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GWAS Study

Genome-wide association study of language performance in Alzheimer's disease.

Deters KD, Nho K, Risacher SL et al.

28577822 PubMed ID
GWAS Study Type
1560 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

DK
Deters KD
NK
Nho K
RS
Risacher SL
KS
Kim S
RV
Ramanan VK
CP
Crane PK
AL
Apostolova LG
SA
Saykin AJ
Chapter II

Abstract

Summary of the research findings

Language impairment is common in prodromal stages of Alzheimer's disease (AD) and progresses over time. However, the genetic architecture underlying language performance is poorly understood. To identify novel genetic variants associated with language performance, we analyzed brain MRI and performed a genome-wide association study (GWAS) using a composite measure of language performance from the Alzheimer's Disease Neuroimaging Initiative (ADNI; n=1560). The language composite score was associated with brain atrophy on MRI in language and semantic areas. GWAS identified GLI3 (GLI family zinc finger 3) as significantly associated with language performance (p<5×10-8). Enrichment of GWAS association was identified in pathways related to nervous system development and glutamate receptor function and trafficking. Our results, which warrant further investigation in independent and larger cohorts, implicate GLI3, a developmental transcription factor involved in patterning brain structures, as a putative gene associated with language dysfunction in AD.

310 European ancestry Alzheimer's disease individuals, 511 European ancestry individuals with late mild cognitive impairment, 280 European ancestry individuals with early mild cognitive impairment, 94 European ancestry individuals with significant memory concern, 365 European ancestry individuals with normal cognition

Chapter III

Study Statistics

Key metrics and study information

1560
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Canada, U.S.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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