Concentrations of leptin, adiponectin and other metabolic parameters in non-obese children with Down syndrome

Insights

Children with Down syndrome (DS) show higher leptin levels and leptin resistance, potential early indicators for cardiovascular disease (CVD) risk. Further research is needed to understand these cardiometabolic changes in DS.

Area of Science:

  • Pediatric Endocrinology
  • Cardiovascular Disease Research
  • Genetics and Metabolism

Background:

  • Adults with Down syndrome (DS) face elevated cardiovascular disease (CVD) risks, impacting morbidity and mortality.
  • Identifying childhood cardiometabolic risk factors in DS is crucial for early intervention strategies.
  • Limited data exists on cardiometabolic risk factors in children with DS.

Purpose of the Study:

  • To investigate cardiometabolic risk factors in non-obese children with DS.
  • To assess insulin resistance (IR), leptin, adiponectin, lipid profiles, and leptin resistance.
  • To compare these factors between children with DS and healthy controls.

Main Methods:

  • Cross-sectional case-control study of karyotype-confirmed trisomy-21 DS children (ages 2-12) and matched controls.
  • Detailed anthropometry including BMI standard deviation scores (SDSs).
  • Laboratory analysis of fasting lipids, insulin, glucose, leptin, adiponectin; HOMA-IR for insulin resistance; and leptin/BMI ratio for leptin resistance.

Main Results:

  • Children with DS exhibited significantly higher mean leptin concentrations and leptin resistance indices compared to controls.
  • While adiponectin and glucose levels showed non-significant trends towards lower and higher values, respectively, in the DS group.
  • Insulin, lipid parameters, and HOMA-IR were similar between groups; however, some DS children had elevated leptin or impaired fasting glucose.

Conclusions:

  • Children with DS present altered cardiometabolic risk factors, notably elevated leptin and leptin resistance.
  • Hyperleptinemia without hyperinsulinemia in DS suggests a potential genetic basis for increased leptin resistance.
  • Further investigation into leptin resistance in DS is warranted to address increased CVD risk.
Abstract