Prenatal and perinatal characteristics associated with pediatric-onset inflammatory bowel disease

Susan Hutfless1, De-Kun Li, Melvin B Heyman

  • 1Division of Gastroenterology and Hepatology, Johns Hopkins University, 600 N. Wolfe St., Blalock Building 449, Baltimore, MD 21287, USA. shutfle1@jhmi.edu

Insights

Maternal inflammatory bowel disease (IBD) and white race are linked to pediatric IBD risk. This study identified key factors by accounting for confounding in early life risk assessments.

Area of Science:

  • Pediatric Gastroenterology
  • Epidemiology
  • Genetics and Genomics

Background:

  • Early life risk factors for pediatric inflammatory bowel disease (IBD) often lack confounding analysis, leading to inaccurate findings.
  • Previous studies have not adequately addressed confounding variables in identifying IBD risk factors.
  • Robust identification of pediatric IBD risk factors requires accounting for potential confounders.

Purpose of the Study:

  • To investigate the association between prenatal and perinatal factors and the risk of pediatric-onset IBD.
  • To rigorously assess risk factors by controlling for potential confounding variables.
  • To clarify the relationship between maternal and infant characteristics and IBD development.

Main Methods:

  • A nested case-control study design was employed.
  • Included 189 pediatric IBD cases (age ≤18) and 3,080 matched controls.
  • Utilized conditional logistic regression on electronic health records for analysis.

Main Results:

  • Maternal history of IBD (OR 5.1) and white race (OR 2.3) were significantly associated with pediatric IBD.
  • Maternal respiratory infection, maternal age <20, and gestational hypertension showed non-significant associations.
  • The study identified statistically significant risk factors after accounting for confounding.

Conclusions:

  • Maternal IBD history and race are key factors associated with pediatric IBD development.
  • The findings are based on a well-documented cohort with confirmed diagnoses.
  • This research provides a more accurate understanding of pediatric IBD etiology.
Abstract

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