α-Defensins and bacterial/permeability-increasing protein as new markers of childhood obesity

A Prats-Puig1,2,3, M Gispert-Saüch1, G Carreras-Badosa1,2

  • 1Dr Josep Trueta Hospital, Girona, Spain.

Pediatric Obesity
|March 2, 2016
PubMed

Insights

Alpha-defensins and bacterial/permeability-increasing protein may serve as indicators of childhood obesity. Higher alpha-defensin levels in children may predict increased body mass index and abdominal fat accumulation.

Area of Science:

  • Pediatric Endocrinology
  • Cardiovascular Health
  • Biomarker Discovery

Background:

  • Childhood obesity is a growing public health concern with long-term cardiovascular implications.
  • Identifying early biomarkers for obesity and associated risks is crucial for timely intervention.

Purpose of the Study:

  • To investigate the association between alpha-defensins (α-defensins) and bacterial/permeability-increasing protein (BPI) with obesity and cardiovascular risk factors in prepubertal children.
  • To determine if these proteins can serve as predictive markers for childhood obesity.

Main Methods:

  • Cross-sectional and longitudinal study designs were employed with a total of 250 and 91 children, respectively.
  • Measurements included plasma α-defensins, BPI, body mass index (BMI), waist circumference, systolic blood pressure (SBP), carotid intima media thickness (cIMT), HOMA-IR, and HMW-adiponectin.

Main Results:

  • Higher α-defensin concentrations positively correlated with BMI, waist circumference, SBP, cIMT, and HOMA-IR, while negatively correlating with HMW-adiponectin in the cross-sectional analysis.
  • BPI concentrations showed inverse associations with these parameters.
  • In the longitudinal study, α-defensins at age 7 predicted BMI and waist circumference at age 10.

Conclusions:

  • α-Defensins and BPI may function as potential biomarkers for childhood obesity.
  • Elevated α-defensin levels could indicate a predisposition to increased BMI and abdominal adiposity in children, suggesting their utility in early risk assessment.
Abstract

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