Plasma human growth cytokines in children with vasovagal syncope

Yuanyuan Wang1, Yaru Wang1, Bing He2

  • 1Department of Pediatrics, Peking University First Hospital, Beijing, China.

Insights

Plasma human growth cytokines are altered in pediatric vasovagal syncope (VVS). Elevated hepatocyte growth factor (HGF) and insulin-like growth factor binding protein-1 (IGFBP-1), with decreased epidermal growth factor (EGF), are linked to VVS development and diagnosis.

Area of Science:

  • Pediatric Cardiology
  • Endocrinology
  • Biochemistry

Background:

  • Vasovagal syncope (VVS) is a common cause of syncope in children.
  • The underlying pathophysiological mechanisms of VVS are not fully understood.
  • Growth factors play crucial roles in various physiological processes and may be implicated in VVS.

Purpose of the Study:

  • To investigate the profile of plasma human growth cytokines in children with VVS.
  • To identify specific growth factors associated with the development of pediatric VVS.
  • To evaluate the diagnostic potential of these growth factors for VVS.

Main Methods:

  • Plasma samples from VVS children and healthy controls were analyzed using cytokine arrays.
  • Discovery and validation sets were employed to identify and confirm differential cytokine levels.
  • Statistical analyses, including hierarchical clustering, logistic regression, and ROC curve analysis, were performed.

Main Results:

  • Children with VVS showed altered plasma levels of several growth factors compared to controls.
  • Significantly higher concentrations of hepatocyte growth factor (HGF) and insulin-like growth factor binding protein-1 (IGFBP-1) were observed in VVS patients.
  • Lower concentrations of epidermal growth factor (EGF) were found in pediatric VVS patients.

Conclusions:

  • Plasma human growth cytokine profiles are altered in pediatric VVS.
  • Elevated HGF and IGFBP-1, and decreased EGF are associated with pediatric VVS development.
  • These three proteins show potential as diagnostic biomarkers for pediatric VVS.
Abstract

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