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Sex differences in the genetic predictors of Alzheimer's pathology.
Dumitrescu, Logan; Barnes, Lisa L; Thambisetty, Madhav; Beecham, Gary; Kunkle, Brian; Bush, William S; Gifford, Katherine A; Chibnik, Lori B; Mukherjee, Shubhabrata; De Jager, Philip L; Kukull, Walter; Crane, Paul K; Resnick, Susan M; Keene, C Dirk; Montine, Thomas J; Schellenberg, Gerard D; Deming, Yuetiva; Chao, Michael J; Huentelman, Matt; Martin, Eden R; Hamilton-Nelson, Kara; Shaw, Leslie M; Trojanowski, John Q; Peskind, Elaine R; Cruchaga, Carlos; Pericak-Vance, Margaret A; Goate, Alison M; Cox, Nancy J; Haines, Jonathan L; Zetterberg, Henrik; Blennow, Kaj; Larson, Eric B; Johnson, Sterling C; Albert, Marilyn; Bennett, David A; Schneider, Julie A; Jefferson, Angela L; Hohman, Timothy J.
Afiliação
  • Dumitrescu L; Vanderbilt Memory and Alzheimer's Center, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Barnes LL; Vanderbilt Genetics Institute, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Thambisetty M; Rush Alzheimer's Disease Center, Rush University Medical Center, Chicago, IL, USA.
  • Beecham G; Laboratory of Behavioral Neuroscience, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.
  • Kunkle B; John T MacDonald Foundation Department of Human Genetics, University of Miami, Miami, FL, USA.
  • Bush WS; John P. Hussman Institute for Human Genomics, University of Miami School of Medicine, Miami, FL, USA.
  • Gifford KA; John P. Hussman Institute for Human Genomics, University of Miami School of Medicine, Miami, FL, USA.
  • Chibnik LB; Department of Population and Quantitative Health Sciences, Institute for Computational Biology, Case Western Reserve University, Cleveland, OH, USA.
  • Mukherjee S; Vanderbilt Memory and Alzheimer's Center, Vanderbilt University Medical Center, Nashville, TN, USA.
  • De Jager PL; Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
  • Kukull W; Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • Crane PK; Department of Medicine, University of Washington, Seattle, WA, USA.
  • Resnick SM; Center for Translational and Computational Neuroimmunology, Department of Neurology, Columbia University Medical Center, New York, NY, USA.
  • Keene CD; Cell Circuits Program, Broad Institute, Cambridge MA, USA.
  • Montine TJ; Department of Epidemiology, School of Public Health, University of Washington, Seattle, WA, USA.
  • Schellenberg GD; Department of Medicine, University of Washington, Seattle, WA, USA.
  • Deming Y; Laboratory of Behavioral Neuroscience, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.
  • Chao MJ; Department of Pathology, University of Washington, Seattle, WA, USA.
  • Huentelman M; Department of Pathology, Stanford University, Stanford, CA, USA.
  • Martin ER; Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Hamilton-Nelson K; Department of Psychiatry, Washington University School of Medicine, St. Louis, MO, USA.
  • Shaw LM; Ronald M Loeb Center for Alzheimer's Disease, Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Trojanowski JQ; Neurogenomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.
  • Peskind ER; John T MacDonald Foundation Department of Human Genetics, University of Miami, Miami, FL, USA.
  • Cruchaga C; John P. Hussman Institute for Human Genomics, University of Miami School of Medicine, Miami, FL, USA.
  • Pericak-Vance MA; John P. Hussman Institute for Human Genomics, University of Miami School of Medicine, Miami, FL, USA.
  • Goate AM; Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Cox NJ; Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Haines JL; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA.
  • Zetterberg H; Department of Psychiatry, Washington University School of Medicine, St. Louis, MO, USA.
  • Blennow K; John P. Hussman Institute for Human Genomics, University of Miami School of Medicine, Miami, FL, USA.
  • Larson EB; Ronald M Loeb Center for Alzheimer's Disease, Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Johnson SC; Vanderbilt Genetics Institute, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Albert M; Department of Population and Quantitative Health Sciences, Institute for Computational Biology, Case Western Reserve University, Cleveland, OH, USA.
  • Bennett DA; Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal, Sweden.
  • Schneider JA; Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, UK.
  • Jefferson AL; UK Dementia Research Institute at UCL, London, UK.
  • Hohman TJ; Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, The Sahlgrenska Academy at University of Gothenburg, Mölndal, Sweden.
Brain ; 142(9): 2581-2589, 2019 09 01.
Article em En | MEDLINE | ID: mdl-31497858
Autopsy measures of Alzheimer's disease neuropathology have been leveraged as endophenotypes in previous genome-wide association studies (GWAS). However, despite evidence of sex differences in Alzheimer's disease risk, sex-stratified models have not been incorporated into previous GWAS analyses. We looked for sex-specific genetic associations with Alzheimer's disease endophenotypes from six brain bank data repositories. The pooled dataset included 2701 males and 3275 females, the majority of whom were diagnosed with Alzheimer's disease at autopsy (70%). Sex-stratified GWAS were performed within each dataset and then meta-analysed. Loci that reached genome-wide significance (P < 5 × 10-8) in stratified models were further assessed for sex interactions. Additional analyses were performed in independent datasets leveraging cognitive, neuroimaging and CSF endophenotypes, along with age-at-onset data. Outside of the APOE region, one locus on chromosome 7 (rs34331204) showed a sex-specific association with neurofibrillary tangles among males (P = 2.5 × 10-8) but not females (P = 0.85, sex-interaction P = 2.9 × 10-4). In follow-up analyses, rs34331204 was also associated with hippocampal volume, executive function, and age-at-onset only among males. These results implicate a novel locus that confers male-specific protection from tau pathology and highlight the value of assessing genetic associations in a sex-specific manner.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Caracteres Sexuais / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Estudo de Associação Genômica Ampla / Doença de Alzheimer Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Caracteres Sexuais / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Estudo de Associação Genômica Ampla / Doença de Alzheimer Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article