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囊泡单胺转运蛋白2基因多态性与帕金森病患者抑郁状态相关性的研究
引用本文:王芳,刘彬,邢冬梅,杨兴隆,李柯麓,吴崇明,保健见,任惠,徐忠.囊泡单胺转运蛋白2基因多态性与帕金森病患者抑郁状态相关性的研究[J].国际神经病学神经外科学杂志,2018,45(4):331-335.
作者姓名:王芳  刘彬  邢冬梅  杨兴隆  李柯麓  吴崇明  保健见  任惠  徐忠
作者单位:1. 昆明医科大学第一附属医院老年神经内科, 云南省昆明市 650032;2. 云南省第三人民医院神经内科, 云南省昆明市 650032
基金项目:四川科技厅应用基础研究项目(2014JY0247);昆明医科大学第一附属医院博士科研基金项目(2017BS005)
摘    要:目的 研究囊泡单胺转运蛋白2(VMAT2)的rs363371和rs363324基因多态性与汉族人群中PD患者合并抑郁状态的相关性。方法 收集102例汉族帕金森病(PD)患者,通过采用17项汉密尔顿抑郁量表(HAMD-17)将患者分为PD合并抑郁组和PD未合并抑郁组,用连接酶法对VMAT2的rs363371和rs363324进行了基因型分型,运用二元Logistic回归检验分析PD患者合并抑郁的危险因素。结果 rs363371的AA基因型降低了PD患者合并抑郁的风险(OR=0.22,59%CI 0.07-0.75,P=0.015)。UP3的高分值增加了PD患者合并抑郁的风险(OR=1.08,59%CI 1.02-1.15,P=0.009)。较长的病程增加了PD患者合并抑郁的风险(OR=1.15,59%CI 1.01-1.31,P=0.038)。rs363324的基因多态性并未增加PD合并抑郁的风险。结论 VMAT2的rs363371的AA基因型降低了汉族人群PD患者合并抑郁的风险。

关 键 词:帕金森病  VMAT2基因  抑郁  基因多态性  
收稿时间:2018-03-09
修稿时间:2018/7/18 0:00:00

Association between vesicular monoamine transporter 2 polymorphisms and depression in Parkinson's disease
WANG Fang,LIU Bin,XING Dong-Mei,YANG Xing-Long,LI Ke-Lu,WU Chong-Ming,BAO Jian-Jian,REN Hui,XU Zhong.Association between vesicular monoamine transporter 2 polymorphisms and depression in Parkinson's disease[J].Journal of International Neurology and Neurosurgery,2018,45(4):331-335.
Authors:WANG Fang  LIU Bin  XING Dong-Mei  YANG Xing-Long  LI Ke-Lu  WU Chong-Ming  BAO Jian-Jian  REN Hui  XU Zhong
Affiliation:Department of Geriatric Neurology, The First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan 650032, China
Abstract:Objective To investigate the association between vesicular monoamine transporter 2 (VMAT2) polymorphisms, rs363371 and rs363324, and depression in the Han Chinese population with Parkinson's disease (PD).Methods A total of 102 Han Chinese patients with PD were enrolled and divided into PD with depression group and PD without depression group according to the 17-item Hamilton Depression Rating Scale. The two single nucleotide polymorphisms (SNPs) of VMAT2, rs363371 and rs363324, were genotyped using ligase detection reaction. Binary logistic regression was used to analyze the risk factors for depression in PD.Results The AA genotype at rs363371 reduced the risk of depression in PDodds ratio (OR)=0.22, 95% confidence interval (CI):0.07-0.75, P=0.015]. The high score for UP3 increased the risk of depression in PD (OR=1.08, 95%CI:1.02-1.15, P=0.009). Long duration of PD increased the risk of depression in PD (OR=1.15, 95%CI:1.01-1.31, P=0.038). The VMAT2 SNP rs363324 did not increase the risk of depression in PD.Conclusions The AA genotype at rs363371 reduces the risk of depression in the Han Chinese population with PD.
Keywords:Parkinson's disease  vesicular monoamine transporter 2  depression  polymorphism  
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