Correlation of R219K polymorphism of ABCA1 gene and the risk of Alzheimer's disease in the southwest of Iran

IF 0.8 Q4 GENETICS & HEREDITY Meta Gene Pub Date : 2021-12-01 DOI:10.1016/j.mgene.2021.100961
Ashraf Sepiani , Maryam Cheraghzadeh , Zahra Nazeri , Shirin Azizidoost , Bita Shalbafan , Alireza Kheirollah
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Abstract

Introduction

Alzheimer's disease (AD), as a neurodegenerative disease, is the most common reason for dementia in the elderly. ATP- binding cassette transporter 1 (ABCA1) is a cell membrane transporter protein which is involved in cholesterol efflux. The aim of this study is to evaluate the correlation between polymorphisms of G/A (rs2230806) in ABCA1 gene with sporadic Alzheimer's disease in the southwest of Iran.

Methods

This case-control study was conducted in 180 subjects, including 100 sporadic AD patients and 80 healthy subjects. Genotypes of all samples were determined using the PCR–restriction fragment length polymorphism (PCR–RFLP) technique.

Results

The analysis of the R219K Polymorphism of ABCA1 gene indicated that there was no significant distinction between AD patients and controls. In this study when groups were stratified by age and sex, results showed that in the control group with less than 75 years, the risk of developing AD was significantly lower than subjects who were older than 75 years (P = 0.019, OR = 0.46, 95% CI = 0.24–0.88). A significant difference was detected in the risk of AD between patient and control in females older than 75 years (P = 0.028).

Conclusion

The results of this study confirm that aging is an important risk factor for AD. Also, it has been found that AD is more prevalent in women compared to men. However, our results do not support the hypothesis that R219K polymorphism in the rs2230806 region of the ABCA1 as a genetic risk factor for developing AD in our study population.

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伊朗西南部地区ABCA1基因R219K多态性与阿尔茨海默病风险的相关性
阿尔茨海默病(AD)作为一种神经退行性疾病,是老年人痴呆最常见的原因。ATP结合盒转运蛋白1 (ABCA1)是一种参与胆固醇外排的细胞膜转运蛋白。本研究的目的是评估ABCA1基因G/A (rs2230806)多态性与伊朗西南部散发性阿尔茨海默病的相关性。方法采用病例对照研究180例,其中散发性AD患者100例,健康人80例。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)技术测定所有样品的基因型。结果ABCA1基因R219K多态性分析显示AD患者与对照组无显著差异。在本研究中,按年龄和性别进行分组,结果显示,年龄小于75 岁的对照组患AD的风险显著低于年龄大于75 岁的对照组(P = 0.019,OR = 0.46,95% CI = 0.24-0.88)。年龄大于75 岁的女性患AD的风险与对照组有显著差异(P = 0.028)。结论本研究结果证实年龄是AD的重要危险因素。此外,研究发现,与男性相比,AD在女性中更为普遍。然而,我们的研究结果并不支持ABCA1 rs2230806区域R219K多态性是我们研究人群中发生AD的遗传危险因素的假设。
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来源期刊
Meta Gene
Meta Gene Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
1.10
自引率
0.00%
发文量
20
期刊介绍: Meta Gene publishes meta-analysis, polymorphism and population study papers that are relevant to both human and non-human species. Examples include but are not limited to: (Relevant to human specimens): 1Meta-Analysis Papers - statistical reviews of the published literature of human genetic variation (typically linked to medical conditionals and/or congenital diseases) 2Genome Wide Association Studies (GWAS) - examination of large patient cohorts to identify common genetic factors that influence health and disease 3Human Genetics Papers - original studies describing new data on genetic variation in smaller patient populations 4Genetic Case Reports - short communications describing novel and in formative genetic mutations or chromosomal aberrations (e.g., probands) in very small demographic groups (e.g., family or unique ethnic group). (Relevant to non-human specimens): 1Small Genome Papers - Analysis of genetic variation in organelle genomes (e.g., mitochondrial DNA) 2Microbiota Papers - Analysis of microbiological variation through analysis of DNA sequencing in different biological environments 3Ecological Diversity Papers - Geographical distribution of genetic diversity of zoological or botanical species.
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