Autism spectrum disorder polygenic scores are associated with every day executive function in children admitted for clinical assessment.
Tonje Torske, Terje Naerland, Francesco Bettella and 6 others
PMID 31571410WHAT IT FOUND
Children and adolescents referred for autism assessment with higher genetic risk for autism had more parent-reported everyday problems with behavior regulation.
The genetic risk was not linked to other executive function or social difficulty scores.
Key findings
01In the clinical sample, the highest autism genetic risk score group had a mean behavior regulation t-score of 71.5, compared with 62.9 in the lowest group (P = 0.015).
02There was no significant difference in metacognition t-scores between the lowest and highest autism genetic risk score groups.
03After controlling for age, sex, IQ, social difficulty score, and genetic principal components, only social difficulty score, sex, and autism genetic risk group contributed significantly to behavior regulation scores; ADHD and intelligence genetic risk groups did not.
STILL TO COME
How it was doneWhat they foundWhat it means for OTs
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What it does not show
The study measured associations at one time point, so it cannot show that genetic risk caused executive function problems. The authors state that autism genetic risk scores are not yet accurate enough for clinical diagnosis or treatment planning. The significant finding depended on splitting participants into extreme low and high genetic risk groups; the association disappeared when genetic risk was analyzed as a continuous score. P-values were not adjusted for multiple testing, and several executive function outcomes were examined. The sample was moderate in size, mostly boys, and included children referred for autism assessment rather than a community sample. Children with IQ below 70 and significant sensory losses were excluded, so the findings may not apply to more impaired children. Executive function was measured only by parent report, and parent-report executive function scores correlate poorly with performance-based tests. ADHD was recorded only as a clinical diagnosis, without symptom-level measures, which may blur differences between autism and ADHD genetic risk. The genetic ancestry was European and the sample was Norwegian, so findings may not generalize.
Declared interests
No author conflict-of-interest or funding statement is included in the supplied text. The article is tagged as research supported by non-U.S. government.
The easy way to misread this
Do not treat a high autism genetic risk score as a clinical test or as proof that genes caused a child's behavior regulation problems. The score was not clinically usable, the study measured associations at one time point, and the effect was limited to one parent-report executive function score.