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阿尔茨海默病遗传风险:墨西哥裔、非裔和非西班牙裔美国白人中非洲裔美国人的主要风险等位基因频率及遗传结构

Alzheimer's disease genetic risk: Top African American risk allele frequencies and genetic architecture among Mexican-, African-, and non-Hispanic White Americans.

作者信息

Housini Mohammad, Zhou Zhengyang, Abdullah Lubnaa, Pathak Gita, Ayoub Reem, Gutierrez John, Andrews Shea, Phillips Nicole, O'Bryant Sid, Barber Robert

机构信息

Department of Pharmacology and Neuroscience College of Biomedical and Translational Sciences University of North Texas Health Science Center Fort Worth Texas USA.

Department of Family Medicine & Manipulative Medicine Texas College of Osteopathic Medicine University of North Texas Health Science Center Fort Worth Texas USA.

出版信息

Alzheimers Dement (N Y). 2025 Jun 19;11(2):e70124. doi: 10.1002/trc2.70124. eCollection 2025 Apr-Jun.

Abstract

INTRODUCTION

Alzheimer's disease (AD) continues to be the sixth leading cause of death in the United States. Significant efforts are spent researching etiology and potential management strategies. Although minorities face a higher disease burden and are anticipated to make up 43% of the US population by 2060, most literature on inherited AD risk has been derived from studying European ancestry. Here we evaluate frequencies of top AD risk alleles for late-onset AD (LOAD) in African- (AA), Mexican- (MA) and non-Hispanic White (NHW)-American participants enrolled in the Health & Aging Brain Study-Health Disparities (HABS-HD) cohort to determine ethnicity-specific differential genetic architecture.

METHODS

Using DNA extracted from this community-based diverse cohort ( = 3207), we calculated the genotype frequencies in each population to determine whether a significant difference is detected among the three populations. DNA genotyping was performed per manufacturer's protocols. Imputation was used for single nucleotide polymorphisms (SNPs) that were not directly genotyped. Statistical analysis was performed using R Studio.

RESULTS

Genotype frequencies for 12 out of 15 SNPs (2 apolipoprotein E [] variants, and differed significantly between groups.

DISCUSSION

This analysis expands on our previous study supporting the notion that genetic risk for AD is heterogeneous across racial and ethnic populations. Our results continue to demonstrate the valuable nature of diversity in genetic risk investigations and suggest the importance of including diverse and underrepresented racial and ethnic populations in medical research. Perhaps the most interesting finding is observed in the SNPs not found to be significantly different between groups, indicating there may be shared pleiotropic gene architecture across ethnicities.

HIGHLIGHTS

Alzheimer's disease (AD) burden is rapidly increasing in the United States; minorities are disproportionally affected.We investigate genetic health disparities in our community-based diverse cohort.Twelve of 15 evaluated single nucleotide polymorphisms significantly differ among ethnicities in the Health & Aging Brain Study-Health Disparities.

摘要

引言

阿尔茨海默病(AD)仍是美国第六大死因。人们在研究病因和潜在治疗策略方面投入了大量精力。尽管少数族裔面临更高的疾病负担,预计到2060年将占美国人口的43%,但大多数关于遗传性AD风险的文献都来自对欧洲血统人群的研究。在此,我们评估了参与健康与衰老大脑研究 - 健康差异(HABS - HD)队列的非洲裔(AA)、墨西哥裔(MA)和非西班牙裔白人(NHW)美国参与者中晚发性AD(LOAD)的主要AD风险等位基因频率,以确定种族特异性的差异遗传结构。

方法

使用从这个基于社区的多样化队列(n = 3207)中提取的DNA,我们计算了每个群体中的基因型频率,以确定在这三个群体中是否检测到显著差异。按照制造商的方案进行DNA基因分型。对未直接进行基因分型的单核苷酸多态性(SNP)进行了插补。使用R Studio进行统计分析。

结果

15个SNP中的12个(2个载脂蛋白E [ε]变体)的基因型频率在各组之间存在显著差异。

讨论

该分析扩展了我们之前的研究,支持了AD的遗传风险在不同种族和族裔人群中是异质的这一观点。我们的结果继续证明了遗传风险研究中多样性的重要性,并表明在医学研究中纳入多样化和代表性不足的种族和族裔人群的重要性。也许最有趣的发现是在未发现组间有显著差异的SNP中观察到的,这表明不同种族之间可能存在共同的多效基因结构。

要点

在美国,阿尔茨海默病(AD)负担正在迅速增加;少数族裔受到的影响尤为严重。我们在基于社区的多样化队列中研究了遗传健康差异。在健康与衰老大脑研究 - 健康差异中,15个评估的单核苷酸多态性中有12个在不同种族之间存在显著差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aaf5/12177225/6a5eef72c8b2/TRC2-11-e70124-g001.jpg

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