首都医科大学学报 ›› 2008, Vol. 29 ›› Issue (3): 278-282.

• 专题报道 • 上一篇    下一篇

尿激酶型纤溶酶原激活因子基因P141L多态性与迟发性阿尔茨海默病的关系

向绍通1, 徐书雯1, 李东风2   

  1. 1. 广东省人民医院老年医学研究所神经内科;2. 广东省人民医院医学研究中心
  • 收稿日期:2008-04-16 修回日期:1900-01-01 出版日期:2008-06-24 发布日期:2008-06-24
  • 通讯作者: 徐书雯

Relation between the P141L Polymorphism of Urokinase Plasminogen Activator Gene and Late-onset Alzheimer's Disease

Xiang Shaotong1, Xu Shuwen1, Li Dongfeng2   

  1. 1. Department of Neurology, Gerontological Research Center, Guangdong Provincial People's Hospital;2. Medical Research Center, Guangdong Provincial People's Hospital
  • Received:2008-04-16 Revised:1900-01-01 Online:2008-06-24 Published:2008-06-24

摘要: 目的 探讨尿激酶型纤溶酶原激活因子基因(PLAU)P141L多态性与中国汉族人群迟发性阿尔茨海默病(Late-onset Alzheimer'sdisease,LOAD)的关系.方法 采用DSM-Ⅳ诊断标准和NINCDS-ADRDA诊断标准中"很可能AD"的标准,选择67例LOAD患者,与71例年龄、性别与AD组匹配的健康对照者进行病例对照研究;采用聚合酶链反应限制性片段长度多态性(PCR-RFLP)技术,检测PLAU基因P141L多态性并进行关联分析.结果 LOAD组与对照组基因型分布频率均符合Hardy-Weinberg定律;两组基因型分布差异无统计学意义(χ2=0.3278,P=0.8488);两组等位基因分布差异无统计学意义(χ2=0.2238,P=0.6361).结论 PLAU基因P141L多态性与中国汉族人群LOAD未发现存在关联.

关键词: 阿尔茨海默病, 尿激酶型纤溶酶原激活因子, 基因多态性, 聚合酶链反应, 限制性片段长度多态性

Abstract: Objective To explore the relation between the P141L polymorphism of urokinase plasminogen activator gene(PLAU) and Late-onset Alzheimer's disease(LOAD) in Hans.Methods A total of 67 LOAD patients based on the diagnosis standard of DSM-Ⅳ and NINCDS-ADRDA and 71 subjects of the same age and the same sex construction as those in the case group were enrolled in this case-control study.The polymerase chain reaction-restriction fragment length polymorphism(PCR-RFLP) technique was used in detecting the polymorphism of the PLAU.Results The genotype frequencies distribution of both LOAD group and control group was in line with the Hardy-Weinberg law;No significant difference was found between the case group and the control group in terms of the genotype distribution(χ2= 0.223 8,P=0.636 1).No significant difference was found between the two groups in the distribution of allele(χ2= 0.223 8,P=0.636 1).Conclusion No relation was found between polymorphisms of PLAU and the LOAD disease in Hans.

Key words: Alzheimer disease, urokinase plasminogen activator, ! gene polymorphism, polymerase chain reaction, restriction fragment length

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