期刊文献+

新疆地区帕金森病遗传易感性与COMT和CYP1A1基因多态性相互关系的研究 被引量:7

The correlation research among the polymorphisms of COMT gene,CYP 1A1 gene and Parkinson disease in Xinjiang
暂未订购
导出
摘要 目的探讨儿茶酚胺氧位甲基转移酶(catechol-O-methyltransferase,COMT)基因G1947A多态性和细胞色素P450 1A1(cytochrome P4501A1,CYP 1A1)基因Msp I多态的独立及其协同作用与新疆地区帕金森病(Parkinson’s disease,PD)遗传易感性的关系。方法应用聚合酶链反应-限制性片段长度多态性分析法(PCRRFLP)分析新疆地区237例散发性PD患者和247例健康对照者的COMT基因G1947A多态性、CYP 1A1基因Msp I多态性。结果 (1)COMT基因G1947A多态性、CYP 1A1基因Msp I多态性分布在PD组与对照组间无统计学差异(均P>0.05)。均按民族、性别、年龄分层后,两种基因的多态性分布在各亚组PD组和对照组间无统计学差异(均P>0.05)。(2)COMT G/G基因型和CYP 1A1 T/T基因型间的协同作用可使新疆维吾尔族人群中PD的发生风险增加3.288倍(OR=3.288)。(3)COMT G/G基因型与CYP 1A1 T/C基因型间的协同作用可分别使新疆维吾尔族人群中、年龄≥60岁人群中PD的发生风险下降0.245倍、0.451倍(维吾尔族人群:OR=0.245、年龄≥60岁人群:OR=0.451)。结论 COMT基因、CYP 1A1基因不同基因型间的协同作用可增加或减少新疆地区部分人群PD的发生风险。 Objective To explore the independent and synergic role between the polymorphisms of catechol-o-meth- yltransferase (COMT) gene G1947A and cytochrome P4501A1 (CYP1A1) gene Msp I in genetic susceptibility to Parkinson disease (PD) in Xinjiang region. Methods The polymorphisms of COMT gene and CYP1 A1 gene was determined by pol- ymerase chain-reaction restriction fragment length polymorphism (PCR-RFLP) in 237 idiopathic PD patients and 247 health controls in Xinjiang region. Results ( 1 ) There is no statistical difference in the distribution of the polymorphism of COMT gene and CYP1 A1 gene between PD group and control group ( all P 〉 0.05 ). stratified by nationality, gender and age, there is no statistical difference with the distribution of the polymorphism of both gene between each subgroup of PD group and control group ( all P 〉 0.05 ). (2) Synergistic effect of G/G genotype of COMT gene and T/T genotype of CYP1 A1 gene was associated with a 3. 288-fold increased relative risk of PD of Uygurs in Xinjiang ( OR = 3. 288 ). ( 3 ) Synergistic effect of G/ G genotype of COMT gene and T/C genotype of CYP1A1 gene was separately associated with a 0. 245-fold and 0.451-fold decreased relative risk of PD of Uygurs and age ≥60 years old people in Xinjiang( Uygurs: OR = 0. 245 .age 〉/60 years old:OR = 0.451 ). Conclusion The synergistic function of the polymorphism of COMT gene and CYP1 A1 gene might be increase or decrease the risk of PD of some population in Xinjiang region.
出处 《中风与神经疾病杂志》 CAS CSCD 北大核心 2014年第2期153-157,共5页 Journal of Apoplexy and Nervous Diseases
基金 兵团科技计划资助项目(No.2011BA047)
关键词 帕金森病 COMT基因 CYP 1A1基因 多态性 Parkinson' s disease COMT gene CYP1 A1 gene Polymorphism
  • 相关文献

参考文献8

二级参考文献34

  • 1Chan P,J Neurochem,1991年,57卷,348页
  • 2陈彪,遗传与疾病,1989年,6卷,87页
  • 3王建,中华医学遗传学杂志,1999年,16卷,406页
  • 4Leighton P W,Neurology,1997年,49卷,1577页
  • 5Li T,Psychol Res,1994年,52卷,17页
  • 6Kang A M,BioPsychiatry,1999年,46卷,151页
  • 7Hernan MA,Checkoway H,O' Brien R,et al. MAOB intron 13 and COMT codon158 polymorphisms,cigarette smoking,and the risk of PD. Neurology 2002; 58(9): 1381 -7.
  • 8Healy DG,Abou-Sleiman PM,Ozawa T,et al. A functional polymorphism regulating dopamine beta-hydroxylase influences against Parkinson's disease. Ann Neurol 2004; 55(3): 443 -6.
  • 9O' Connor DT,Cervenka JH,Stone RA,et al. Dopamine beta-hydroxylase immunoreactivity in human cerebrospinal fluid: properties,relationship to central noradrenergic neuronal activity and variation in Parkinson' s disease and congenital dopamine beta-hydroxylase deficiency. Clin Sci (Lond) 1994; 86(2): 149 -58.
  • 10Kunugi H,Nanko S,Ueki A,et al. High and low activity alleles of catechol-O-methyltransferase gene: ethnic difference and possible association with Parkinson' s disease. Neurosci Lett 1997; 221 (2 - 3 ): 202 - 4.

共引文献52

同被引文献72

  • 1卢芳,周世慧,刘树民.帕金森病致病基因的研究进展[J].中国老年学杂志,2014,34(5):1411-1413. 被引量:4
  • 2江小华,徐群渊,杨慧,陈彪.中国人群单胺氧化酶-B基因多态性与帕金森病相关性研究[J].中华神经科杂志,2004,37(3):239-242. 被引量:5
  • 3Klebe S, GolmardJL, Nalls MA, et al. The Vall58Met COMT polymorphism is a modifier of the age at onset in Parkinson' s disease with a sexual dimorphism[J].J Neurol Neurosurg Psychiatry, 2013, 84 (6) : 666-673.
  • 4Kunugi H, Nanko S, Veki A, et al. High and low activity alleles of catechol O-methyltransferase gene: ethnic difference and possible association with Parkinson's disease[J]. Neurosci Lett, 1997, 221 (2-3): 202-204.
  • 5MassanoJ, Bhatia KP. Clinical approach to Parkinson's disease: features, diagnosis, and principles of management[J]. Cold Spring Harb Perspect Med, 2012, 2 (6) : a008870.
  • 6Rundell MS, Pingle M, Das S, et al. A multiplex PCR/LDR assay for simultaneous detection and identification of the NIAID category B bacterial food and water-borne pathogens[J]. Diagn Microbiol Infect Dis, 2014, 79 (2) : l35-140.
  • 7de Lau LM, Breteler MM. Epidemiology of Parkinson's disease[J]. Lancet Neurol, 2006, 5 (6) : 525 -535.
  • 8Torkaman-Boutorabi A, Ali Shahidi G, Choopani S, et al. Association of monoamine oxidase Band catechol-Omethyltransferase polymorphisms with sporadic Parkinson' s disease in an Iranian population[J]. Folia Neuropathol, 2012, 50 (4) : 382-389.
  • 9Wang Y, Yang X. Association of catechol-O-methyltranferase polymorphism (Vall 08/158 Met) with Parkinson' s disease: a meta-analysisJ J].J Mot Behav, 2012, 44 (5): 365-372.
  • 10Jimenez-Jimenez FJ, Alonso-Navarro H, Carota-Martfn E, et al. COMT gene and risk for Parkinson's disease: a systematic review and meta-analysis[J], Pharmacogenet Genomics, 2014, 24 (7) : 331-339.

引证文献7

二级引证文献11

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部