Katalog Plus
Bibliothek der Frankfurt UAS
Bald neuer Katalog: sichern Sie sich schon vorab Ihre persönlichen Merklisten im Nutzerkonto: Anleitung.
Dieses Ergebnis aus BASE kann Gästen nicht angezeigt werden.  Login für vollen Zugriff.

A locus at 19q13.31 significantly reduces the ApoE ε4 risk for Alzheimer's Disease in African Ancestry

Title: A locus at 19q13.31 significantly reduces the ApoE ε4 risk for Alzheimer's Disease in African Ancestry
Authors: Rajabli F; Beecham GW; Hendrie HC; Baiyewu O; Ogunniyi A; Gao S; Kushch NA; Lipkin-Vasquez M; Hamilton-Nelson KL; Young JI; Dykxhoorn DM; Nuytemans K; Kunkle BW; Wang L; Jin F; Liu X; Feliciano-Astacio BE; Alzheimer's Disease Sequencing Project AsDGC; Schellenberg GD; Dalgard CL; Griswold AJ; Byrd GS; Reitz C; Cuccaro ML; Haines JL; Pericak-Vance MA; Vance JM
Source: PLoS Genetics, 5 July 2022
Publisher Information: Public Library of Science
Publication Year: 2022
Collection: Newcastle University Library ePrints Service
Description: Copyright: © 2022 Rajabli et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. African descent populations have a lower Alzheimer disease risk from ApoE ε4 compared to other populations. Ancestry analysis showed that the difference in risk between African and European populations lies in the ancestral genomic background surrounding the ApoE locus (local ancestry). Identifying the mechanism(s) of this protection could lead to greater insight into the etiology of Alzheimer disease and more personalized therapeutic intervention. Our objective is to follow up the local ancestry finding and identify the genetic variants that drive this risk difference and result in a lower risk for developing Alzheimer disease in African ancestry populations. We performed association analyses using a logistic regression model with the ApoE ε4 allele as an interaction term and adjusted for genome-wide ancestry, age, and sex. Discovery analysis included imputed SNP data of 1,850 Alzheimer disease and 4,331 cognitively intact African American individuals. We performed replication analyses on 63 whole genome sequenced Alzheimer disease and 648 cognitively intact Ibadan individuals. Additionally, we reproduced results using whole-genome sequencing of 273 Alzheimer disease and 275 cognitively intact admixed Puerto Rican individuals. A further comparison was done with SNP imputation from an additional 8,463 Alzheimer disease and 11,365 cognitively intact non-Hispanic White individuals. We identified a significant interaction between the ApoE ε4 allele and the SNP rs10423769_A allele, (β = -0.54,SE = 0.12,p-value = 7.50x10-6) in the discovery data set, and replicated this finding in Ibadan (β = -1.32,SE = 0.52,p-value = 1.15x10-2) and Puerto Rican (β = -1.27,SE = 0.64,p-value = 4.91x10-2) individuals. The non-Hispanic Whites analyses showed an interaction ...
Document Type: article in journal/newspaper
File Description: application/pdf
Language: unknown
Relation: https://eprints.ncl.ac.uk/297240; https://eprints.ncl.ac.uk/fulltext.aspx?url=297240/76283553-5139-4C60-AD86-5684E8F1200A.pdf&pub_id=297240
Availability: https://eprints.ncl.ac.uk/297240
Rights: https://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.AE55A5C7
Database: BASE