Risks for nonaffective psychotic disorder and bipolar disorder in young people with autism spectrum disorder: a

Jean-Paul Selten1, Michael Lundberg2, Dheeraj Rai3

  • 1School for Mental Health and Neuroscience, Maastricht University, Maastricht, the Netherlands2Rivierduinen Psychiatric Institute, Leiden, the Netherlands.

JAMA Psychiatry
|March 26, 2015
PubMed

Insights

Individuals with autism spectrum disorder (ASD) have a significantly higher risk for nonaffective psychotic disorder (NAPD) and bipolar disorder (BD). This increased risk was also observed in their siblings, suggesting a potential genetic link.

Area of Science:

  • Psychiatry
  • Neurodevelopmental Disorders
  • Genetics

Background:

  • The co-occurrence of autism spectrum disorder (ASD) with nonaffective psychotic disorder (NAPD) and bipolar disorder (BD) is not well-established.
  • Understanding these associations is crucial for comprehensive patient care and management.

Purpose of the Study:

  • To investigate the risk of NAPD and BD in individuals diagnosed with ASD.
  • To compare these risks with those in their unaffected siblings.

Main Methods:

  • A nested case-control study was conducted using the Stockholm Youth Cohort (n=9062).
  • Individuals diagnosed with ASD (with and without intellectual disability) and their full siblings were followed up using Swedish registers.
  • Adjusted odds ratios (ORs) were calculated for NAPD and BD.

Main Results:

  • Individuals with ASD showed substantially increased adjusted ORs for NAPD (ranging from 3.5 to 12.3) and BD (ranging from 1.8 to 8.5).
  • The risk for NAPD and BD was also elevated in unaffected siblings of individuals with ASD (ORs 1.8 and 1.7, respectively).
  • Risks were higher when ASD was diagnosed before age 28 compared to before age 16, and varied based on intellectual disability status.

Conclusions:

  • Autism spectrum disorder is associated with a significantly elevated risk of developing nonaffective psychotic disorder and bipolar disorder.
  • These findings highlight the importance of monitoring for these conditions in individuals with ASD and their families.
  • The results have implications for clinical management and understanding the complex etiology of these disorders.
Abstract

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