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载脂蛋白 E 多态性在不同委内瑞拉人群中 60 岁以上轻度认知障碍和阿尔茨海默病患者中的研究

Apolipoprotein E polymorphisms in adults over 60 years of age with mild cognitive impairment and Alzheimer’s disease in different Venezuelan populations.

机构信息

Facultad de Farmacia, Universidad Central de Venezuela, Caracas, Venezuela.

Instituto de Medicina Experimental, Facultad de Medicina, Universidad Central de Venezuela, Caracas, Venezuela.

出版信息

Biomedica. 2022 May 1;42(Sp. 1):116-129. doi: 10.7705/biomedica.5889.

Abstract

Introduction: Alzheimer’s disease represents a serious public health problem that tends to worsen over time. Among the most important genetic predisposing factors is the presence of the ε4 allele of the apoprotein E gene (APOE). Objective: To determine the allelic and genotypic frequencies of the APOE isoforms in adults over 60 years old with mild cognitive impairment and Alzheimer’s disease in Gran Caracas and in the indigenous Pemón community of the Kamarata-Kanaimö area, Bolívar State. Materials and methods: We studied 267 patients: 96 controls, 40 with mild cognitive impairment, 108 with Alzheimer’s from Caracas, and 23 individuals from Kamarata-Kanaimö. The APOE isoforms were determined with the AP1210Z: Seeplex® ApoE Genotyping kit. Results: The allele ε4 showed a significant association with mild cognitive impairment (OR=5.03; 95% CI: 0.98-25.70) and EA (OR=5.78; 95% CI: 1.24-26.85). The genotype frequencies for the control and mild cognitive impairment groups were ε3/ε3> ε3/ε4> ε2/ε4> ε3/ε2> ε4/ε4, and for the Alzheimer’s group, ε3/ε3> ε3/ε4> ε4/ε4> ε2/ε4> ε3/ε2 In Kamarata-Kanaimö, the order was ε3/ε3> ε3/ε4> ε4/ε4; the allele ε2 was not found in this group. Conclusions: APOE allelic and genotypic frequencies in our sample showed a similar distribution to those found in other studies in Venezuela and the Americas. The absence of the ε2 allele in the indigenous community of Kamarata-Kanaimö warrants further investigation. The positive association of the ε4 allele with both Alzheimer’s and mild cognitive impairment was reinforced. The early determination of the ε4 allele carriers can help establish preventive measures in our population.

摘要

简介

阿尔茨海默病是一个严重的公共卫生问题,且随着时间的推移病情往往会恶化。最重要的遗传易患因素之一是载脂蛋白 E 基因(APOE)的 ε4 等位基因。目的:确定在大加拉加斯和玻利瓦尔州卡马拉塔-卡纳莫地区的皮曼土著社区中,60 岁以上患有轻度认知障碍和阿尔茨海默病的成年人中 APOE 同种型的等位基因和基因型频率。材料和方法:我们研究了 267 名患者:96 名对照者、40 名轻度认知障碍患者、108 名来自加拉加斯的阿尔茨海默病患者和 23 名来自卡马拉塔-卡纳莫的个体。APOE 同种型是使用 AP1210Z:Seeplex® ApoE 基因分型试剂盒确定的。结果:等位基因 ε4 与轻度认知障碍(OR=5.03;95%CI:0.98-25.70)和 EA(OR=5.78;95%CI:1.24-26.85)显著相关。对照组和轻度认知障碍组的基因型频率为 ε3/ε3>ε3/ε4>ε2/ε4>ε3/ε2>ε4/ε4,而阿尔茨海默病组的频率为 ε3/ε3>ε3/ε4>ε4/ε4>ε2/ε4>ε3/ε2。在卡马拉塔-卡纳莫,顺序为 ε3/ε3>ε3/ε4>ε4/ε4;在这个群体中没有发现 ε2 等位基因。结论:我们样本中的 APOE 等位基因和基因型频率与委内瑞拉和美洲其他研究中的发现相似。在卡马拉塔-卡纳莫的土著社区中没有发现 ε2 等位基因,这值得进一步研究。ε4 等位基因与阿尔茨海默病和轻度认知障碍均呈正相关。早期确定 ε4 等位基因携带者有助于在我们的人群中制定预防措施。

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