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Use of the Serum Wisteria floribunda Agglutinin-Positive Mac2 Binding Protein as a Marker of Gastroesophageal Varices and Liver-Related Events in Chronic Hepatitis C Patients
A test to narrow down patients who require esophagogastroduodenoscopy (EGD) with a high probability of having gastroesophageal varices (GEV) and a high-risk of liver-related events is an unmet need. The measurement of serum fibrosis markers and EGD was performed in 166 consecutive chronic hepatitis...
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Published in: | Diagnostics (Basel) 2020-03, Vol.10 (3), p.173 |
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Main Authors: | , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A test to narrow down patients who require esophagogastroduodenoscopy (EGD) with a high probability of having gastroesophageal varices (GEV) and a high-risk of liver-related events is an unmet need.
The measurement of serum fibrosis markers and EGD was performed in 166 consecutive chronic hepatitis C patients. The correlation between the grades of GEV and fibrosis markers and the subsequent occurrence of liver-related and fibrosis markers were examined.
agglutinin-positive human Mac-2 binding protein (WFA
-M2BP) levels increased according to the grade of GEV (3.4 (0.2-18.6) for no GEV, 7.9 (1.8-20.0) for small GEV, and 11.4 (4.0-20.0) for large GEV;
< 0.001). The diagnostic accuracy of the WFA
-M2BP was superior compared to other serum fibrosis markers, and WFA
-M2BP was an independent predictor of GEV in the multivariate analysis. Furthermore, the cumulative incidence of liver-related events at one year was 2.3% in patients with WFA
-M2BP levels ≤ 7.0 and 37.5% in patients with WFA
-M2BP levels > 7.0 (
< 0.001). WFA
-M2BP > 7.0 was a significant predictive factor for liver-related events (Hazard ratio 6.7,
= 0.004) independent of Child-Pughclass.
WFA
-M2BP could be used to estimate the presence and grade of GEV and is linked to liver-related events in chronic hepatitis C patients. |
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ISSN: | 2075-4418 2075-4418 |
DOI: | 10.3390/diagnostics10030173 |