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Serum WFA -M2BP levels for evaluation of early stages of liver fibrosis in patients with chronic hepatitis B virus infection. | LitMetric

AI Article Synopsis

Article Abstract

Background & Aims: Accurate evaluation of liver fibrosis is crucial for predicting progression of chronic hepatitis B virus (HBV) infection. We assessed the utility of a novel fibrosis glycobiomarker Wisteria floribunda agglutinin-positive Mac-2-binding protein (WFA -M2BP) for evaluating liver fibrosis and disease progression in patients with chronic HBV infection.

Methods: We enrolled 774 patients with chronic HBV infection, with or without fibrosis, diagnosed by liver biopsy/FibroScan. Patients who underwent liver biopsy (n = 297) were divided into training (n = 221) and validation (n = 76) groups. Serum WFA -M2BP values were measured and compared with FIB-4 index, aspartate aminotransferase (AST)-to-platelet ratio (APRI) and AST-to-alanine aminotransferase ratio (AAR) using receiver-operating characteristic (ROC) analysis.

Results: Serum WFA -M2BP levels increased significantly with fibrosis progression (P < 0.0001). Area under the ROC curve of WFA -M2BP for diagnosing significant fibrosis was higher than that of FIB-4 (P = 0.198), APRI (P = 0.017) and AAR (P < 0.001), with sensitivity and specificity in the training set of 60.5% and 79.8% and validation set of 59.5% and 82.1%, respectively. Serum WFA -M2BP levels were significantly correlated with FibroScan values (P < 0.0001) and improved the accuracy of FibroScan in assessing significant fibrosis. Changes in WFA -M2BP levels were parallel with those in FibroScan values during nucleot(s)ide analogues therapy in patients with chronic HBV infection.

Conclusions: WFA -M2BP is an accurate serum indicator for assessing early stages of liver fibrosis and may monitor regression of fibrosis during the treatment of chronic HBV infection. WFA -M2BP provides a simple and reliable alternative or complementary method to liver biopsy and FibroScan.

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http://dx.doi.org/10.1111/liv.13188DOI Listing

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