# Role of plasma Von-Willebrand factor in children with chronic liver diseases

**Authors:** Ola Galal Ali Behairy, Abdelhamid Mohamed El-Hamshary, Ahmed Adel Torky, Rana Atef Khashaba, Basma Galal Ali, Nashwa Farouk Mohamed

PMC · DOI: 10.1007/s00431-025-06355-7 · European Journal of Pediatrics · 2025-08-05

## TL;DR

This study explores plasma Von-Willebrand Factor (VWF Ag) as a non-invasive tool to assess liver fibrosis severity in children with chronic liver disease.

## Contribution

VWF Ag is proposed as a new non-invasive biomarker for liver fibrosis grading in pediatric chronic liver disease.

## Key findings

- VWF Ag levels were significantly higher in children with chronic liver disease compared to healthy controls.
- VWF Ag strongly correlates with fibrosis scores and histological stages in children.
- VWF Ag shows high sensitivity and specificity for detecting mild and severe fibrosis.

## Abstract

Children with chronic liver diseases (CLD) face more significant clinical problems. The most reliable technique for detecting liver fibrosis is still liver biopsy (LB). Our investigation assessed Von-Willebrand Factor Antigen (VWF Ag) plasma titer as a probable non-invasive predictor for grading liver fibrosis in children with CLD. 120 children participated in our case–control study, 60 of whom had CLD and the remaining 60 of whom were healthy. Underlying etiologies were diagnosed via clinical, biochemical, and histological criteria by LB. VWF Ag concentrations were determined in all participants using enzyme-linked immunosorbent assay (ELISA). VWF Ag mean titers were significantly elevated in CLD cases in contrast with controls (581.4 ± 279 vs. 166.9 ± 78 ng/ml; P < 0.001). There was a remarkable positive association amongst VWF Ag and total, direct serum bilirubin (TSB, DSB), aspartate aminotransferase (AST), alanine aminotransferase (ALT), liver span, portal hypertension, Model for End-Stage Liver Disease (MELD) score, Pediatric End-Stage Liver Disease (PELD) score, and Child–Pugh score (P ≤ 0.05). VWF Ag anticipated mild (AUC 0.973, cutoff > 266.5 ng/ml) and severe fibrosis (AUC 0.988, cutoff > 590.3 ng/ml) with sensitivity and specificity of 100% and 86.7% for mild fibrosis and 100% and 92.9% for severe fibrosis, respectively.

Conclusion: VWF Ag can serve as a significant indicator of liver fibrosis severity in pediatric CLD cases.
What is Known:• Liver biopsy remains the cornerstone for diagnosing and staging liver fibrosis in children.What is New:• VWF Ag is a promising non-invasive indicator for grading liver fibrosis severity in pediatric chronic liver disease.• VWF Ag correlates strongly with fibrosis scores as Child–Pugh, MELD, PELD, AST/PLT ratio index (APRI), and fibrosis-4 (FIB-4), and histological fibrosis stages (by ISHAK score) in children.

What is Known:

• Liver biopsy remains the cornerstone for diagnosing and staging liver fibrosis in children.

What is New:

• VWF Ag is a promising non-invasive indicator for grading liver fibrosis severity in pediatric chronic liver disease.

• VWF Ag correlates strongly with fibrosis scores as Child–Pugh, MELD, PELD, AST/PLT ratio index (APRI), and fibrosis-4 (FIB-4), and histological fibrosis stages (by ISHAK score) in children.

## Full-text entities

- **Genes:** VWF (von Willebrand factor) [NCBI Gene 7450] {aka F8VWF, VWD}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}
- **Diseases:** fibrosis (MESH:D005355), End-Stage Liver Disease (MESH:D058625), CLD (MESH:D008107), liver fibrosis (MESH:D008103), portal hypertension (MESH:D006975)
- **Chemicals:** bilirubin (MESH:D001663)

## Full text

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## Figures

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## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC12325533/full.md

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Source: https://tomesphere.com/paper/PMC12325533