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April 18, 2026BJPsych Open0 citationsOpen Access

Childhood ADHD and autism spectrum disorder difficulties: exploring the impact of copy number variants on young adult outcomes

CDCharlotte DennisonCardiff UniversityMFMia FlanaganCardiff UniversityASAmy ShakeshaftCardiff University

Key Points

  • This research aims to examine whether copy number variants (CNVs) influence adult outcomes in individuals with ADHD or autism spectrum disorder (ASD).
  • Utilized data from the Avon Longitudinal Study of Parents and Children in the UK.
  • Defined ADHD and ASD difficulties categorically from ages 7 to 16.
  • Assessed various adulthood outcomes like education attainment and mental health at ages 18, 24, and 25.
  • Applied logistic regressions to explore the relationship between CNVs and adult outcomes.
  • Employed multiple imputation to handle missing data in the analyses.
  • Found no strong evidence that CNVs moderate the effects of ADHD or ASD on young adult outcomes.
  • Confidence intervals for the moderating effect were wide, indicating inconclusive results for CNVs.

Abstract

Rare copy number variants (CNVs; deleted/duplicated DNA segments) are associated with childhood attention-deficit hyperactivity disorder (ADHD) and autism spectrum disorder (ASD). It is unknown whether carrying a CNV moderates the effect of ADHD/ASD on adult outcomes. In a UK population-based cohort, the Avon Longitudinal Study of Parents and Children, ADHD and ASD difficulties at ages 7-16 years were defined categorically. Outcomes included: General Certificate of Secondary Education non-attainment; depression at ages 18 and 24; functioning at age 25; not in education, employment or training; and receiving state benefits at age 25. Logistic regressions were used to assess associations between ADHD/ASD and outcomes, and to test CNVs as moderators. Multiple imputation was used to account for data missingness. We did not find strong evidence of CNVs moderating the effect of ADHD or ASD on young adult outcomes. However, confidence intervals for the moderating effect were wide, so further research in larger clinical samples is necessary.

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Cite This Study

Dennison et al. (2026) studied this question.

synapsesocial.com/papers/69e3201440886becb653f31ahttps://doi.org/10.1192/bjo.2026.11018
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1The Role of Rare Copy Number Variants in the Functional Outcomes of Individuals With Neurodevelopmental Conditions2024
  2. 2Exploring Copy Number Variants in a Cohort of Children Affected by ADHD: Clinical Investigation and Translational Insights2025
  3. 3The copy number variant architecture of psychopathology and cognitive development in the ABCD study2024 · 1 citations
  4. 4Contribution of Copy Number Variants and Cumulative Genetic Load to Autism Spectrum Disorders: Integrative Insights from Chromosomal Microarray Analysis2026
  5. 5Population-Based Risk of Psychiatric Disorders Associated With Recurrent Copy Number Variants2024 · 14 citations