Look duration at the face as a developmental endophenotype: elucidating pathways to autism and ADHD

Identifying developmental endophenotypes on the pathway between genetics and behavior is critical to uncovering the mechanisms underlying neurodevelopmental conditions. In this proof-of-principle study, we explored whether early disruptions in visual attention are a unique or shared candidate endoph...

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Veröffentlicht in:Development and psychopathology 2020-10, Vol.32 (4), p.1303-1322
Hauptverfasser: Gui, Anna, Mason, Luke, Gliga, Teodora, Hendry, Alexandra, Begum Ali, Jannath, Pasco, Greg, Shephard, Elizabeth, Curtis, Charles, Charman, Tony, Johnson, Mark H., Meaburn, Emma, Jones, Emily J. H.
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container_end_page 1322
container_issue 4
container_start_page 1303
container_title Development and psychopathology
container_volume 32
creator Gui, Anna
Mason, Luke
Gliga, Teodora
Hendry, Alexandra
Begum Ali, Jannath
Pasco, Greg
Shephard, Elizabeth
Curtis, Charles
Charman, Tony
Johnson, Mark H.
Meaburn, Emma
Jones, Emily J. H.
description Identifying developmental endophenotypes on the pathway between genetics and behavior is critical to uncovering the mechanisms underlying neurodevelopmental conditions. In this proof-of-principle study, we explored whether early disruptions in visual attention are a unique or shared candidate endophenotype of autism spectrum disorder (ASD) and attention-deficit/hyperactivity disorder (ADHD). We calculated the duration of the longest look (i.e., peak look) to faces in an array-based eye-tracking task for 335 14-month-old infants with and without first-degree relatives with ASD and/or ADHD. We leveraged parent-report and genotype data available for a proportion of these infants to evaluate the relation of looking behavior to familial (n = 285) and genetic liability (using polygenic scores, n = 185) as well as ASD and ADHD-relevant temperament traits at 2 years of age (shyness and inhibitory control, respectively, n = 272) and ASD and ADHD clinical traits at 6 years of age (n = 94). Results showed that longer peak looks at the face were associated with elevated polygenic scores for ADHD (β = 0.078, p = .023), but not ASD (β = 0.002, p = .944), and with elevated ADHD traits in mid-childhood (F(1,88) = 6.401, p = .013, $\eta _p^2$=0.068; ASD: F (1,88) = 3.218, p = .076), but not in toddlerhood (ps > 0.2). This pattern of results did not emerge when considering mean peak look duration across face and nonface stimuli. Thus, alterations in attention to faces during spontaneous visual exploration may be more consistent with a developmental endophenotype of ADHD than ASD. Our work shows that dissecting paths to neurodevelopmental conditions requires longitudinal data incorporating polygenic contribution, early neurocognitive function, and clinical phenotypic variation.
doi_str_mv 10.1017/S0954579420000930
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subjects Age
Attention Deficit Disorder with Hyperactivity - genetics
Attention deficit hyperactivity disorder
Autism
Autism Spectrum Disorder - genetics
Autistic Disorder
Child
Child, Preschool
Children
Cognition
Consortia
Endophenotypes
Face
Genotypes
Humans
Hyperactivity
Infant
Infants
Phenotypic variations
Polygenic inheritance
Psychiatry
Psychopathology
Special Section Articles
Temperament
Visual perception
title Look duration at the face as a developmental endophenotype: elucidating pathways to autism and ADHD
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