Maternal obesity associated with inflammation in their children

Karen L Leibowitz1, Reneé H Moore, Rexford S Ahima

  • 1The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA. leibowka@umdnj.edu

Insights

Maternal obesity during pregnancy is linked to higher levels of high-sensitivity C-reactive protein (hs-CRP) in offspring. This inflammatory marker elevation persists even after accounting for the child's weight.

Area of Science:

  • Pediatric Health
  • Maternal-Fetal Medicine
  • Inflammation Research

Background:

  • Maternal obesity is a growing concern with potential long-term health implications for offspring.
  • Inflammatory markers and adiponectin are key indicators of metabolic and inflammatory states.

Purpose of the Study:

  • To investigate the association between maternal pre-pregnancy obesity and specific inflammatory markers (TNF-α, IL-6, hs-CRP) and adiponectin in 12-year-old offspring.
  • To determine if maternal obesity influences these biomarkers in children, adjusting for potential confounders.

Main Methods:

  • Thirty-four children from the Infant Growth Study were assessed at age 12.
  • Participants were categorized into high-risk (HR) and low-risk (LR) groups based on maternal pre-pregnancy BMI.
  • Measurements included weight, height, Tanner stage, and key biomarkers.

Main Results:

  • Children in the HR group showed significantly higher levels of high-sensitivity C-reactive protein (hs-CRP) compared to the LR group.
  • No significant group differences were observed for tumor necrosis factor-α, interleukin-6, or adiponectin.
  • The odds of HR children having detectable hs-CRP were 16 times greater than LR children, even after adjusting for BMI z-score, Tanner stage, and gender.

Conclusions:

  • Maternal obesity during pregnancy is associated with an increased risk of elevated hs-CRP in offspring.
  • This association remains significant even when controlling for the child's current weight status.
  • Early life inflammatory profiles may be influenced by the maternal metabolic environment during gestation.
Abstract

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