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Discordant associations of educational attainment with ASD and ADHD implicate a polygenic form of pleiotropy.
Verhoef, Ellen; Grove, Jakob; Shapland, Chin Yang; Demontis, Ditte; Burgess, Stephen; Rai, Dheeraj; Børglum, Anders D; St Pourcain, Beate.
Afiliación
  • Verhoef E; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.
  • Grove J; International Max Planck Research School for Language Sciences, Nijmegen, The Netherlands.
  • Shapland CY; The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Aarhus, Denmark.
  • Demontis D; Department of Biomedicine (Human Genetics) and Centre for Integrative Sequencing, iSEQ, Aarhus University, Aarhus, Denmark.
  • Burgess S; Center for Genomics and Personalized Medicine, Aarhus, Denmark.
  • Rai D; Bioinformatics Research Centre, Aarhus University, Aarhus, Denmark.
  • Børglum AD; MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
  • St Pourcain B; Population Health Sciences, University of Bristol, Bristol, UK.
Nat Commun ; 12(1): 6534, 2021 11 11.
Article en En | MEDLINE | ID: mdl-34764245
ABSTRACT
Autism Spectrum Disorder (ASD) and Attention-Deficit/Hyperactivity Disorder (ADHD) are complex co-occurring neurodevelopmental conditions. Their genetic architectures reveal striking similarities but also differences, including strong, discordant polygenic associations with educational attainment (EA). To study genetic mechanisms that present as ASD-related positive and ADHD-related negative genetic correlations with EA, we carry out multivariable regression analyses using genome-wide summary statistics (N = 10,610-766,345). Our results show that EA-related genetic variation is shared across ASD and ADHD architectures, involving identical marker alleles. However, the polygenic association profile with EA, across shared marker alleles, is discordant for ASD versus ADHD risk, indicating independent effects. At the single-variant level, our results suggest either biological pleiotropy or co-localisation of different risk variants, implicating MIR19A/19B microRNA mechanisms. At the polygenic level, they point to a polygenic form of pleiotropy that contributes to the detectable genome-wide correlation between ASD and ADHD and is consistent with effect cancellation across EA-related regions.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastorno por Déficit de Atención con Hiperactividad / Trastorno del Espectro Autista Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2021 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastorno por Déficit de Atención con Hiperactividad / Trastorno del Espectro Autista Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2021 Tipo del documento: Article País de afiliación: Países Bajos
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