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Autism spectrum disorder and brain volume link through a set of mTOR-related genes.
Arenella, Martina; Mota, Nina R; Teunissen, Mariel W A; Brunner, Han G; Bralten, Janita.
Afiliación
  • Arenella M; Department of Human Genetics, Radboud university medical center, Nijmegen, The Netherlands.
  • Mota NR; Department of Forensic and Neurodevelopmental Science, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
  • Teunissen MWA; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands.
  • Brunner HG; Department of Human Genetics, Radboud university medical center, Nijmegen, The Netherlands.
  • Bralten J; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands.
J Child Psychol Psychiatry ; 64(7): 1007-1014, 2023 07.
Article en En | MEDLINE | ID: mdl-36922714
ABSTRACT

BACKGROUND:

Larger than average head and brain sizes are often observed in individuals with autism spectrum disorders (ASDs). ASD and brain volume are both highly heritable, with multiple genetic variants contributing. However, it is unclear whether ASD and brain volume share any genetic mechanisms. Genes from the mammalian target of rapamycin (mTOR) pathway influence brain volume, and variants are found in rare genetic syndromes that include ASD features. Here we investigated whether variants in mTOR-related genes are also associated with ASD and if they constitute a genetic link between large brains and ASD.

METHODS:

We extended our analyses between large heads (macrocephaly) and rare de novo mTOR-related variants in an intellectual disability cohort (N = 2,258). Subsequently using Fisher's exact tests we investigated the co-occurrence of mTOR-related de novo variants and ASD in the de-novo-db database (N = 23,098). We next selected common genetic variants within a set of 96 mTOR-related genes in genome-wide genetic association data of ASD (N = 46,350) to test gene-set association using MAGMA. Lastly, we tested genetic correlation between genome-wide genetic association data of ASD (N = 46,350) and intracranial volume (N = 25,974) globally using linkage disequilibrium score regression as well as mTOR specific by restricting the genetic correlation to the mTOR-related genes using GNOVA.

RESULTS:

Our results show that both macrocephaly and ASD occur above chance level in individuals carrying rare de novo variants in mTOR-related genes. We found a significant mTOR gene-set association with ASD (p = .0029) and an mTOR-stratified positive genetic correlation between ASD and intracranial volume (p = .027), despite the absence of a significant genome-wide correlation (p = .81).

CONCLUSIONS:

This work indicates that both rare and common variants in mTOR-related genes are associated with brain volume and ASD and genetically correlate them in the expected direction. We demonstrate that genes involved in mTOR signalling are potential mediators of the relationship between having a large brain and having ASD.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastorno del Espectro Autista / Discapacidad Intelectual Límite: Humans Idioma: En Revista: J Child Psychol Psychiatry Año: 2023 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastorno del Espectro Autista / Discapacidad Intelectual Límite: Humans Idioma: En Revista: J Child Psychol Psychiatry Año: 2023 Tipo del documento: Article País de afiliación: Países Bajos
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