Insulin resistance and oxidative stress in children born small and large for gestational age

Pediatrics. 2009 Aug;124(2):695-702. doi: 10.1542/peds.2008-3056. Epub 2009 Jul 27.

Abstract

Objective: Our aim was to evaluate the effect of BW and obesity on oxidative stress and IR in prepubertal SGA and LGA children compared with appropriate-for-gestational-age (AGA) children.

Methods: We performed a cross-sectional study comparing oxidative stress and IR in 103 children categorized into 6 groups according to BW (26 SGA, 15 AGA, and 16 LGA normal-weight children) and obesity (15 SGA, 15 AGA, and 16 LGA obese children). Indexes of IR (HOMA-IR, G/I) and the marker of oxidative stress (urinary isoprostanes) were evaluated.

Results: Homeostasis Model Assessment was higher in both normal-weight SGA and LGA children than in normal-weight AGA children (all P <or= .02). Furthermore, a difference was detected between obese SGA and obese LGA subjects compared with normal-weight SGA (all P <or= .0007) and LGA (all P <or= .01) children, respectively. The G/I ratio was lower in the 3 obese groups than normal-weight AGA (all P <or= .009) and normal-weight SGA children (all P <or= .02). Furthermore, a difference was detected between obese SGA and obese LGA children compared with normal-weight LGA children (all P <or= .0002). Isoprostane levels were higher in both normal-weight SGA and LGA children than in normal-weight AGA children (all P <or= .002). Moreover, both obese SGA and LGA children showed higher levels than obese AGA children (all P <or= .01) and in comparison to the 3 normal-weight groups (all P <or= .04).

Conclusion: Increased IR and oxidative stress are already present in prepubertal normal-weight SGA and LGA children with a continuous alteration in relation to obesity, suggesting that BW and adiposity represent 2 independent risk factors for degenerative diseases.

Publication types

  • Comparative Study

MeSH terms

  • Anthropometry
  • Birth Weight
  • Child
  • Child, Preschool
  • Cross-Sectional Studies
  • Dinoprost / blood
  • Female
  • Fetal Macrosomia / epidemiology
  • Fetal Macrosomia / physiopathology*
  • Humans
  • Infant
  • Infant, Newborn
  • Infant, Small for Gestational Age*
  • Insulin Resistance / physiology*
  • Isoprostanes / urine
  • Longitudinal Studies
  • Male
  • Obesity / epidemiology
  • Obesity / physiopathology*
  • Oxidative Stress / physiology*
  • Pregnancy
  • Reference Values
  • Regression Analysis
  • Risk Factors

Substances

  • Isoprostanes
  • Dinoprost