Leal Thiago P, French-Kwawu Jennifer N, Gouveia Mateus H, Borda Victor, Inca-Martinez Miguel, Mason Emily A, Horimoto Andrea Rvr, Loesch Douglas P, Sarihan Elif I, Cornejo-Olivas Mario R, Torres Luis E, Mazzetti-Soler Pilar E, Cosentino Carlos, Sarapura-Castro Elison H, Rivera-Valdivia Andrea, Medina Angel C, Dieguez Elena M, Raggio Víctor E, Lescano Andrés, Tumas Vitor, Borges Vanderci, Ferraz Henrique B, Rieder Carlos R, Schumacher-Schuh Artur, Santos-Lobato Bruno L, Velez-Pardo Carlos, Jimenez-Del-Rio Marlene, Lopera Francisco, Moreno Sonia, Chana-Cuevas Pedro, Fernandez William, Arboleda Gonzalo, Arboleda Humberto, Arboleda Bustos Carlos E, Yearout Dora, Lima-Costa Maria F, Tarazona Eduardo, Zabetian Cyrus, Thornton Timothy A, O'Connor Timothy D, Mata Ignacio F
medRxiv. 2023 Feb 2:2023.01.31.23285199. doi: 10.1101/2023.01.31.23285199.
Sex differences in Parkinson Disease (PD) risk are well-known. However, it is still unclear the role of sex chromosomes in the development and progression of PD. We performed the first X-chromosome Wide Association Study (XWAS) for PD risk in Latin American individuals. We used data from three admixed cohorts: (i) Latin American Research consortium on the GEnetics of Parkinson's Disease (n=1,504) as discover cohort and (ii) Latino cohort from International Parkinson Disease Genomics Consortium (n = 155) and (iii) Bambui Aging cohort (n= 1,442) as replication cohorts. After developing a X-chromosome framework specifically designed for admixed populations, we identified eight linkage disequilibrium regions associated with PD. We fully replicated one of these regions (top variant rs525496; discovery OR [95%CI]: 0.60 [0.478 - 0.77], p = 3.13 × ; replication OR: 0.60 [0.37-0.98], p = 0.04). rs525496 is an expression quantitative trait loci for several genes expressed in brain tissues, including and . We also replicated a previous XWAS finding (rs28602900), showing that this variant is associated with PD in non-European populations. Our results reinforce the importance of including X-chromosome and diverse populations in genetic studies.
帕金森病(PD)风险中的性别差异是众所周知的。然而,性染色体在PD发生和发展中的作用仍不清楚。我们针对拉丁美洲人群的PD风险进行了首次全X染色体关联研究(XWAS)。我们使用了来自三个混合队列的数据:(i)拉丁美洲帕金森病遗传学研究联盟(n = 1,504)作为发现队列,以及(ii)国际帕金森病基因组学联盟的拉丁裔队列(n = 155)和(iii)班布伊老龄化队列(n = 1,442)作为重复队列。在开发了专门为混合人群设计的X染色体框架后,我们确定了八个与PD相关的连锁不平衡区域。我们完全重复了其中一个区域(顶级变异rs525496;发现期优势比[95%置信区间]:0.60[0.478 - 0.77],p = 3.13×;重复期优势比:0.60[0.37 - 0.98],p = 0.04)。rs525496是几个在脑组织中表达的基因的表达数量性状位点,包括 和 。我们还重复了之前的一项XWAS研究结果(rs28602900),表明该变异在非欧洲人群中与PD相关。我们的结果强化了在基因研究中纳入X染色体和不同人群的重要性。