Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

A genetics-first approach to dissecting the heterogeneity of autism: phenotypic comparison of autism risk copy number variants

Chawner, Samuel, Doherty, Joanne L., Anney, Richard, Antshel, Kevin M., Bearden, Carrie E., Bernier, Raphael, Chung, Wendy K., Clements, Caitlin C., Curran, Sarah R., Cuturilo, Goran, Fiksinski, Ania M., Gallagher, Louise, Goin-Koche, Robin P., Kushan, Leila, Gur, Raquel E., Hanson, Ellen, Jacquemont, Sebastien, Kates, Wendy R., Maillard, Anne M., McDonald-McGinn, Donna M., MihaljevicMihaljevic, Marina Mihaljevic, Miller, Judith S., Moss, Hayley, Pejovic-Milovancevic, Milica, Schultz, Robert T., Green-Snyder, LeeAnne, Vorstman, Jacob A., Wenger, Tara L., Hall, Jeremy, Owen, Michael J. and van den Bree, Marianne B.M. 2021. A genetics-first approach to dissecting the heterogeneity of autism: phenotypic comparison of autism risk copy number variants. American Journal of Psychiatry 178 (1) , pp. 77-86. 10.1176/appi.ajp.2020.20010015
Item availability restricted.

[img] PDF - Accepted Post-Print Version
Restricted to Repository staff only until 1 January 2022 due to copyright restrictions.

Download (291kB)
[img] PDF (Figures) - Supplemental Material
Restricted to Repository staff only until 1 January 2022 due to copyright restrictions.

Download (158kB)
[img] PDF (Tables) - Supplemental Material
Restricted to Repository staff only until 1 January 2022 due to copyright restrictions.

Download (212kB)

Abstract

Objective: Certain copy number variants (CNVs) greatly increase the risk of autism. The authors conducted a genetics-first study to investigate whether heterogeneity in the clinical presentation of autism is underpinned by specific genotype-phenotype relationships. Methods: This international study included 547 individuals (mean age, 12.3 years [SD=4.2], 54% male) who were ascertained on the basis of having a genetic diagnosis of a rare CNV associated with high risk of autism (82 16p11.2 deletion carriers, 50 16p11.2 duplication carriers, 370 22q11.2 deletion carriers, and 45 22q11.2 duplication carriers), as well as 2,027 individuals (mean age, 9.1 years [SD=4.9], 86% male) with autism of heterogeneous etiology. Assessments included the Autism Diagnostic Interview-Revised and IQ testing. Results: The four genetic variant groups differed in autism symptom severity, autism subdomain profile, and IQ profile. However, substantial variability was observed in phenotypic outcome in individual genetic variant groups (74%-97% of the variance, depending on the trait), whereas variability between groups was low (1%-21%, depending on the trait). CNV carriers who met autism criteria were compared with individuals with heterogeneous autism, and a range of profile differences were identified. When clinical cutoff scores were applied, 54% of individuals with one of the four CNVs who did not meet full autism diagnostic criteria had elevated levels of autistic traits. Conclusions: Many CNV carriers do not meet full diagnostic criteria for autism but nevertheless meet clinical cutoffs for autistic traits. Although profile differences between variants were observed, there is considerable variability in clinical symptoms in the same variant.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Psychology
Publisher: American Psychiatric Publishing
ISSN: 0002-953X
Date of First Compliant Deposit: 25 August 2020
Date of Acceptance: 24 August 2020
Last Modified: 16 Feb 2021 11:56
URI: http://orca.cardiff.ac.uk/id/eprint/134372

Actions (repository staff only)

Edit Item Edit Item