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Genome-wide association and multi-omics studies identify MGMT as a novel risk gene for Alzheimer's disease among women.
Chung, Jaeyoon; Das, Anjali; Sun, Xinyu; Sobreira, Débora R; Leung, Yuk Yee; Igartua, Catherine; Mozaffari, Sahar; Chou, Yi-Fan; Thiagalingam, Sam; Mez, Jesse; Zhang, Xiaoling; Jun, Gyungah R; Stein, Thor D; Kunkle, Brian W; Martin, Eden R; Pericak-Vance, Margaret A; Mayeux, Richard; Haines, Jonathan L; Schellenberg, Gerard D; Nobrega, Marcelo A; Lunetta, Kathryn L; Pinto, Jayant M; Wang, Li-San; Ober, Carole; Farrer, Lindsay A.
Afiliação
  • Chung J; Department of Medicine (Biomedical Genetics), Boston University School of Medicine, Boston, Massachusetts, USA.
  • Das A; Department of Human Genetics, The University of Chicago, Chicago, Illinois, USA.
  • Sun X; Department of Medicine (Biomedical Genetics), Boston University School of Medicine, Boston, Massachusetts, USA.
  • Sobreira DR; Department of Surgery/Section of Otolaryngology-Head and Neck Surgery, The University of Chicago, Chicago, Illinois, USA.
  • Leung YY; Penn Neurodegeneration Genomics Center, Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
  • Igartua C; Department of Human Genetics, The University of Chicago, Chicago, Illinois, USA.
  • Mozaffari S; Department of Human Genetics, The University of Chicago, Chicago, Illinois, USA.
  • Chou YF; Penn Neurodegeneration Genomics Center, Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
  • Thiagalingam S; Department of Medicine (Biomedical Genetics), Boston University School of Medicine, Boston, Massachusetts, USA.
  • Mez J; Department of Neurology, Boston University School of Medicine, Boston, Massachusetts, USA.
  • Zhang X; Department of Medicine (Biomedical Genetics), Boston University School of Medicine, Boston, Massachusetts, USA.
  • Jun GR; Department of Medicine (Biomedical Genetics), Boston University School of Medicine, Boston, Massachusetts, USA.
  • Stein TD; Department of Ophthalmology, Boston University School of Medicine, Boston, Massachusetts, USA.
  • Kunkle BW; Department of Biostatistics, Boston University School of Public Health, Boston, Massachusetts, USA.
  • Martin ER; Department of Pathology & Laboratory Medicine, Boston University School of Medicine, Boston, Massachusetts, USA.
  • Pericak-Vance MA; Dr. John T. Macdonald Foundation of Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida, USA.
  • Mayeux R; Dr. John T. Macdonald Foundation of Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida, USA.
  • Haines JL; Dr. John T. Macdonald Foundation of Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida, USA.
  • Schellenberg GD; Department of Neurology, Columbia University, New York City, New York, USA.
  • Nobrega MA; Department of Population and Quantitative Health Sciences and Cleveland Institute for Computational Biology, Case Western Reserve University, Cleveland, Ohio, USA.
  • Lunetta KL; Penn Neurodegeneration Genomics Center, Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
  • Pinto JM; Department of Human Genetics, The University of Chicago, Chicago, Illinois, USA.
  • Wang LS; Department of Biostatistics, Boston University School of Public Health, Boston, Massachusetts, USA.
  • Ober C; Department of Surgery/Section of Otolaryngology-Head and Neck Surgery, The University of Chicago, Chicago, Illinois, USA.
  • Farrer LA; Penn Neurodegeneration Genomics Center, Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
Alzheimers Dement ; 2022 Jun 30.
Article em En | MEDLINE | ID: mdl-35770850
INTRODUCTION: Variants in the tau gene (MAPT) region are associated with breast cancer in women and Alzheimer's disease (AD) among persons lacking apolipoprotein E ε4 (ε4-). METHODS: To identify novel genes associated with tau-related pathology, we conducted two genome-wide association studies (GWAS) for AD, one among 10,340 ε4- women in the Alzheimer's Disease Genetics Consortium (ADGC) and another in 31 members (22 women) of a consanguineous Hutterite kindred. RESULTS: We identified novel associations of AD with MGMT variants in the ADGC (rs12775171, odds ratio [OR] = 1.4, P = 4.9 × 10-8 ) and Hutterite (rs12256016 and rs2803456, OR = 2.0, P = 1.9 × 10-14 ) datasets. Multi-omics analyses showed that the most significant and largest number of associations among the single nucleotide polymorphisms (SNPs), DNA-methylated CpGs, MGMT expression, and AD-related neuropathological traits were observed among women. Furthermore, promoter capture Hi-C analyses revealed long-range interactions of the MGMT promoter with MGMT SNPs and CpG sites. DISCUSSION: These findings suggest that epigenetically regulated MGMT expression is involved in AD pathogenesis, especially in women.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article