Key variants via the Alzheimer's Disease Sequencing Project whole genome sequence data.
Alzheimers Dement
; 20(5): 3290-3304, 2024 05.
Article
em En
| MEDLINE
| ID: mdl-38511601
ABSTRACT
INTRODUCTION:
Genome-wide association studies (GWAS) have identified loci associated with Alzheimer's disease (AD) but did not identify specific causal genes or variants within those loci. Analysis of whole genome sequence (WGS) data, which interrogates the entire genome and captures rare variations, may identify causal variants within GWAS loci.METHODS:
We performed single common variant association analysis and rare variant aggregate analyses in the pooled population (N cases = 2184, N controls = 2383) and targeted analyses in subpopulations using WGS data from the Alzheimer's Disease Sequencing Project (ADSP). The analyses were restricted to variants within 100 kb of 83 previously identified GWAS lead variants.RESULTS:
Seventeen variants were significantly associated with AD within five genomic regions implicating the genes OARD1/NFYA/TREML1, JAZF1, FERMT2, and SLC24A4. KAT8 was implicated by both single variant and rare variant aggregate analyses.DISCUSSION:
This study demonstrates the utility of leveraging WGS to gain insights into AD loci identified via GWAS.Palavras-chave
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Estudo de Associação Genômica Ampla
/
Doença de Alzheimer
/
Sequenciamento Completo do Genoma
Limite:
Aged
/
Female
/
Humans
/
Male
Idioma:
En
Ano de publicação:
2024
Tipo de documento:
Article