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载脂蛋白E、白细胞介素-1α基因多态性与成都地区阿尔茨海默病的关联分析
引用本文:唐牟尼,张振馨,韩海英,刘协和,沈岩.载脂蛋白E、白细胞介素-1α基因多态性与成都地区阿尔茨海默病的关联分析[J].中华医学遗传学杂志,2004,21(2):176-178.
作者姓名:唐牟尼  张振馨  韩海英  刘协和  沈岩
作者单位:1. 510370,广州市脑科医院老年科
2. 100730,北京,中国医学科学院中国协和医科大学北京协和医院神经内科
3. 广州市脑科医院老年科
4. 四川大学华西医院精神科
5. 100730,北京,中国医学科学院中国协和医科大学北京协和医院基础医学研究所生化室
基金项目:纽约中华医学基金会基金 (99- 699)~~
摘    要:目的 探讨载脂蛋白E(apolipoprotein E,APOE)和白细胞介素 - 1α(interleukin- 1α,IL- 1α)基因多态性与成都地区阿尔茨海默病 (Alzheimer's disease,AD)的关系。方法 用聚合酶链反应 -限制性片段长度多态性技术检测成都地区流行病学调查中诊断为 AD的 114例患者和 113名健康老年人 APOE基因和 IL - 1α基因多态性。结果 中度、重度 AD组含 APOEε4基因型频率 (2 8.6 % )显著高于轻度 AD组 (18.5 % )和正常对照组 (14 .2 % ) ,其中中度、重度 AD组与正常对照组差异有显著性 (OR=2 .4 ,95 % CI:1.1~5 .5 )。将ε4等位基因频率与ε2和ε3等位基因频率之和比较 ,中度、重度 AD组与正常对照组的差异有显著性 (OR=2 .6 ,95 % CI:1.3~ 5 .3)。 AD患者组和正常对照组 IL - 1α基因型和等位基因频率分布相似 ,差异无显著性 (P>0 .0 5 )。结论  APOEε4等位基因与中、重度 AD相关联 ,是中、重度 AD的易感因素。 IL - 1α基因多态性与中国成都地区 AD患者无关联。

关 键 词:阿尔茨海默病  载脂蛋白E  白细胞介素-1α
修稿时间:2003年4月21日

Analysis on association between the polymorphisms in apolipoprotein E, interleukin-1α genes and Alzheimer's disease in Chengdu area
TANG Mu-ni,ZHANG Zhen-xin,HAN Hai-ying,LIU Xie-he,SHEN Yan..Analysis on association between the polymorphisms in apolipoprotein E, interleukin-1α genes and Alzheimer''s disease in Chengdu area[J].Chinese Journal of Medical Genetics,2004,21(2):176-178.
Authors:TANG Mu-ni  ZHANG Zhen-xin  HAN Hai-ying  LIU Xie-he  SHEN Yan
Institution:Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, 100730 PR China. tangmuni@hotmail.com
Abstract:OBJECTIVE: To investigate the correlation between the polymorphisms of apolipoprotein E(APOE), the interleukin-1 alpha (IL-1 alpha ) genes and the susceptibility to Alzheimer's disease(AD). METHODS: Association study was performed in 114 AD patients and 113 healthy elderly individuals from Chengdu, China. Polymorphisms of APOE and IL-1 alpha genes were analyzed with polymerase chain reaction-restriction fragment length polymorphism. RESULTS: The frequency of APOE-epsilon 4-carrying genotype in moderate to severe AD patients (28.6%) was higher than that of mild patients (18.5%) and the controls (14.2%), and the difference between moderate to severe AD group and the control group was significant (OR=2.4, 95%CI: 1.1-5.5). The frequency of epsilon 4 was also of significant difference between the group of moderate to severe dementia and the control group (OR=2.6, 95%CI: 1.3-5.3). However, no significant difference in distribution of IL-1 alpha polymorphism between AD patients and controls was observed. CONCLUSION: The APOE epsilon 4 allele was associated with moderate to severe AD while no association between the IL-1 alpha gene polymorphism and AD was found.
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