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帕金森病中基因多态性与抑郁的关联:一项病例对照研究。

Association between gene polymorphism and depression in Parkinson's disease: A case-control study.

作者信息

Zheng Jinhua, Yang Xinglong, Zhao Quanzhen, Tian Sijia, Huang Hongyan, Chen Yalan, Xu Yanming

机构信息

Department of Neurology, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, Sichuan Province 610041, PR China.

Department of Neurology, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, Sichuan Province 610041, PR China.

出版信息

J Neurol Sci. 2017 Apr 15;375:231-234. doi: 10.1016/j.jns.2017.02.001. Epub 2017 Feb 3.

DOI:10.1016/j.jns.2017.02.001
PMID:28320136
Abstract

OBJECTIVE

To investigate possible associations of Parkinson's disease (PD) with polymorphism in depression-related genes and in the alpha-synuclein (SNCA) gene.

METHODS

A consecutive series of patients with PD were divided into those with depression and those without it. Patients (330) were genotyped at four single-nucleotide polymorphisms (SNPs) in four genes previously associated with depression, as well as four SNPs in the PD-associated SNCA gene.

RESULTS

Of 330 patients, 125 (37.9%) had depression and 205 (62.1%) did not. Univariate analysis revealed significant differences between the two groups in minor allele frequency at the SNP rs1545843 in the SLC6A15 gene (p<0.05), as well as in frequencies of genotypes and minor alleles at rs78162420 in the TPH2 gene (all p<0.05). Logistic regression identified the following risk factors for depression among patients with PD: Hoehn and Yahr stage>2 (OR 1.759, 95%CI 1.035-2.989, p=0.037), AA genotype at rs1545843 (OR 1.866, 95%CI 1.017-3.426, p=0.044), and AC genotype at rs78162420 (OR 5.036, 95%CI 1.451-17.484, p=0.011).

CONCLUSIONS

Among patients with PD, depression is associated with polymorphism at rs78162420 and rs1545843, both previously linked with depression. Our results may help clarify the pathogenesis of depression in PD.

摘要

目的

研究帕金森病(PD)与抑郁相关基因及α-突触核蛋白(SNCA)基因多态性之间可能存在的关联。

方法

将连续纳入的PD患者分为伴抑郁组和不伴抑郁组。对330例患者进行了4个先前与抑郁相关基因的单核苷酸多态性(SNP)以及PD相关SNCA基因的4个SNP的基因分型。

结果

330例患者中,125例(37.9%)有抑郁,205例(62.1%)无抑郁。单因素分析显示,两组在溶质载体家族6成员15(SLC6A15)基因的SNP rs1545843的次要等位基因频率上存在显著差异(p<0.05),以及在色氨酸羟化酶2(TPH2)基因的rs78162420的基因型和次要等位基因频率上也存在显著差异(均p<0.05)。逻辑回归确定了PD患者抑郁的以下危险因素:Hoehn和Yahr分期>2(比值比[OR]1.759,95%置信区间[CI]1.035 - 2.989,p = 0.037)、rs1545843的AA基因型(OR 1.866,95%CI 1.017 - 3.426,p = 0.044)以及rs78162420的AC基因型(OR 5.036,95%CI 1.451 - 17.484,p = 0.011)。

结论

在PD患者中,抑郁与rs78162420和rs1545843的多态性相关,这两个位点先前均与抑郁有关。我们的结果可能有助于阐明PD中抑郁的发病机制。

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