首页> 外文期刊>Liver international : >Predictors of nonalcoholic steatohepatitis and significant fibrosis in non-obese nonalcoholic fatty liver disease
【24h】

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

机译:非酒精性脂肪性肝炎的预测因子,非酒精性脂肪肝疾病中的非酒精性脂肪性炎和显着纤维化

获取原文
获取原文并翻译 | 示例
           

摘要

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(2)) and non-obese (body mass index 25 kg/m(2)). 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.
机译:旨在比较(a)人口统计学和临床​​特征和(b)非酒精性脂肪磷脂炎和非酒精性脂肪肝疾病的显着纤维化的决定因素。方法对664名亚洲受试者(平均53.1岁的平均53.1岁;男性50.3%)进行活组织检查验证的非酒精性脂肪肝疾病和对照的横截面研究。将受试者除以肥胖的体重指数(体重指数& = 25kg / m(2))和非肥胖(体重指数&lt 2))。结果在非肥胖非酒精性脂肪肝疾病的受试者中的观察在非肥胖对照和受试者对体重指数,矢状腹直径,氨基转移酶水平,胰岛素抵抗和腹腔内膜脂肪组织区域之间的非酒精性脂肪肝疾病之间的观察。非酒精性脂肪肝病的非肥胖和肥胖受试者之间的组织学无显着差异,除了非酒精性脂肪肝病中的肝脏脂肪疾病的较低等级,肝纤维化肝脏肝硬化较高。非酒精脂肪肝炎的预测因子包括雌性(大量比率2.49),更高的丙氨酸氨基转移酶(大量比例1.03),较低的高密度脂蛋白胆固醇(差距为0.96),糖尿病患病率较高(差距3.65)和更高的内脏脂肪组织区域(可见脂肪组织面积的每个标准偏差增加的差距1.63),而年龄(差距1.04),较高的天冬氨酸氨基转移酶(差距1.02),糖尿病(差距2.76)和更高的内脏脂肪组织区域(每标准的赔率比1.57)偏差增加)与非肥胖的显着纤维化有关。矢状腹直径与非酒精性脂肪肝疾病的受试者的非酒精性脱脂性或显着纤维化有关。结论虽然肥胖受试者有几种表型差异,但非酒精性脂肪肝病的非肥胖受试者显示出类似的组织学肝损伤的严重程度。超越肥胖的潜在因素可能发挥非肥胖非酒精性脂肪肝病的作用,这是更严重的疾病。

著录项

  • 来源
    《Liver international :》 |2019年第2期|共10页
  • 作者单位

    Stanford Univ Sch Med Div Gastroenterol &

    Hepatol Stanford CA 94305 USA;

    Seoul Natl Univ Div Gastroenterol &

    Hepatol Dept Internal Med Coll Med Seoul Metropolitan Govt;

    Seoul Natl Univ Div Gastroenterol &

    Hepatol Dept Internal Med Coll Med Seoul Metropolitan Govt;

    Seoul Natl Univ Dept Pathol Coll Med Seoul Metropolitan Govt Boramae Med Ctr Seoul South Korea;

    Univ Oxford Radcliffe Dept Med Oxford England;

    Inova Fairfax Hosp Dept Med Ctr Liver Dis Falls Church VA USA;

    Stanford Univ Sch Med Div Gastroenterol &

    Hepatol Stanford CA 94305 USA;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 内科学;
  • 关键词

    body mass index; hepatic steatosis; lean;

    机译:体重指数;肝脏脂肪化;瘦;

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号