Exploring the Genetic Architecture of Parkinson's Disease in a SouthernSpanish Population

B. Sara, rés Ciga, C. Ruz, F. Barrero, F. Sevilla, Javier Pelegrina, M. Ramı́rez, F. Vives, R. Durán
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Abstract

In the recent years, the emergence of new technologies has revolutionized our concepts to identify genetic mechanisms implicated in Parkinson's disease (PD). Genome-wide association studies (GWAS) have been key in such enormous advance. To the best of our knowledge we have conducted the first GWAS of PD in a Spanish population. We replicated the association of 5 reported PD-related loci at nominal p-value, and our cumulative risk score was consistent with studies performed in other European populations. We did not manage to identify any novel rare variant through single variant and gene-based tests and we assume that there may be structural genomic variation conferring risk for PD poorly covered or undetectable by the array. We conclude that in complex genetic disorders such as PD, collaboration drives progress and real advances can only be made by large consortiums cooperating with collaborative spirit. In the years to come, interpretation of the risk in the context of disease pathogenesis will be the main goal to reach.
在西班牙南部人群中探索帕金森病的遗传结构
近年来,新技术的出现彻底改变了我们识别与帕金森病(PD)有关的遗传机制的概念。全基因组关联研究(GWAS)是取得如此巨大进步的关键。据我们所知,我们已经在西班牙人群中进行了第一次PD GWAS。我们以名义p值重复了5个报告的pd相关基因座的关联,我们的累积风险评分与在其他欧洲人群中进行的研究一致。我们没有通过单变异和基于基因的测试发现任何新的罕见变异,我们假设可能存在结构基因组变异,导致PD的风险被阵列覆盖不足或无法检测到。我们的结论是,在PD等复杂的遗传疾病中,合作推动进步,真正的进步只能通过具有协作精神的大型财团合作来实现。在未来几年,在疾病发病机制的背景下解释风险将是要达到的主要目标。
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