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Molecular psychiatry · 2023

Multi-ancestry meta-analysis and fine-mapping in Alzheimer's disease.

МетаанализСтатьяResearch Support, N.I.H., IntramuralПоддержка исследования: вне правительства СШАПоддержка NIH: внешняя программаНазвание и аннотация: Перевод в очереди
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Lake Julie, Warly Solsberg Caroline, Kim Jonggeol Jeffrey, Acosta-Uribe Juliana, Makarious Mary B, Li Zizheng, Levine Kristin, Heutink Peter, Alvarado Chelsea X, Vitale Dan, Kang Sarang, Gim Jungsoo, Lee Kun Ho, Pina-Escudero Stefanie D, Ferrucci Luigi, Singleton Andrew B, Blauwendraat Cornelis, Nalls Mike A, Yokoyama Jennifer S, Leonard Hampton L

Аннотация

Genome-wide association studies (GWAS) of Alzheimer's disease are predominantly carried out in European ancestry individuals despite the known variation in genetic architecture and disease prevalence across global populations. We leveraged published GWAS summary statistics from European, East Asian, and African American populations, and an additional GWAS from a Caribbean Hispanic population using previously reported genotype data to perform the largest multi-ancestry GWAS meta-analysis of Alzheimer's disease and related dementias to date. This method allowed us to identify two independent novel disease-associated loci on chromosome 3. We also leveraged diverse haplotype structures to fine-map nine loci with a posterior probability >0.8 and globally assessed the heterogeneity of known risk factors across populations. Additionally, we compared the generalizability of multi-ancestry- and single-ancestry-derived polygenic risk scores in a three-way admixed Colombian population. Our findings highlight the importance of multi-ancestry representation in uncovering and understanding putative factors that contribute to risk of Alzheimer's disease and related dementias.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты