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Impact of Wisteria floribunda Agglutinin-Positive Mac-2-Binding Protein in Patients with Hepatitis C Virus-Related Compensated Liver Cirrhosis.

Authors :
Kunihiro Hasegawa
Ryo Takata
Hiroki Nishikawa
Hirayuki Enomoto
Akio Ishii
Yoshinori Iwata
Yuho Miyamoto
Noriko Ishii
Yukihisa Yuri
Chikage Nakano
Takashi Nishimura
Kazunori Yoh
Nobuhiro Aizawa
Yoshiyuki Sakai
Naoto Ikeda
Tomoyuki Takashima
Hiroko Iijima
Shuhei Nishiguchi
Source :
International Journal of Molecular Sciences; Sep2016, Vol. 17 Issue 9, p1500, 13p, 3 Charts, 7 Graphs
Publication Year :
2016

Abstract

We aimed to examine the effect of Wisteria floribunda agglutinin-positive Mac-2-binding protein (WFA+-M2BP) level on survival comparing with other laboratory liver fibrosis markers in hepatitis C virus (HCV)-related compensated liver cirrhosis (LC) (n = 165). For assessing prognostic performance of continuous fibrosis markers, we adapted time-dependent receiver operating characteristics (ROC) curves for clinical outcome. In time-dependent ROC analysis, annual area under the ROCs (AUROCs) were plotted. We also calculated the total sum of AUROCs in all time-points (TAAT score) in each fibrosis marker. WFA+-M2BP value ranged from 0.66 cutoff index (COI) to 19.95 COI (median value, 5.29 COI). Using ROC analysis for survival, the optimal cutoff point for WFA+-M2BP was 6.15 COI (AUROC = 0.79348, sensitivity = 80.0%, specificity = 74.78%). The cumulative five-year survival rate in patients with WFA+-M2BP ≥ 6.15 COI (n = 69) was 43.99%, while that in patients with WFA+-M2BP < 6.15 COI (n = 96) was 88.40% (p < 0.0001). In the multivariate analysis, absence of hepatocellular carcinoma (p = 0.0008), WFA+-M2BP < 6.15 COI (p = 0.0132), achievement of sustained virological response (p < 0.0001) and des--carboxy prothrombin < 41 mAU/mL (p = 0.0018) were significant favorable predictors linked to survival. In time-dependent ROC analysis in all cases, WFA+-M2BP had the highest TAAT score among liver fibrosis markers. In conclusion, WFA+-M2BP can be a useful predictor in HCV-related compensated LC. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16616596
Volume :
17
Issue :
9
Database :
Complementary Index
Journal :
International Journal of Molecular Sciences
Publication Type :
Academic Journal
Accession number :
118338868
Full Text :
https://doi.org/10.3390/ijms17091500