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厄瓜多尔梅斯蒂索人群中APOE 4等位基因与晚发性阿尔茨海默病之间的关联。

Association between the APOE 4 Allele and Late-Onset Alzheimer's Disease in an Ecuadorian Mestizo Population.

作者信息

Montufar Stefany, Calero Cristian, Vinueza Rodrigo, Correa Patricio, Carrera-Gonzalez Andrea, Villegas Franklin, Moreta Germania, Paredes Rosario

机构信息

Hospital de Especialidades FFAA, Quito, Pichincha, Ecuador.

Hospital Carlos Andrade Marín, Quito, Pichincha, Ecuador.

出版信息

Int J Alzheimers Dis. 2017;2017:1059678. doi: 10.1155/2017/1059678. Epub 2017 Dec 4.

Abstract

Alzheimer's disease (AD) is the most common neurodegenerative disease. It has two main pathological hallmarks: amyloid plaques and neurofibrillary tangles. The APOE 4 allele has been recognized as the strongest genetic risk factor for late-onset Alzheimer's disease (LOAD) in several populations worldwide, yet the risk varies by region and ethnicity. The aims of this study were to describe APOE allele and genotype frequencies and examine the relationship between the APOE 4 allele and LOAD risk in an Ecuadorian Mestizo population. We carried out a case-control study comprising 56 individuals clinically diagnosed with probable AD (≥65 years of age) and 58 unrelated healthy control subjects (≥65 years of age). Genotyping was performed using the real-time PCR method. Our data showed that allelic and genotypic frequencies follow the trends observed in most worldwide populations. We also found a high-risk association between APOE 4 allele carriers and LOAD (OR = 7.286; 95% CI = 2.824-18.799; < 0.001). Therefore, we concluded that APOE 4 must be considered an important genetic risk factor for LOAD in the Ecuadorian Mestizo population. Additionally, we suggest that in mixed populations the effects of admixture and ethnic identity should be differentiated when evaluating genetic contributions to Alzheimer's disease risk.

摘要

阿尔茨海默病(AD)是最常见的神经退行性疾病。它有两个主要的病理特征:淀粉样斑块和神经原纤维缠结。在全球多个群体中,APOE 4等位基因已被公认为晚发性阿尔茨海默病(LOAD)最强的遗传危险因素,但风险因地区和种族而异。本研究的目的是描述厄瓜多尔梅斯蒂索人群中APOE等位基因和基因型频率,并研究APOE 4等位基因与LOAD风险之间的关系。我们进行了一项病例对照研究,包括56例临床诊断为可能患有AD(≥65岁)的个体和58例无亲缘关系的健康对照者(≥65岁)。采用实时PCR方法进行基因分型。我们的数据表明,等位基因和基因型频率遵循在世界大多数人群中观察到的趋势。我们还发现APOE 4等位基因携带者与LOAD之间存在高风险关联(OR = 7.286;95%CI = 2.824 - 18.799;< 0.001)。因此,我们得出结论,在厄瓜多尔梅斯蒂索人群中,APOE 4必须被视为LOAD的一个重要遗传危险因素。此外,我们建议在混合人群中,评估阿尔茨海默病风险的遗传贡献时,应区分混合和种族身份的影响。

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