。

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