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Evaluating Computerised Assessment of Motor Imitation (CAMI) for identifying autism-specific difficulties not observed for attention-deficit hyperactivity disorder or neurotypical development

Abstract:
Background: Reliable and specific biomarkers that can distinguish autism spectrum disorders (ASDs) from commonly co-occurring attention-deficit/hyperactivity disorder (ADHD) are lacking, causing misses and delays in diagnosis, and reducing access to interventions and quality of life. Aims: To examine whether an innovative, brief (1-min), videogame method called Computerised Assessment of Motor Imitation (CAMI), can identify ASD-specific imitation differences compared with neurotypical children and children with ADHD. Method: This cross-sectional study used CAMI alongside standardised parent-report (Social Responsiveness Scale, Second Edition) and observational measures of autism (Autism Diagnostic Observation Schedule-Second Edition; ADOS-2), ADHD (Conners) and motor ability (Physical and Neurological Examination for Soft Signs). The sample comprised 183 children aged 7–13 years, with ADHD (without ASD), with ASD (with and without ADHD) and who were neurotypical. Results: Regardless of co-occurring ADHD, children with ASD showed poorer CAMI performance than neurotypical children (P < 0.0001; adjusted R2 = 0.28), whereas children with ADHD and neurotypical children showed similar CAMI performance. Receiver operating curve and support vector machine analyses showed that CAMI distinguishes ASD from both neurotypical children (80% true positive rate) and children with ADHD (70% true positive rate), with a high success rate significantly above chance. Among children with ASD, poor CAMI performance was associated with increased autism traits, particularly ADOS-2 measures of social affect and restricted and repetitive behaviours (adjusted R2 = 0.23), but not with ADHD traits or motor ability. Conclusions: Four levels of analyses confirm that poor imitation measured by the low-cost and scalable CAMI method specifically distinguishes ASD not only from neurotypical development, but also from commonly co-occurring ADHD.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1192/bjp.2024.235

Authors


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Funder identifier:
https://ror.org/021nxhr62
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Funder identifier:
https://ror.org/01cwqze88


Publisher:
Cambridge University Press
Journal:
The British Journal of Psychiatry More from this journal
Volume:
228
Issue:
1
Pages:
29-36
Publication date:
2025-01-28
Acceptance date:
2024-10-09
DOI:
EISSN:
1472-1465
ISSN:
0007-1250


Language:
English
Keywords:
Pubs id:
2360036
UUID:
uuid_d38ac075-beeb-4bfb-914b-655c706c071b
Local pid:
pubs:2360036
Source identifiers:
3571554
Deposit date:
2025-12-17
ARK identifier:
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