Literature DB >> 31497858

Sex differences in the genetic predictors of Alzheimer's pathology.

Logan Dumitrescu1,2, Lisa L Barnes3, Madhav Thambisetty4, Gary Beecham5,6, Brian Kunkle6, William S Bush7, Katherine A Gifford1, Lori B Chibnik8,9, Shubhabrata Mukherjee10, Philip L De Jager11,12, Walter Kukull13, Paul K Crane10, Susan M Resnick4, C Dirk Keene14, Thomas J Montine15, Gerard D Schellenberg16, Yuetiva Deming17, Michael J Chao18, Matt Huentelman19, Eden R Martin5,6, Kara Hamilton-Nelson6, Leslie M Shaw16, John Q Trojanowski16, Elaine R Peskind20, Carlos Cruchaga17, Margaret A Pericak-Vance6, Alison M Goate18, Nancy J Cox2, Jonathan L Haines7, Henrik Zetterberg21,22,23,24, Kaj Blennow21,22, Eric B Larson10,25, Sterling C Johnson26, Marilyn Albert27, David A Bennett3, Julie A Schneider3, Angela L Jefferson1, Timothy J Hohman1,2.   

Abstract

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.
© The Author(s) (2019). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  Alzheimer’s disease; beta-amyloid; genome-wide association study; neuropathology; tau

Mesh:

Substances:

Year:  2019        PMID: 31497858      PMCID: PMC6736148          DOI: 10.1093/brain/awz206

Source DB:  PubMed          Journal:  Brain        ISSN: 0006-8950            Impact factor:   13.501


  30 in total

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