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GWAS Study

Genome-wide interaction study of brain beta-amyloid burden and cognitive impairment in Alzheimer's disease.

Roostaei T, Nazeri A, Felsky D et al.

27021820 PubMed ID
GWAS Study Type
1627 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

RT
Roostaei T
NA
Nazeri A
FD
Felsky D
DJ
De Jager PL
SJ
Schneider JA
PB
Pollock BG
BD
Bennett DA
VA
Voineskos AN
Chapter II

Abstract

Summary of the research findings

The lack of strong association between brain beta-amyloid deposition and cognitive impairment has been a challenge for the Alzheimer's disease (AD) field. Although beta-amyloid is necessary for the pathologic diagnosis of AD, it is not sufficient to make the pathologic diagnosis or cause dementia. We sought to identify the genetic modifiers of the relation between cortical beta-amyloid burden (measured using [18F]Florbetapir-PET) and cognitive dysfunction (measured using ADAS-cog) by conducting a genome-wide interaction study on baseline data from participants in the Alzheimer's Disease Neuroimaging Initiative (ADNI) phases GO/2 (n=678). Near genome-wide significant interaction effect was observed for rs73069071 within the IAPP (amylin) and SLCO1A2 genes (P=6.2 × 10-8). Congruent results were found using data from participants followed up from ADNI-1 (Pone-tailed=0.028, n=165). Meta-analysis across ADNI-GO/2 and ADNI-1 revealed a genome-wide significant interaction effect (P=1.1 × 10-8). Our results were further supported by similar interaction effects on temporal lobe cortical thickness (whole-brain voxelwise analysis: familywise error corrected P=0.013) and longitudinal changes in ADAS-cog score and left middle temporal thickness and amygdalar volume (Pone-tailed=0.026, 0.019 and 0.003, respectively). Using postmortem beta-amyloid immunohistochemistry data from 243 AD participants in the Religious Orders Study and Memory and Aging Project, we also observed similar rs73069071-by-beta-amyloid deposition interaction effect on global cognitive function (Pone-tailed=0.005). Our findings provide insight into the complexity of the relationship between beta-amyloid burden and AD-related cognitive impairment. Although functional studies are required to elucidate the role of rs73069071 in AD pathophysiology, our results support the recently growing evidence on the role of amylin in AD.

251 European ancestry early mild cases, 122 European ancestry late mild cases, 108 European ancestry Alzheimer's disease cases, 197 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

1627
Total Participants
GWAS
Study Type
Yes
Replicated
280 European ancestry mild cases, 287 European ancestry Alzheimer's disease cases, 382 European ancestry controls
Replication Participants
European
Ancestry
U.S.
Recruitment Country
Chapter IV

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