[Changes of serum leptin and vascular endothelial growth factor in children with congenital heart disease]

Yuan-Hai Zhang1, Ru-Lian Xiang, Xing-Ti Hu

  • 1Department of Pediatrics, Yuying Children's Hospital Affiliated to Wenzhou Medical College, Wenzhou, Zhejiang 325027, China. zyh265@yahoo.com.cn

Insights

Serum leptin (LEP) and vascular endothelial growth factor (VEGF) are elevated in children with congenital heart disease (CHD). These factors are linked to disease severity and heart failure development in pediatric CHD patients.

Area of Science:

  • Pediatric Cardiology
  • Biomarkers in Congenital Heart Disease
  • Vascular Biology

Context:

  • Congenital heart disease (CHD) encompasses a range of structural abnormalities present at birth.
  • Understanding the underlying pathophysiology of CHD is crucial for effective management and treatment.
  • Biomarkers that reflect disease activity and progression are needed for pediatric cardiology.

Purpose:

  • To investigate serum levels of leptin (LEP) and vascular endothelial growth factor (VEGF) in children with CHD.
  • To determine the association of LEP and VEGF with different types of CHD and heart failure.
  • To explore the roles of LEP and VEGF in the pathobiology of pediatric CHD.

Summary:

  • Children with congenital heart disease (CHD) exhibited significantly higher serum levels of leptin (LEP) and vascular endothelial growth factor (VEGF) compared to healthy controls.
  • Elevated LEP and VEGF levels, along with an increased LEP/BMI ratio, were observed in both acyanotic and cyanotic CHD groups, particularly in those with heart failure.
  • Serum LEP correlated positively with BMI in acyanotic CHD, while in cyanotic CHD, LEP correlated with VEGF and hemoglobin, and both VEGF and LEP negatively correlated with arterial oxygen saturation.

Impact:

  • This study identifies LEP and VEGF as potential biomarkers for CHD severity and progression in children.
  • Findings suggest that VEGF and LEP contribute to the pathophysiology of CHD and are associated with heart failure development in acyanotic CHD.
  • These insights may pave the way for novel therapeutic strategies targeting VEGF and LEP pathways in pediatric cardiovascular diseases.
Abstract

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