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GWAS Study

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

Dumitrescu L, Barnes LL, Thambisetty M et al.

31497858 PubMed ID
GWAS Study Type
5976 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

DL
Dumitrescu L
BL
Barnes LL
TM
Thambisetty M
BG
Beecham G
KB
Kunkle B
BW
Bush WS
GK
Gifford KA
CL
Chibnik LB
MS
Mukherjee S
DJ
De Jager PL
KW
Kukull W
CP
Crane PK
RS
Resnick SM
KC
Keene CD
MT
Montine TJ
SG
Schellenberg GD
DY
Deming Y
CM
Chao MJ
HM
Huentelman M
ME
Martin ER
HK
Hamilton-Nelson K
SL
Shaw LM
TJ
Trojanowski JQ
PE
Peskind ER
CC
Cruchaga C
PM
Pericak-Vance MA
GA
Goate AM
CN
Cox NJ
HJ
Haines JL
ZH
Zetterberg H
BK
Blennow K
LE
Larson EB
JS
Johnson SC
AM
Albert M
BD
Bennett DA
SJ
Schneider JA
JA
Jefferson AL
HT
Hohman TJ
Chapter II

Abstract

Summary of the research findings

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.

2,701 European ancestry men, 3,275 European ancestry women

Chapter III

Study Statistics

Key metrics and study information

5976
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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