Akgun Bilcag, Feliciano-Astacio Briseida E, Hamilton-Nelson Kara L, Scott Kyle, Rivero Joe, Adams Larry D, Sanchez Jose J, Valladares Glenies S, Tejada Sergio, Bussies Parker L, Silva-Vergara Concepcion, Rodriguez Vanessa C, Mena Pedro R, Celis Katrina, Whitehead Patrice G, Prough Michael, Kosanovic Christina, Van Booven Derek J, Schmidt Michael A, Acosta Heriberto, Griswold Anthony J, Dalgard Clifton L, McInerney Katalina F, Beecham Gary W, Cuccaro Michael L, Vance Jeffery M, Pericak-Vance Margaret A, Rajabli Farid
John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, United States.
Universidad Central del Caribe, Bayamón, PR, United States.
Front Aging Neurosci. 2024 Sep 4;16:1459796. doi: 10.3389/fnagi.2024.1459796. eCollection 2024.
Hispanic/Latino populations are underrepresented in Alzheimer Disease (AD) genetic studies. Puerto Ricans (PR), a three-way admixed (European, African, and Amerindian) population is the second-largest Hispanic group in the continental US. We aimed to conduct a genome-wide association study (GWAS) and comprehensive analyses to identify novel AD susceptibility loci and characterize known AD genetic risk loci in the PR population.
Our study included Whole Genome Sequencing (WGS) and phenotype data from 648 PR individuals (345 AD, 303 cognitively unimpaired). We used a generalized linear-mixed model adjusting for sex, age, population substructure, and genetic relationship matrix. To infer local ancestry, we merged the dataset with the HGDP/1000G reference panel. Subsequently, we conducted univariate admixture mapping (AM) analysis.
We identified suggestive signals within the and genes on chromosome 12q13. This region overlaps with an area of linkage of AD in previous studies (12q13) in independent data sets further supporting. Univariate African AM analysis identified one suggestive ancestral block ( = 7.2×10) located in the same region. The ancestry-aware approach showed that this region has both European and African ancestral backgrounds and both contributing to the risk in this region. We also replicated 11 different known AD loci -including - identified in mostly European studies, which is likely due to the high European background of the PR population.
PR GWAS and AM analysis identified a suggestive AD risk locus on chromosome 12, which includes the and genes. Our findings demonstrate the importance of designing GWAS and ancestry-aware approaches and including underrepresented populations in genetic studies of AD.
西班牙裔/拉丁裔人群在阿尔茨海默病(AD)基因研究中的代表性不足。波多黎各人(PR)是一个具有欧洲、非洲和美洲印第安人三方混合血统的群体,是美国大陆第二大西班牙裔群体。我们旨在进行全基因组关联研究(GWAS)和综合分析,以识别新的AD易感基因座,并对PR人群中已知的AD遗传风险基因座进行特征描述。
我们的研究包括来自648名PR个体(345名AD患者,303名认知未受损者)的全基因组测序(WGS)和表型数据。我们使用了一个广义线性混合模型,对性别、年龄、人群亚结构和遗传关系矩阵进行了调整。为了推断本地祖先,我们将数据集与HGDP/1000G参考面板合并。随后,我们进行了单变量混合映射(AM)分析。
我们在12号染色体q13区域的 和 基因内发现了提示性信号。该区域与先前独立数据集中AD的一个连锁区域(12q13)重叠,进一步支持了这一发现。单变量非洲AM分析在同一区域确定了一个提示性祖先块( = 7.2×10)。祖先意识方法表明,该区域具有欧洲和非洲祖先背景,两者都对该区域的风险有贡献。我们还复制了11个不同的已知AD基因座,包括在大多数欧洲研究中确定的基因座,这可能是由于PR人群中欧洲背景较高。
PR GWAS和AM分析在12号染色体上确定了一个提示性AD风险基因座,其中包括 和 基因。我们的研究结果证明了设计GWAS和祖先意识方法以及将代表性不足的人群纳入AD基因研究的重要性。