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非肥胖非酒精性脂肪性肝病中非酒精性肝炎和显著纤维化的预测因素。

Predictors of nonalcoholic steatohepatitis and significant fibrosis in non-obese nonalcoholic fatty liver disease.

机构信息

Division of Gastroenterology and Hepatology, Stanford University School of Medicine, Stanford, California.

Division of Gastroenterology and Hepatology, Department of Internal Medicine, Seoul National University College of Medicine, Seoul Metropolitan Government Boramae Medical Center, Seoul, Korea.

出版信息

Liver Int. 2019 Feb;39(2):332-341. doi: 10.1111/liv.13983. Epub 2018 Oct 27.

Abstract

AIMS

We compared (a) demographic and clinical characteristics and (b) determinants of nonalcoholic steatohepatitis and significant fibrosis in non-obese and obese nonalcoholic fatty liver disease.

METHODS

A cross-sectional study of 664 Asian subjects (mean age 53.1 years; men 50.3%) with biopsy-proven nonalcoholic fatty liver disease and controls was conducted. Subjects were divided by their body mass index into obese (body mass index ≥25 kg/m ) and non-obese (body mass index <25 kg/m ).

RESULTS

Observations in subjects with non-obese nonalcoholic fatty liver disease were in between non-obese controls and subjects with obese nonalcoholic fatty liver disease for body mass index, sagittal abdominal diameter, aminotransferase levels, insulin resistance and abdominal visceral adipose tissue area. There was no significant difference in histology between non-obese and obese subjects with nonalcoholic fatty liver disease except for lower grade of hepatic steatosis in nonobese nonalcoholic fatty liver disease and higher severity of hepatic fibrosis in nonobese nonalcoholic steatohepatitis. Predictors of nonalcoholic steatohepatitis in nonobese subjects included females (odds ratio 2.49), higher alanine aminotransferase (odds ratio 1.03), lower high-density lipoprotein cholesterol (odds ratio 0.96), higher prevalence of diabetes (odds ratio 3.65) and higher visceral adipose tissue area (odds ratio 1.63 per standard deviation increase of visceral adipose tissue area) while age (odds ratio 1.04), higher aspartate aminotransferase (odds ratio 1.02), diabetes (odds ratio 2.76) and higher visceral adipose tissue area (odds ratio 1.57 per standard deviation increase) were associated with significant fibrosis in the non-obese. Sagittal abdominal diameter was independently associated with nonalcoholic steatohepatitis or significant fibrosis among subjects with non-obese nonalcoholic fatty liver disease.

CONCLUSION

While there were a few phenotypic differences from obese subjects, non-obese subjects with nonalcoholic fatty liver disease displayed a similar severity of histological liver damage. Potential factor(s) beyond obesity may play a role as non-obese nonalcoholic fatty liver disease advances to more severe disease.

摘要

目的

我们比较了(a)非肥胖和肥胖非酒精性脂肪性肝病患者的非酒精性肝炎和显著纤维化的人口统计学和临床特征,以及(b)这些特征的决定因素。

方法

对 664 名经肝活检证实的非酒精性脂肪性肝病患者和对照者进行了一项横断面研究(平均年龄 53.1 岁;男性占 50.3%)。根据体重指数(BMI)将患者分为肥胖组(BMI≥25kg/m²)和非肥胖组(BMI<25kg/m²)。

结果

非肥胖非酒精性脂肪性肝病患者的观察结果处于非肥胖对照组和肥胖非酒精性脂肪性肝病患者之间,BMI、矢状腹径、转氨酶水平、胰岛素抵抗和腹部内脏脂肪组织面积也是如此。非肥胖非酒精性脂肪性肝病患者与肥胖非酒精性脂肪性肝病患者之间的组织学无显著差异,除了非肥胖非酒精性脂肪性肝病患者肝脂肪变性程度较低,非肥胖非酒精性脂肪性肝炎患者肝纤维化程度较高。非肥胖患者发生非酒精性肝炎的预测因素包括女性(比值比 2.49)、较高的丙氨酸转氨酶(比值比 1.03)、较低的高密度脂蛋白胆固醇(比值比 0.96)、较高的糖尿病患病率(比值比 3.65)和较高的内脏脂肪组织面积(内脏脂肪组织面积每增加一个标准差的比值比为 1.63),而年龄(比值比 1.04)、较高的天门冬氨酸转氨酶(比值比 1.02)、糖尿病(比值比 2.76)和较高的内脏脂肪组织面积(内脏脂肪组织面积每增加一个标准差的比值比为 1.57)与非肥胖患者的显著纤维化相关。矢状腹径在非肥胖非酒精性脂肪性肝病患者中与非酒精性肝炎或显著纤维化独立相关。

结论

虽然与肥胖患者存在一些表型差异,但非肥胖非酒精性脂肪性肝病患者的组织学肝损伤严重程度相似。除肥胖以外的潜在因素可能在非肥胖非酒精性脂肪性肝病进展为更严重疾病时发挥作用。

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