Your browser doesn't support javascript.
loading
Identification of brain cell types underlying genetic association with word reading and correlated traits.
Price, Kaitlyn M; Wigg, Karen G; Nigam, Anukrati; Feng, Yu; Blokland, Kirsten; Wilkinson, Margaret; Kerr, Elizabeth N; Guger, Sharon L; Lovett, Maureen W; Strug, Lisa J; Tripathy, Shreejoy J; Barr, Cathy L.
Afiliação
  • Price KM; Division of Experimental and Translational Neuroscience, Krembil Research Institute, University Health Network, Toronto, ON, Canada.
  • Wigg KG; Program in Neuroscience and Mental Health, Hospital for Sick Children, Toronto, ON, Canada.
  • Nigam A; Department of Physiology, University of Toronto, Toronto, ON, Canada.
  • Feng Y; Division of Experimental and Translational Neuroscience, Krembil Research Institute, University Health Network, Toronto, ON, Canada.
  • Blokland K; Krembil Centre for Neuroinformatics, Centre for Addiction and Mental Health, Toronto, ON, Canada.
  • Wilkinson M; Institute of Medical Science, University of Toronto, Toronto, ON, Canada.
  • Kerr EN; Division of Experimental and Translational Neuroscience, Krembil Research Institute, University Health Network, Toronto, ON, Canada.
  • Guger SL; Program in Neuroscience and Mental Health, Hospital for Sick Children, Toronto, ON, Canada.
  • Lovett MW; Program in Neuroscience and Mental Health, Hospital for Sick Children, Toronto, ON, Canada.
  • Strug LJ; Department of Psychology, Hospital for Sick Children, Toronto, ON, Canada.
  • Tripathy SJ; Department of Pediatrics, University of Toronto, Toronto, ON, Canada.
  • Barr CL; Department of Psychology, Hospital for Sick Children, Toronto, ON, Canada.
Mol Psychiatry ; 28(4): 1719-1730, 2023 04.
Article em En | MEDLINE | ID: mdl-36750735
ABSTRACT
Neuroimaging studies implicate multiple cortical regions in reading ability/disability. However, the neural cell types integral to the reading process are unknown. To contribute to this gap in knowledge, we integrated genetic results from genome-wide association studies for word reading (n = 5054) with gene expression datasets from adult/fetal human brain. Linkage disequilibrium score regression (LDSC) suggested that variants associated with word reading were enriched in genes expressed in adult excitatory neurons, specifically layer 5 and 6 FEZF2 expressing neurons and intratelencephalic (IT) neurons, which express the marker genes LINC00507, THEMIS, or RORB. Inhibitory neurons (VIP, SST, and PVALB) were also found. This finding was interesting as neurometabolite studies previously implicated excitatory-inhibitory imbalances in the etiology of reading disabilities (RD). We also tested traits that shared genetic etiology with word reading (previously determined by polygenic risk scores) attention-deficit/hyperactivity disorder (ADHD), educational attainment, and cognitive ability. For ADHD, we identified enrichment in L4 IT adult excitatory neurons. For educational attainment and cognitive ability, we confirmed previous studies identifying multiple subclasses of adult cortical excitatory and inhibitory neurons, as well as astrocytes and oligodendrocytes. For educational attainment and cognitive ability, we also identified enrichment in multiple fetal cortical excitatory and inhibitory neurons, intermediate progenitor cells, and radial glial cells. In summary, this study supports a role of excitatory and inhibitory neurons in reading and excitatory neurons in ADHD and contributes new information on fetal cell types enriched in educational attainment and cognitive ability, thereby improving our understanding of the neurobiological basis of reading/correlated traits.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno do Deficit de Atenção com Hiperatividade / Dislexia Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans Idioma: En Revista: Mol Psychiatry Assunto da revista: BIOLOGIA MOLECULAR / PSIQUIATRIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno do Deficit de Atenção com Hiperatividade / Dislexia Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans Idioma: En Revista: Mol Psychiatry Assunto da revista: BIOLOGIA MOLECULAR / PSIQUIATRIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Canadá