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Polymorphism of apolipoproteine E in relation with Alzheimer and vascular dementia.

机译:载脂蛋白E的多态性与阿尔茨海默氏症和血管性痴呆有关。

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1. The epsilon 4 allele of the apolipoprotein E gene increases the risk of late onset familial and sporadic Alzheimer disease. Relation of epsilon 4 allele of the apolipoprotein E gene to various types of dementia and the onset of dementia were analyzed in the present study. 2. The study comprised 139 patients (50 men and 89 women) with dementia, mean age 73.61 years (range 47-98). The diagnosis of dementia was made according to Diagnostic and Statistical Manual of Mental Disorders, and subtypes diagnoses were made according to NINCDS-ADRDA and NINDS-AIREN criteria. Minimental State Examination (MMSE) was used for the screening of dementia. Apolipoprotein E polymorphism was determined by the PCR-RFLP technique-polymerase chain reaction and subsequent digestion with specific restriction endonuclease. For statistical analyses chi-square test and the crude Gart s odds ratio (OR) and 95% confidence intervals (CI) were used. 3. From 139 dementia patients (MMSE < or =24 points) in 61 (45%) Alzheimer disease (AD) was present, in 44 patients (31%) vascular dementia (VD), and in 34 (24%) mixed dementia (MD) were revealed. In comparison with control group the presence of at least one ApoE-varepsilon4 allele was significantly higher only in the group with AD (p < 0.001), (OR=2.76; 95%: 1.42-5.36). The frequency of epsilon4 allele carriers was significantly overrepresented in AD group compared with VD (chi(2)=5.94; p=0.0148). Differences between AD and MD or VD and MD were not confirmed.
机译:1.载脂蛋白E基因的epsilon 4等位基因增加了晚期家族性和偶发性阿尔茨海默氏病的风险。本研究分析了载脂蛋白E基因的epsilon 4等位基因与各种类型痴呆和痴呆发作的关系。 2.该研究包括139名痴呆患者(50名男性和89名女性),平均年龄73.61岁(范围47-98)。痴呆症的诊断根据《精神疾病诊断和统计手册》进行,亚型诊断根据NINCDS-ADRDA和NINDS-AIREN标准进行。进行了国家状态检查(MMSE)筛查痴呆症。通过PCR-RFLP技术-聚合酶链反应和随后用特异性限制性核酸内切酶消化来确定载脂蛋白E多态性。为了进行统计分析,使用了卡方检验和原始的Gart比值比(OR)和95%的置信区间(CI)。 3.在139名痴呆患者(MMSE <或= 24分)中,有61名(45%)阿尔茨海默病(AD),44名患者(31%),血管性痴呆(VD)和34名(24%)混合型痴呆(MD)被发现。与对照组相比,至少一个ApoE-varepsilon4等位基因的存在仅在AD组显着更高(p <0.001)(OR = 2.76; 95%:1.42-5.36)。与VD相比,AD组中epsilon4等位基因携带者的频率明显过高(chi(2)= 5.94; p = 0.0148)。未确认AD与MD或VD与MD之间的差异。

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