High Mobility Group Box 1 in Preterm Infants with Intraventricular Hemorrhage

Jianglin Ma1, Hongyan Lu

  • 1Department of Pediatrics, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, and #Department of Pediatrics, The Affiliated Hospital of Jiangsu University, Zhenjiang, Jiangsu; China. 494462648@qq.com.

Indian Pediatrics
|June 3, 2016
PubMed

Insights

High mobility group box 1 (HMGB1) levels were significantly higher in preterm infants diagnosed with intraventricular hemorrhage (IVH). This finding suggests HMGB1 may play a role in the development of IVH in premature newborns.

Area of Science:

  • Neonatal Medicine
  • Biochemistry
  • Pediatric Neurology

Background:

  • Intraventricular hemorrhage (IVH) is a significant concern in preterm infants, often leading to adverse neurological outcomes.
  • High mobility group box 1 (HMGB1) is a protein known to be involved in inflammatory and cellular processes.
  • The role of HMGB1 in the pathogenesis of neonatal brain injury, specifically IVH, requires further elucidation.

Purpose of the Study:

  • To investigate the association between cord blood levels of high mobility group box 1 (HMGB1) and the presence of intraventricular hemorrhage (IVH) in preterm infants.

Main Methods:

  • Cord blood samples were collected from preterm infants at birth.
  • Concentrations of HMGB1 were quantified using enzyme-linked immunosorbent assay (ELISA).
  • Infants were categorized into two groups: those with diagnosed IVH and those without IVH.

Main Results:

  • The concentration of HMGB1 in cord blood was significantly elevated in preterm infants with IVH compared to those without IVH (P=0.041).
  • This statistically significant difference indicates a potential link between higher HMGB1 levels and the occurrence of IVH.

Conclusions:

  • Elevated cord blood levels of HMGB1 are associated with intraventricular hemorrhage in preterm infants.
  • HMGB1 may serve as a potential biomarker for predicting or understanding the risk of IVH in this vulnerable population.
  • Further research is warranted to explore the mechanistic role of HMGB1 in the development of IVH.