4.8 Article

Race, insulin resistance and hepatic steatosis in chronic hepatitis C

期刊

HEPATOLOGY
卷 45, 期 1, 页码 80-87

出版社

WILEY
DOI: 10.1002/hep.21455

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资金

  1. NATIONAL CENTER FOR RESEARCH RESOURCES [M01RR016500, M01RR000046, M01RR000042, M01RR000645] Funding Source: NIH RePORTER
  2. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [U01DK060349, U01DK060329, U01DK060335, U01DK060324, U01DK060345, U01DK060346, U01DK060340, U01DK060352, U01DK060342, U01DK060309, U01DK060341, U01DK060344, U01DK060327] Funding Source: NIH RePORTER
  3. NCRR NIH HHS [M01 RR00645, M01 RR000042, M01 RR00046, M01 RR16500, M02 RR000079] Funding Source: Medline
  4. NIDDK NIH HHS [U01 DK60327, U01 DK60324, U01 DK60309, U01 DK60344, U01 DK60345, U01 DK60346, U01 DK60349, U01 DK60352, U01 DK60329, U01 DK60335, U01 DK60340, U01 DK60341, U01 DK60342] Funding Source: Medline

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Hepatic steatosis is common in chronic hepatitis C and has been linked to concurrent obesity, insulin resistance, diabetes, disease severity, and poor response to therapy. Racial differences in rates of obesity and diabetes may contribute to racial differences in hepatic steatosis and treatment response. The aim of the present study was to compare hepatic steatosis and its associations between African American (AA) and Caucasian American (CA) patients with chronic hepatitis C, genotype 1, participating in a prospective study of peginterferon and ribavirin therapy. Liver biopsy results were available from 194 AA patients and 205 CA patients. The 2 groups were compared for anthropometric, clinical, and biochemical features and insulin resistance estimated by the homeostasis model assessment index (HOMA-IR). Sixty-one percent of the AA patients and 65% of the CA patients had hepatic steatosis (P = 0.38). In univariable analysis, steatosis was associated with HOMA-IR, body mass index, waist circumference, serum triglycerides, aminotransferase level, and histological scores for inflammation and fibrosis. After adjusting for these features, AA patients had a lower risk of steatosis than did CA patients (OR 0.54, 95% CI 0.32-0.91, P = 0.02). Insulin resistance but not steatosis was associated with a lower rate of sustained virological response when adjusted for known factors that predict response (relative risk 0.87, 95% CI 0.77-0-99, P = 0.028). Conclusion: After adjusting for the higher prevalence of features associated with hepatic steatosis, AA patients had a lower prevalence of hepatic steatosis than did CA patients with chronic hepatitis C, genotype 1. Insulin resistance but not steatosis was independently associated with lower sustained virological response.

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