4.1 Article

Serum Mac-2 binding protein levels as a novel diagnostic biomarker for prediction of disease severity and nonalcoholic steatohepatitis

Journal

PROTEOMICS CLINICAL APPLICATIONS
Volume 7, Issue 9-10, Pages 648-656

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/prca.201200137

Keywords

Ballooning hepatocyte; Liver fibrosis; Mac-2bp/90K; N-glycan; NASH/NAFLD

Funding

  1. Japan Society for the Promotion of Science [21249038, 24590972]
  2. Global COE Program of Osaka University
  3. Ministry of Education, Culture, Sports, Science, and Technology of Japan
  4. Grants-in-Aid for Scientific Research [23590974, 21249038, 24590972] Funding Source: KAKEN

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PurposeMac-2 binding protein (Mac-2bp) is one of the major fucosylated glycoproteins, which we identified with glycol-proteomic analyses. We previously reported that fucosylated glycoproteins are secreted into bile, but scarcely secreted into sera in normal liver and hypothesized that the fucosylation-based sorting machinery would be disrupted in ballooning hepatocytes due to the loss of cellular polarity. In the present study, we investigated the availability of Mac-2bp for differential diagnosis of nonalcoholic steatohepatitis (NASH) from nonalcoholic fatty liver disease (NAFLD) as a biomarker. Experimental designSerum Mac-2bp levels were determined with our developed ELISA kit. Our cohort of 127 patients with NAFLD had liver biopsy to make a histological diagnosis of NASH and simple fatty liver. ResultsMac-2bp levels were significantly elevated in NASH patients compared with non-NASH (simple steatosis) patients (2.132 1.237 vs. 1.103 +/- 0.500 g/mL, p < 0.01). The area under the receiver-operating characteristic curve for predicting NASH by Mac-2bp was 0.816. Moreover, multivariate logistic regression analyses showed Mac-2bp levels could predict the fibrosis stage and the presence of ballooning hepatocytes in NAFLD patients. Conclusions and clinical relevanceThese results support the potential usefulness of measuring Mac-2bp levels in clinical practice as a biomarker for NASH.

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