La Trobe

Toward better characterization of restricted and repetitive behaviors in individuals with germline heterozygous PTEN mutations

Download (1013.98 kB)
journal contribution
posted on 2025-12-16, 05:44 authored by Mirko UljarevicMirko Uljarevic, TW Frazier, G Rached, RM Busch, P Klaas, S Srivastava, JA Martinez-Agosto, M Sahin, C Eng, AY Hardan
<p dir="ltr">This study aimed to further our understanding of restricted and repetitive behaviors (RRB) among individuals with germline pathogenic mutations in PTEN by providing multimethod characterization and comparison of key RRB subdomains across individuals with PTEN mutations with autism spectrum disorder (ASD) (PTEN-ASD), with PTEN mutations without ASD (PTEN-No ASD) and with ASD and macrocephaly but without PTEN mutations (Macro-ASD). </p><p dir="ltr">Of 86 total research participants, 38 had PTEN-ASD (Mage = 8.93 years, SDage = 4.75), 25 Macro-ASD (Mage = 11.99 years; SDage = 5.15), and 23 PTEN-No ASD (Mage = 8.94 years; SDage = 4.85). The Repetitive Behavior Scale-Revised (RBS-R) and the Autism Diagnostic Interview-Revised (ADI-R) were used as measures of distinct RRB domains. </p><p dir="ltr">There were significant group differences in the RBS-R repetitive motor behaviors (RMB; F = 4.52, p = 0.014, ω<sup>2</sup> = 0.08), insistence on sameness (IS; F = 4.11, p = 0.02, ω<sup>2</sup> = 0.05), and circumscribed interests (CI; F = 7.80, p = 0.001, ω<sup>2</sup> = 0.14) scales. Post hoc comparisons showed that the PTEN-No ASD group had significantly lower RMB, IS, and CI scores compared to both PTEN-ASD and Macro-ASD groups. Importantly, PTEN-No ASD group still showed elevated RRB levels. Furthermore, there was a portion of individuals in PTEN-No ASD group whose Full-Scale Intelligence Quotient (FSIQ) was >70 that did not show floor level scores in the RMB domain. </p><p dir="ltr">After adjusting for age and FSIQ scores, group differences were no longer statistically significant. RMB, IS, and CI domains showed distinct association patterns with sex, age, and FSIQ. This investigation provides the largest and most comprehensive characterization of distinct RRB domains in individuals with PTEN mutations to date. Despite the limitations, our findings have important assessment and treatment implications.</p>

Funding

Australian Research Council Discovery Early Career Researcher Award. Grant Number: DE180100632

This study was funded, in part, by the National Institute of Health Developmental Synaptopathies Consortium (U54NS092090; PI/Network Director: Sahin; Project 2 Leaders/PIs: Eng & Busch) and the Ambrose Monell Foundation (to Charis Eng). The Developmental Synaptopathies Consortium (U54NS092090) is part of the National Center for Advancing Translational Sciences (NCATS) Rare Diseases Clinical Research Network (RDCRN) and is supported by the RDCRN Data Management and Coordinating Center (DMCC) (U2CTR002818). RDCRN is an initiative of the Office of Rare Diseases Research (ORDR), NCATS, funded through a collaboration between NCATS and the National Institute of Neurological Disorders and Stroke of the National Institutes of Health (NINDS), Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD) and National Institute of Mental Health (NIMH).

History

Publication Date

2021-11-01

Journal

American Journal of Medical Genetics Part A

Volume

185

Issue

11

Pagination

10p. (p. 3401-3410)

Publisher

Wiley

ISSN

1552-4825

Rights Statement

© 2021 Wiley Periodicals LLC This is the peer reviewed version of the following article: Uljarević M, et al (2021). Toward better characterization of restricted and repetitive behaviors in individuals with germline heterozygous PTEN mutations. American Journal of Medical Genetics, Part A, 185(11), 3401-3410, which has been published in final form at http://doi.org/10.1002/ajmg.a.62458. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.

Usage metrics

    Journal Articles

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC