Maternal risk factors vary between subpopulations of children with autism spectrum disorder

Genevieve Grivas1,2,3, Richard E Frye4,5, Juergen Hahn1,2,6

  • 1Department of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, New York, USA.

Insights

Prenatal risk factors for autism spectrum disorder (ASD) subgroups with co-occurring conditions (COCs) were identified. Distinct risk factors emerged for each subgroup, supporting ASD classification by COCs.

Area of Science:

  • Developmental Pediatrics
  • Autism Spectrum Disorder Research
  • Prenatal Risk Factor Analysis

Background:

  • Previous research classified children with autism spectrum disorder (ASD) into three subgroups based on co-occurring conditions (COCs) within the first five years of life.
  • Understanding the prenatal origins of these subgroups is crucial for addressing ASD heterogeneity.

Purpose of the Study:

  • To investigate distinct prenatal risk factors associated with three previously identified ASD subgroups: High-Prevalence COCs, Developmental Delay/Seizure (DD/Seizure) COCs, and Low-Prevalence COCs.
  • To determine if prenatal risk factors differ across these ASD subgroups.

Main Methods:

  • Utilized maternal medical claims data to identify prenatal risk factors.
  • Analyzed risk factors in relation to the three distinct ASD subgroups defined by co-occurring conditions.

Main Results:

  • Identified shared and unique prenatal risk factors across the three ASD subgroups.
  • High-Prevalence COCs subgroup associated with infections, anti-inflammatory, and complex medications.
  • DD/Seizure COCs subgroup linked to immune deregulatory conditions (e.g., asthma, joint disorders).
  • Low-Prevalence COCs subgroup associated with overall pregnancy complications.

Conclusions:

  • Children with ASD exhibit distinct prenatal risk factor profiles corresponding to their co-occurring condition subgroups.
  • Subgrouping children with ASD based on COCs provides a potential framework for understanding ASD heterogeneity.
  • Findings support the clinical relevance of identifying specific prenatal exposures for different ASD presentations.

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