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rs1375206 多态性与血浆 ATG7 水平升高与中国南方汉族散发性晚发性帕金森病的关联。

Associations of rs1375206 polymorphism and elevated plasma ATG7 levels with late-onset sporadic Parkinson's disease in a cohort of Han Chinese from southern China.

机构信息

Department of Neurology, The Second Affiliated Hospital (Jiande Branch), School of Medicine, Zhejiang University, Hangzhou, Zhejiang Province, China.

Department of Neurology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong Province, China.

出版信息

Int J Neurosci. 2020 Dec;130(12):1206-1214. doi: 10.1080/00207454.2020.1731507. Epub 2020 Feb 24.

DOI:10.1080/00207454.2020.1731507
PMID:32065549
Abstract

Autophagy-related gene 7 (ATG7) plays a key role in autophagy and is strongly implicated in Parkinson's disease (PD). This study investigated the associations of rs1375206 polymorphism in gene promoter and plasma ATG7 levels with late-onset sporadic PD in a cohort of Han Chinese from southern China. Variant genotypes were identified using polymerase chain reaction-restriction fragment length polymorphism and gene sequencing in 124 patients with late-onset sporadic PD, as well as in 105 age- and sex-matched healthy controls. Plasma ATG7 levels were determined using an enzyme-linked immunosorbent assay. No significant differences in genotype distributions were found between the two groups. Stratification analyses by sex and clinical motor subtypes revealed that the differences remained non-significant in each subgroup (all  > 0.05). Plasma ATG7 protein levels were significantly higher in the PD group than in the control group ( = 0.000). Haplotype analysis demonstrated that the A-T haplotype was significantly associated with late-onset sporadic PD ( = 0.045). Our study suggests that the rs1375206 polymorphism in may not be associated with late-onset sporadic PD; however, high plasma ATG7 levels and the A-T haplotype may be associated with susceptibility to late-onset sporadic PD in the Han population from Zhejiang and Guangdong provinces.

摘要

自噬相关基因 7(ATG7)在自噬中发挥关键作用,并且强烈提示其与帕金森病(PD)有关。本研究在中国南方汉族人群中,研究了基因启动子中 rs1375206 多态性与血浆 ATG7 水平与迟发性散发性 PD 之间的关联。通过聚合酶链反应-限制性片段长度多态性和基因测序,在 124 例迟发性散发性 PD 患者和 105 例年龄和性别匹配的健康对照者中确定了变异基因型。使用酶联免疫吸附测定法测定血浆 ATG7 水平。两组之间的基因型分布无显着差异。按性别和临床运动亚型分层分析显示,每个亚组的差异均无统计学意义(均>0.05)。PD 组的血浆 ATG7 蛋白水平明显高于对照组(=0.000)。单体型分析表明,A-T 单体型与迟发性散发性 PD 显着相关(=0.045)。我们的研究表明,基因中的 rs1375206 多态性可能与迟发性散发性 PD 无关;然而,高血浆 ATG7 水平和 A-T 单体型可能与浙粤汉族人群中迟发性散发性 PD 的易感性有关。

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