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Radiologic Nonalcoholic Fatty Liver Disease Increases the Risk of Hepatocellular Carcinoma in Patients with Suppressed Chronic Hepatitis B

Authors
Cho, H.Chang, Y.Lee, J.-H.Cho, Y.Y.Nam, J.Y.Lee, Y.B.Lee, D.H.Cho, E.J.Yu, S.J.Kim, Y.J.Lee, J.M.Yoon, J.-H.
Issue Date
Aug-2020
Publisher
Lippincott Williams and Wilkins
Keywords
biochemical response; chronic hepatitis B; hepatocellular carcinoma; nonalcoholic fatty liver disease; virological suppression
Citation
Journal of Clinical Gastroenterology, v.54, no.7, pp 633 - 641
Pages
9
Journal Title
Journal of Clinical Gastroenterology
Volume
54
Number
7
Start Page
633
End Page
641
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/44158
DOI
10.1097/MCG.0000000000001217
ISSN
0192-0790
1539-2031
Abstract
Background and Goals: Although nonalcoholic fatty liver disease (NAFLD) is a risk factor of hepatocellular carcinoma (HCC), it is unclear whether NAFLD additionally increases the risk of HCC among chronic hepatitis B (CHB) patients. This study evaluated the association between NAFLD and the risk of HCC in patients whose hepatitis B virus (HBV) was well controlled. Study: This study included consecutive CHB patients whose serum HBV DNA levels were continuously suppressed <2000 IU/mL with antiviral treatment. Fatty liver was radiologically diagnosed. Patients with concomitant hepatitis C infection, autoimmune hepatitis, or excessive alcohol use were excluded. Results: Among 826 patients, 86 patients (10.4%) developed HCC during the study period (median, 43.1 mo). The patients with NAFLD (N=260) had a significantly higher risk for HCC compared with patients without NAFLD (N=566) (adjusted hazard ratio, 1.67; 95% confidence interval, 1.05-2.63; P=0.03) after adjustment for age, the presence of cirrhosis, hepatitis B envelop antigen positivity, low-level viremia and hypertension. There was significant association between incomplete biochemical response (IBR) (alanine aminotransferase levels ≥40 IU/L) and the presence of NAFLD (P<0.001 by χ 2 test). IBR at the time of virological response was associated with a significantly higher risk of HCC development (adjusted hazard ratio, 1.63; 95% confidence interval, 1.06-2.54; P=0.03). Conclusions: NAFLD increases the risk of HCC in patients with CHB in whom HBV is effectively suppressed by antivirals. Patients with IBR should be suspected of concurrent NAFLD. Further study is warranted to evaluate whether improvement of NAFLD might decrease the risk of HCC development. © 2019 Lippincott Williams and Wilkins. All Rights Reserved.
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의과대학 (의학부(임상-서울))
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