Zhu Wenqing, Luo Xiaoguang, Adnan Atif, Yu Peifu, Zhang Siyi, Huo Zhixin, Xu Qin, Pang Hao
School of Forensic Medicine, China Medical University.
Department of Neurology, First Affiliated Hospital of China Medical University.
Genes Genet Syst. 2018 Sep 15;93(2):59-64. doi: 10.1266/ggs.17-00038. Epub 2018 Mar 30.
Genome-wide association studies have reported numerous candidate loci associated with Parkinson's disease (PD). NUCKS1 and INPP5K are two such candidate loci, although they have rarely been reported in Asian populations. To explore these potential genes for PD susceptibility, we investigated the association between PD and two SNPs, rs823114 and rs1109303, located on the NUCKS1 and INPP5K genes, respectively, in the Han population of northern China. We genotyped the two SNPs using the multiplex PCR-RFLP (polymerase chain reaction-restriction fragment length polymorphism) technique. A total of 685 subjects including 322 sporadic PD patients and 363 healthy controls were recruited from the population. After Bonferroni correction, our results suggested that there was a significant association of a minor allele (G) in rs823114 with reduced risk of PD development (P = 0.017, OR = 0.768, 95%CI = 0.618 - 0.955), and the difference in genotypes between the PD patients and healthy controls was significant under the dominant model (GA + GG vs. AA). After stratification by gender, males had a lower risk than females (P = 0.008, OR = 0.666, 95%CI = 0.495 - 0.898). However, the distribution of genotype frequency exhibited no significant differences between the PD and control groups (P > 0.025) in INPP5K rs1109303 (P = 0.048, OR = 0.806, 95%CI = 0.650 - 0.998). We conclude that NUCKS1 rs823114 indicates a decreased risk of susceptibility to PD and shows a male genetic distribution bias in the Han Chinese population.
全基因组关联研究已经报道了许多与帕金森病(PD)相关的候选基因座。NUCKS1和INPP5K就是这样两个候选基因座,尽管它们在亚洲人群中鲜有报道。为了探究这些与PD易感性相关的潜在基因,我们在中国北方汉族人群中研究了PD与分别位于NUCKS1和INPP5K基因上的两个单核苷酸多态性(SNP),即rs823114和rs1109303之间的关联。我们使用多重聚合酶链反应-限制性片段长度多态性(PCR-RFLP)技术对这两个SNP进行基因分型。共从该人群中招募了685名受试者,包括322例散发性PD患者和363名健康对照。经过Bonferroni校正后,我们的结果表明,rs823114中的一个次要等位基因(G)与PD发病风险降低显著相关(P = 0.017,OR = 0.768,95%CI = 0.618 - 0.955),并且在显性模型(GA + GG与AA)下,PD患者和健康对照之间的基因型差异显著。按性别分层后,男性的风险低于女性(P = 0.008,OR = 0.666,95%CI = 0.495 - 0.898)。然而,在INPP5K rs1109303中,PD组和对照组之间的基因型频率分布没有显著差异(P > 0.025)(P = 0.048,OR = 0.806,95%CI = 0.650 - 0.998)。我们得出结论,NUCKS1 rs823114表明汉族人群中PD易感性风险降低,并显示出男性遗传分布偏向。