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Published on: December 7, 2018
Autism spectrum disorders: a meta-analysis of executive function
E A Demetriou1, A Lampit2, D S Quintana1,3
1Autism Clinic for Translational Research, Brain and Mind Centre, Central Clinical School, Faculty of Medicine, University of Sydney, Camperdown, Sydney, NSW, Australia.
This meta-analysis confirms broad executive dysfunction in autism spectrum disorder (ASD) across development. Findings suggest current measures lack diagnostic sensitivity, highlighting a need for improved tools.
Area of Science:
- Neuroscience
- Psychology
- Developmental Psychology
Background:
- Evidence regarding executive dysfunction (EF) in autism spectrum disorders (ASD) is inconsistent.
- Understanding EF's role is crucial for effective ASD diagnosis and intervention strategies.
Purpose of the Study:
- To meta-analyze EF performance in ASD, examining subdomain fractionation, clinical utility of measures, and moderator influences (age, gender, diagnosis).
- To assess the clinical sensitivity of EF measures for ASD diagnosis and treatment.
Main Methods:
- Searched Embase, Medline, and PsychINFO for peer-reviewed studies (1980-June 2016) comparing EF in ASD with neurotypical controls.
- Utilized a random-effects model with subgroup analysis for moderators. Primary outcome: Hedges' g effect size. Clinical sensitivity: overlap percentage (OL%).
- Followed PRISMA guidelines for reporting. Included 235 studies with 14,081 participants (6,816 ASD, 7,265 controls).
Main Results:
- A moderate overall effect size (Hedges' g=0.48) for reduced EF in ASD was observed, consistent across domains.
- Most moderator comparisons were non-significant; EF dysfunction effect size decreased post-DSM-III introduction.
- Few EF measures demonstrated clinical sensitivity; fractionation of EF into subdomains was not supported.
Conclusions:
- Confirms broad, development-stable executive dysfunction in ASD.
- Current EF measures lack diagnostic sensitivity and do not effectively fractionate into specific subdomains.
- Prioritizes development of feasible EF measures with enhanced clinical sensitivity for ASD diagnosis and treatment.
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