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越南早发性阿尔茨海默病患者的遗传学分析。

Genetic analysis of Vietnamese patients with early-onset Alzheimer's disease.

机构信息

Department of Neurology, University Medical Center, Ho Chi Minh City, Vietnam.

Medical Genetics Institute, Ho Chi Minh City, Vietnam.

出版信息

Int J Neurosci. 2022 Dec;132(12):1190-1197. doi: 10.1080/00207454.2020.1870974. Epub 2021 Feb 21.

Abstract

Alzheimer's disease (AD) is the most common type of dementia and its prevalence is rapidly increasing worldwide. Early-onset Alzheimer's disease (EOAD) constitutes of patients with age of onset earlier than 65 year-old and is known to be associated with genetic mutations. In this study, we reported the first genetic analysis of Vietnamese patients with EOAD. We analyzed targeted sequencing data obtained from a cohort of 51 Vietnamese EOAD patients to identify pathogenic variants in twenty nine well-characterized neurodengerative genes. We identified four missense mutations in genes from six individuals, which accounts for 11.8% of all tested cases. Three of these mutations were previously reported as pathogenic and one mutation in the gene was newly identified and might be specific for Vietnamese patients. Our study also found eight individuals carrying homozygous ε4 allele, the main risk factor gene for late-onset AD. Our findings showed that mutation rate in genes in Vietnamese EOAD patients is consistent with that in other ethnic groups. Although further functional studies are required to validate the pathogenesis of the new mutations, our study demonstrated the necessity of genetic screening for EOAD patients as well as additional genetic data collection in Vietnamese population.

摘要

阿尔茨海默病(AD)是最常见的痴呆症类型,其患病率在全球范围内迅速上升。早发性阿尔茨海默病(EOAD)是指发病年龄早于 65 岁的患者,已知与遗传突变有关。在这项研究中,我们报告了越南 EOAD 患者的首次遗传分析。我们分析了来自 51 名越南 EOAD 患者队列的靶向测序数据,以鉴定二十九个经过充分研究的神经退行性基因中的致病变异。我们在六名个体的 基因中发现了四个错义突变,占所有测试病例的 11.8%。其中三个突变先前被报道为致病性的,而 基因中的一个突变是新发现的,可能是越南患者特有的。我们的研究还发现了 8 名携带同源 ε4 等位基因的个体,这是晚发性 AD 的主要风险基因。我们的研究结果表明,越南 EOAD 患者中 基因的突变率与其他种族群体一致。尽管需要进一步的功能研究来验证新突变的发病机制,但我们的研究表明,对 EOAD 患者进行遗传筛查以及在越南人群中收集额外的遗传数据是必要的。

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