Whole‐genome sequencing study in Koreans identifies novel loci for Alzheimer's disease

INTRODUCTION The genetic basis of Alzheimer's disease (AD) in Koreans is poorly understood. METHODS We performed an AD genome‐wide association study using whole‐genome sequence data from 3540 Koreans (1583 AD cases, 1957 controls) and single‐nucleotide polymorphism array data from 2978 Japanese...

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Veröffentlicht in:Alzheimer's & dementia 2024-12, Vol.20 (12), p.8246-8262
Hauptverfasser: Kang, Moonil, Farrell, John J., Zhu, Congcong, Park, Hyeonseul, Kang, Sarang, Seo, Eun Hyun, Choi, Kyu Yeong, Jun, Gyungah R., Won, Sungho, Gim, Jungsoo, Lee, Kun Ho, Farrer, Lindsay A.
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Sprache:eng
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Zusammenfassung:INTRODUCTION The genetic basis of Alzheimer's disease (AD) in Koreans is poorly understood. METHODS We performed an AD genome‐wide association study using whole‐genome sequence data from 3540 Koreans (1583 AD cases, 1957 controls) and single‐nucleotide polymorphism array data from 2978 Japanese (1336 AD cases, 1642 controls). Significant findings were evaluated by pathway enrichment and differential gene expression analysis in brain tissue from controls and AD cases with and without dementia prior to death. RESULTS We identified genome‐wide significant associations with APOE in the total sample and ROCK2 (rs76484417, p = 2.71×10−8) among APOE ε4 non‐carriers. A study‐wide significant association was found with aggregated rare variants in MICALL1 (MICAL like 1) (p = 9.04×10−7). Several novel AD‐associated genes, including ROCK2 and MICALL1, were differentially expressed in AD cases compared to controls (p 
ISSN:1552-5260
1552-5279
1552-5279
DOI:10.1002/alz.14128