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Wisteria floribunda agglutinin-positive Mac-2 binding protein predicts the development of hepatocellular carcinoma in patients with nonalcoholic fatty liver disease

As it is not practical to survey hepatocellular carcinoma (HCC) in all patients with nonalcoholic fatty liver disease (NAFLD), there is a need to identify NAFLD patients who are at high risk for HCC. Wisteria floribunda agglutinin-positive Mac-2 binding protein (WFA -M2BP) has been demonstrated to b...

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Bibliographic Details
Published in:Hepatology research 2018-01
Main Authors: Kawanaka, Miwa, Tomiyama, Yasuyuki, Hyogo, Hideyuki, Koda, Masahiko, Shima, Toshihide, Tobita, Hiroshi, Hiramatsu, Akira, Nishino, Ken, Okamoto, Toshiaki, Sato, Shuichi, Hara, Yuichi, Nishina, Sohji, Kawamoto, Hirofumi, Chayama, Kazuaki, Okanoue, Takeshi, Hino, Keisuke
Format: Article
Language:English
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Summary:As it is not practical to survey hepatocellular carcinoma (HCC) in all patients with nonalcoholic fatty liver disease (NAFLD), there is a need to identify NAFLD patients who are at high risk for HCC. Wisteria floribunda agglutinin-positive Mac-2 binding protein (WFA -M2BP) has been demonstrated to be a surrogate marker for predicting HCC as well as a liver fibrosis marker in patients with chronic hepatitis B and C. The aim of this study was to investigate whether WFA -M2BP predicts HCC development in NAFLD patients. Serum WFA -M2BP was retrospectively measured in 331 patients with histologically proven NAFLD, 51 of whom developed HCC. The association of WFA -M2BP and HCC development in NAFLD patients was investigated. WFA -M2BP values were significantly greater in NAFLD patients with HCC than in those without HCC among patients with liver fibrosis ≥stage 3. Multivariate analysis identified WFA -M2BP as one of the predictive factors for HCC development (OR: 1.57, 95% CI: 1.083-2.265, P=0.017). The optimal cutoff index of WFA -M2BP for predicting HCC was 1.255 with specificity of 78.4% and sensitivity of 70.4%. The area under the receiver operating characteristic curve value for the prediction of HCC development was 0.806. The cumulative incidence rate of HCC was significantly greater in patients with WFA -M2BP≥1.255 (n=61) than in those with WFA -M2BP
ISSN:1386-6346
DOI:10.1111/hepr.13054