Title
Dissecting the role of Amerindian genetic ancestry and the ApoE ε4 allele on Alzheimer disease in an admixed Peruvian population
Date Issued
01 May 2021
Access level
open access
Resource Type
journal article
Author(s)
Marca-Ysabel M.V.
Rajabli F.
Whitehead P.G.
Hofmann N.K.
Milla Neyra A.K.
Meza Vega M.
Adams L.D.
Mena P.R.
Rosario I.
Cuccaro M.L.
Vance J.M.
Beecham G.W.
Mazzetti Soler P.E.
Pericak-Vance M.A.
Publisher(s)
Elsevier Inc.
Abstract
Alzheimer disease (AD) is the leading cause of dementia in the elderly and occurs in all ethnic and racial groups. The apolipoprotein E (ApoE) ε4 is the most significant genetic risk factor for late-onset AD and shows the strongest effect among East Asian populations followed by non-Hispanic white populations and has a relatively lower effect in African descent populations. Admixture analysis in the African American and Puerto Rican populations showed that the variation in ε4 risk is correlated with the genetic ancestral background local to the ApoE gene. Native American populations are substantially underrepresented in AD genetic studies. The Peruvian population with up to ~80 of Amerindian (AI) ancestry provides a unique opportunity to assess the role of AI ancestry in AD. In this study, we assess the effect of the ApoE ε4 allele on AD in the Peruvian population. A total of 79 AD cases and 128 unrelated cognitive healthy controls from Peruvian population were included in the study. Genome-wide genotyping was performed using the Illumina Global screening array v2.0. Global ancestry and local ancestry analyses were assessed. The effect of the ApoE ε4 allele on AD was tested using a logistic regression model by adjusting for age, gender, and population substructure (first 3 principal components). Results showed that the genetic ancestry surrounding the ApoE gene is predominantly AI (60.6%) and the ε4 allele is significantly associated with increased risk of AD in the Peruvian population (odds ratio = 5.02, confidence interval: 2.3–12.5, p-value = 2e-4). Our results showed that the risk for AD from ApoE ε4 in Peruvians is higher than we have observed in non-Hispanic white populations. Given the high admixture of AI ancestry in the Peruvian population, it suggests that the AI genetic ancestry local to the ApoE gene is contributing to a strong risk for AD in ε4 carriers. Our data also support the findings of an interaction between the genetic risk allele ApoE ε4 and the ancestral backgrounds located around the genomic region of ApoE gene.
Start page
298.e11
End page
298.e15
Volume
101
Language
English
OCDE Knowledge area
Psiquiatría
Neurología clínica
Subjects
Scopus EID
2-s2.0-85100257729
PubMed ID
Source
Neurobiology of Aging
ISSN of the container
01974580
Sponsor(s)
Research reported in this publication was supported in part by the Fogarty International Center of the National Institutes of Health and the National Institute of Neurological Disorders and Stroke under grant #D43TW009345 awarded to the Northern Pacific Global Health Fellows Program from National Institutes of Health, grant #D43TW009137 awarded to the Interdisciplinary Cerebrovascular Diseases Training Program in South America from National Institutes of Health, the AG054074 grant from the National Institutes on Aging, and the A2018556 F grant from the BrightFocus Foundation. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. We are grateful for Erik Figueroa-Ildefonso for his contribution on the logistics and support on laboratory work.
Sources of information:
Directorio de Producción Científica
Scopus