کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
3264373 1207785 2011 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
High liver RBP4 protein content is associated with histological features in patients with genotype 1 chronic hepatitis C and with nonalcoholic steatohepatitis
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی غدد درون ریز، دیابت و متابولیسم
پیش نمایش صفحه اول مقاله
High liver RBP4 protein content is associated with histological features in patients with genotype 1 chronic hepatitis C and with nonalcoholic steatohepatitis
چکیده انگلیسی

Background and aimTo investigate the hepatic expression of retinol-binding protein-4 (RBP4) in chronic hepatitis C (CHC) and nonalcoholic steatohepatitis (NASH) patients, and its association with biochemical and histological patterns of liver damage.Materials and methodsSixty-six genotype 1 CHC and 32 NASH patients were tested for hepatic RBP4 expression. Liver expression at immunostaining was scored as 0 (slight), 1 (mild), 2 (moderate), and 3 (intense). In addition, the mRNA and the quantitative protein expressions of RBP4 were tested by PCR and by western blot, respectively, in 12 NASH and 28 CHC patients. Twelve subjects undergoing elective cholecystectomy served as controls.ResultsTen (31%), 16 (50%) and 6 (19%) NASH patients, and 21 (32%), 31 (47%) and 14 (21%) CHC patients had scores of 1, 2 and 3, respectively. All control subjects scored 0. In both CHC and NASH liver RBP4 scores were directly related to western blot (p = 0.001 and p = 0.03), not to mRNA expression (p = 0.77 and p = 0.40). Older age (OR, 1.07; 95%CI, 1.01–1.13), RBP4 score (4.26; 1.27–14.21) and HOMA (2.26; 1.15–4.42) were independently associated with steatosis ≥10% in CHC patients. In NASH lobular inflammation (OR, 3.77; 95%CI, 1.01–24.22) and RBP4 score (4.87; 1.003–23.65) were the only risk factors for fibrosis ≥2 at logistic regression analysis.ConclusionHepatic storage of RBP4, unrelated to its expression, could cause liver damage both in NASH and CHC.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Digestive and Liver Disease - Volume 43, Issue 5, May 2011, Pages 404–410
نویسندگان
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