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Machine learning nominates the inositol pathway and novel genes in Parkinson's disease.
Yu, Eric; Larivière, Roxanne; Thomas, Rhalena A; Liu, Lang; Senkevich, Konstantin; Rahayel, Shady; Trempe, Jean-François; Fon, Edward A; Gan-Or, Ziv.
Afiliação
  • Yu E; Department of Human Genetics, McGill University, Montreal, Quebec H3A 0G4, Canada.
  • Larivière R; The Neuro (Montreal Neurological Institute-Hospital), Montreal, Quebec H3A 2B4, Canada.
  • Thomas RA; Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec H3A 0G4, Canada.
  • Liu L; Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec H3A 0G4, Canada.
  • Senkevich K; Early Drug Discovery Unit (EDDU), Montreal Neurological Institute-Hospital (The Neuro), Montreal, Quebec H3A 2B4, Canada.
  • Rahayel S; Department of Human Genetics, McGill University, Montreal, Quebec H3A 0G4, Canada.
  • Trempe JF; The Neuro (Montreal Neurological Institute-Hospital), Montreal, Quebec H3A 2B4, Canada.
  • Fon EA; The Neuro (Montreal Neurological Institute-Hospital), Montreal, Quebec H3A 2B4, Canada.
  • Gan-Or Z; Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec H3A 0G4, Canada.
Brain ; 147(3): 887-899, 2024 03 01.
Article em En | MEDLINE | ID: mdl-37804111
ABSTRACT
There are 78 loci associated with Parkinson's disease in the most recent genome-wide association study (GWAS), yet the specific genes driving these associations are mostly unknown. Herein, we aimed to nominate the top candidate gene from each Parkinson's disease locus and identify variants and pathways potentially involved in Parkinson's disease. We trained a machine learning model to predict Parkinson's disease-associated genes from GWAS loci using genomic, transcriptomic and epigenomic data from brain tissues and dopaminergic neurons. We nominated candidate genes in each locus and identified novel pathways potentially involved in Parkinson's disease, such as the inositol phosphate biosynthetic pathway (INPP5F, IP6K2, ITPKB and PPIP5K2). Specific common coding variants in SPNS1 and MLX may be involved in Parkinson's disease, and burden tests of rare variants further support that CNIP3, LSM7, NUCKS1 and the polyol/inositol phosphate biosynthetic pathway are associated with the disease. Functional studies are needed to further analyse the involvements of these genes and pathways in Parkinson's disease.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Estudo de Associação Genômica Ampla Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Brain Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Estudo de Associação Genômica Ampla Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Brain Ano de publicação: 2024 Tipo de documento: Article