Association between autism spectrum disorder and inflammatory bowel disease: A systematic review and meta-analysis

Jong Yeob Kim1, Min Je Choi1, Sungji Ha2

  • 1Yonsei University College of Medicine, Seoul, South Korea.

Insights

Individuals with autism spectrum disorder (ASD) have a significantly higher likelihood of developing inflammatory bowel disease (IBD), including ulcerative colitis and Crohn's disease. This finding underscores the importance of screening for IBD in ASD patients.

Area of Science:

  • Gastroenterology
  • Neurodevelopmental Disorders
  • Epidemiology

Background:

  • Autism spectrum disorder (ASD) is increasingly recognized with co-occurring medical conditions.
  • Inflammatory bowel disease (IBD) is one such condition observed in individuals with ASD.

Purpose of the Study:

  • To systematically review and meta-analyze the association between ASD and the subsequent development of IBD.
  • To quantify the risk of IBD in individuals diagnosed with ASD.

Main Methods:

  • A systematic review and random-effects meta-analysis of observational studies.
  • Searches conducted in PubMed, Embase, and PsycInfo, supplemented by manual searches.
  • Inclusion of studies reporting on the association between ASD and IBD, analyzing over 11 million participants across eight datasets.

Main Results:

  • A significant association was found between ASD and subsequent incident IBD (OR = 1.66, p < 0.001), including ulcerative colitis (OR = 1.91, p < 0.001) and Crohn's disease (OR = 1.47, p = 0.002).
  • The association persisted regardless of the temporal sequence of diagnosis.
  • Sensitivity analyses and quality assessments confirmed the robustness of the findings; no publication bias was detected.

Conclusions:

  • Individuals with ASD exhibit a significantly elevated risk for developing IBD.
  • Clinical guidelines should consider screening for IBD in individuals with ASD.
  • Further research is warranted to identify high-risk subgroups within the ASD population and to elucidate shared biological mechanisms.

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