TY - JOUR
T1 - Sex differences in the genetic predictors of Alzheimer’s pathology
AU - Alzheimer’s Disease Genetics Consortium
AU - Alzheimer’s Disease Neuroimaging Initiative
AU - Dumitrescu, Logan
AU - Barnes, Lisa L.
AU - Thambisetty, Madhav
AU - Beecham, Gary
AU - Kunkle, Brian
AU - Bush, William S.
AU - Gifford, Katherine A.
AU - Chibnik, Lori B.
AU - Mukherjee, Shubhabrata
AU - de Jager, Philip L.
AU - Kukull, Walter
AU - Crane, Paul K.
AU - Resnick, Susan M.
AU - Dirk Keene, C.
AU - Montine, Thomas J.
AU - Schellenberg, Gerard D.
AU - Deming, Yuetiva
AU - Chao, Michael J.
AU - Huentelman, Matt
AU - Martin, Eden R.
AU - Hamilton-Nelson, Kara
AU - Shaw, Leslie M.
AU - Trojanowski, John Q.
AU - Peskind, Elaine R.
AU - Cruchaga, Carlos
AU - Pericak-Vance, Margaret A.
AU - Goate, Alison M.
AU - Cox, Nancy J.
AU - Haines, Jonathan L.
AU - Zetterberg, Henrik
AU - Blennow, Kaj
AU - Larson, Eric B.
AU - Johnson, Sterling C.
AU - Albert, Marilyn
AU - Bennett, David A.
AU - Schneider, Julie A.
AU - Jefferson, Angela L.
AU - Hohman, Timothy J.
N1 - Publisher Copyright:
© The Author(s) (2019). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved.
PY - 2019/9/1
Y1 - 2019/9/1
N2 - 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.
AB - 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.
KW - Alzheimer’s disease
KW - Beta-amyloid
KW - Genome-wide association study
KW - Neuropathology
KW - Tau
UR - http://www.scopus.com/inward/record.url?scp=85071989648&partnerID=8YFLogxK
U2 - 10.1093/brain/awz206
DO - 10.1093/brain/awz206
M3 - Article
C2 - 31497858
AN - SCOPUS:85071989648
SN - 0006-8950
VL - 142
SP - 2581
EP - 2589
JO - Brain
JF - Brain
IS - 9
ER -