Identification of Novel Genetic Loci Affecting Age at Onset of Parkinson's Disease: A Genome-wide Association Study

被引:1
作者
Hwang, Yun Su [1 ,2 ]
Jo, Sungyang [3 ]
Lee, Seung Hyun [4 ]
Park, Kye Won [5 ]
Shin, Eunsoon [6 ]
Park, Yoongi [6 ]
Seo, Yunji [6 ]
Kwon, Kyum-Yil [7 ]
Kim, Jae Seung [8 ]
Jeon, Sang Ryong [9 ]
Lee, Jae-Hong [3 ]
Chung, Sun Ju [3 ]
机构
[1] Jeonbuk Natl Univ, Med Sch & Hosp, Dept Neurol, Jeonju, South Korea
[2] Jeonbuk Natl Univ, Jeonbuk Natl Univ Hosp, Biomed Res Inst, Res Inst Clin Med, Jeonju, South Korea
[3] Univ Ulsan, Asan Med Ctr, Coll Med, Dept Neurol, 88 Olymp Ro 43 Gil, Seoul, South Korea
[4] Jeju Natl Univ, Jeju Natl Univ Hosp, Sch Med, Dept Neurol, Jeju, South Korea
[5] Univ Ulsan, Gangneung Asan Hosp, Coll Med, Dept Neurol, Kangnung, South Korea
[6] DNA Link, Seoul, South Korea
[7] Soonchunhyang Univ, Seoul Hosp, Dept Neurol, Seoul, South Korea
[8] Univ Ulsan, Asan Med Ctr, Coll Med, Dept Nucl Med, Seoul, South Korea
[9] Univ Ulsan, Asan Med Ctr, Coll Med, Dept Neurosurg, Seoul, South Korea
关键词
age at onset; genome-wide association study; Parkinson's disease; polygenic risk score; RISK-FACTORS; METAANALYSIS; EPIDEMIOLOGY; MODIFIER;
D O I
10.1002/mds.30047
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BackgroundThe age at onset (AAO) of Parkinson's disease (PD) varies widely among individuals and significantly influences disease progression and prognosis. However, few genome-wide association studies (GWASs) have investigated genetic variants determining AAO, particularly in East Asian populations. ObjectivesTo identify single-nucleotide polymorphisms (SNPs) affecting AAO of PD in Korean patients. MethodsWe conducted a GWAS on AAO of PD in 1048 Korean patients using sex-adjusted linear regression models. Additionally, we conducted downstream analyses of our primary GWAS results. Resultsrs2134545 demonstrated genome-wide significance (beta = -2.459; standard error [SE] = 0.851; P = 1.898 x 10-8) and is an intergenic SNP near the ALCAM gene associated with an average AAO reduction of 3.47 years. Additionally, rs4366309 (LYST; MIR1537) demonstrated suggestive significance (beta = 2.949; SE = 1.072; P = 8.68 x 10-8) and was associated with an average delay of 3.05 years. The polygenic risk score based on known PD risk loci also affected the AAO for European and Korean PD risk loci, respectively (beta = -0.149; P < 0.001 and beta = -0.096; P = 0.002). However, the proportion of variance was small (r2 = 0.022 and 0.009, respectively). ConclusionWe identified a novel SNP associated with the AAO of PD near the ALCAM gene, distinct from previously reported PD risk loci. These findings need further functional validation; however, they suggest unique genetic pathways influencing the AAO of PD and highlight the need for further research in diverse populations. (c) 2024 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
引用
收藏
页码:77 / 86
页数:10
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