Expression of vascular endothelial growth factor A in liver tissues of infants with biliary atresia

Alif Allam1, Mohammed El-Guindi1, Hatem Konsowa1

  • 1National Liver Institute, Menoufia University, Shebin El-koom, Menoufia, Egypt.

Insights

Vascular endothelial growth factor A (VEGF-A) is highly expressed in infants with biliary atresia (BA). This finding, along with cytokeratin 7 (CK7) expression, aids in differentiating BA from other cholestatic conditions.

Area of Science:

  • Pediatric Hepatology
  • Gastroenterology
  • Developmental Biology

Background:

  • Biliary atresia (BA) is a severe neonatal cholestatic liver disease.
  • Accurate diagnosis of BA is crucial for timely intervention and improved outcomes.
  • VEGF-A and CK7 are potential biomarkers in liver diseases.

Purpose of the Study:

  • To assess hepatic expression of vascular endothelial growth factor A (VEGF-A) in infants with BA.
  • To evaluate the diagnostic accuracy of VEGF-A and cytokeratin 7 (CK7) in distinguishing BA from other causes of infantile cholestasis.

Main Methods:

  • Retrospective study of 35 infants with BA and 38 infants with non-BA cholestasis.
  • Immunohistochemical analysis of liver tissues for VEGF-A and CK7 expression.
  • Diagnosis of BA confirmed by intraoperative cholangiography.

Main Results:

  • Significantly higher VEGF-A expression in bile ducts (80%) and arterial walls (77.2%) in BA group compared to non-BA group (p < 0.0001).
  • VEGF-A expression in portal structures showed high accuracy (84.9% for bile ducts, 82.19% for arterial walls) in differentiating BA.
  • Elevated CK7 expression (grade II/III) was observed in the majority of BA patients, with >25% liver tissue expression having 80.8% accuracy.

Conclusions:

  • Hepatic VEGF-A expression in portal structures is a valuable biomarker for diagnosing biliary atresia.
  • Combined assessment of VEGF-A and CK7 expression enhances diagnostic accuracy for BA in infants.
  • VEGF-A and CK7 show promise as diagnostic tools in pediatric liver diseases.
Abstract

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