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Von Willebrand factor and esophageal varices in children with chronic liver diseases
Mohamed Abdel-Salam El-Guindi1, Nermin Mohammed Adawy1, Iman Shaban Osheba2
1Department of Pediatric Hepatology, Gastroenterology and Nutrition, National Liver Institute, Menoufia University, Shebin El-koom, Menoufia, Egypt.
Insights
High plasma levels of von Willebrand factor antigen (vWF-Ag) can predict esophageal varices (EVs) in children with chronic liver disease (CLD). Elevated vWF-Ag levels correlate with the severity of EVs, offering a valuable prognostic tool.
Area of Science:
- Hepatology
- Pediatric Gastroenterology
- Biomarker Discovery
Background:
- Chronic liver diseases (CLDs) in children can lead to serious complications such as esophageal varices (EVs).
- Accurate prediction of EVs is crucial for timely intervention and management in pediatric CLD patients.
- Non-invasive biomarkers are needed to assess the risk of EVs.
Purpose of the Study:
- To investigate the utility of plasma von Willebrand factor antigen (vWF-Ag) levels as a predictor for the presence of EVs in children with CLDs.
- To assess the correlation between vWF-Ag levels and the grade of EVs.
Main Methods:
- A cohort of 50 children with CLD underwent upper esophagogastroduodenoscopy (EGD) to diagnose EVs.
- Plasma vWF-Ag levels, Child-Pugh score (CPS), and other relevant clinical and laboratory parameters were analyzed.
- Receiver operating characteristic (ROC) analysis was used to determine the accuracy of vWF-Ag in predicting EVs.
Main Results:
- Plasma vWF-Ag demonstrated high accuracy (74%) in discriminating the presence of EVs at a cut-off of 108.99 IU/ml (p < 0.0001).
- Higher vWF-Ag levels were significantly associated with the presence and increased grade of EVs.
- The VITRO score also showed good accuracy (80%) in detecting EVs.
Conclusions:
- Elevated plasma vWF-Ag is a valuable prognostic marker for identifying children with CLD who are at risk of developing EVs.
- vWF-Ag levels correlate with the severity of esophageal varices, aiding in risk stratification.
- This finding supports the potential use of vWF-Ag as a non-invasive tool in managing pediatric CLD.
Aim Of The Study:
To evaluate the role of plasma level of von Willebrand factor antigen (vWF-Ag) as a possible predictor for the presence of esophageal varices (EVs) in children with chronic liver diseases (CLDs).
Material And Methods:
All patients underwent upper esophagogastroduodenoscopy (EGD) and were categorized as group I (had EVs) and group II (had no EVs). The following patient data were determined: Child-Pugh score (CPS), plasma vWF-Ag, vWF-Ag/thrombocyte ratio (VITRO) score, aspartate transaminase (AST) to platelet ratio index (APRI) score, AST/alanine transaminase (ALT), platelet count/spleen diameter, grading of EVs (small, medium and large) and categorizing the stage of liver fibrosis.
Results:
The analysis included 50 patients with CLD; 30 (60%) were female. The commonest etiological diagnoses were autoimmune hepatitis (AIH) (20%) and extra-hepatic biliary atresia (EHBA) (12%). 26% of cases were categorized as undiagnosed CLD. The CPS showed CPS-A 34%, CPS-B 44% and CPS-C 22%. The vWF-Ag was found at a high level of 243.52 ±195.97, with a highly statistically significant difference in discriminating the EVs with 74% accuracy at a cut-off value of 108.99 IU/ml, p < 0.0001. Also, ROC analysis was performed for discriminating large esophageal varices with 84% accuracy at a cut-off value of 475.85 mg%. The VITRO score at a cut-off value of 1.72 could detect EVs with 70% sensitivity, 86.7% specificity, and 80% accuracy.
Conclusions:
High vWF-Ag is a valuable prognostic tool for estimating the presence of EVs, and higher vWF-Ag is associated with increased grade of EVs.
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