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APOEε4 Genotype Is Related to Brain Amyloid Among Mexican Americans in the HABS-HD Study

INTRODUCTION: Despite the fact that Hispanics are expected to experience the greatest increase in Alzheimer's disease (AD) and related dementias (ADRDs) by 2060, very little data is available regarding the fundamental biomarkers of AD among Mexican Americans who reflect the majority of Hispanic...

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Autores principales: O'Bryant, Sid E., Petersen, Melissa, Hall, James, Johnson, Leigh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245505/
https://www.ncbi.nlm.nih.gov/pubmed/35785339
http://dx.doi.org/10.3389/fneur.2022.834685
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author O'Bryant, Sid E.
Petersen, Melissa
Hall, James
Johnson, Leigh
author_facet O'Bryant, Sid E.
Petersen, Melissa
Hall, James
Johnson, Leigh
author_sort O'Bryant, Sid E.
collection PubMed
description INTRODUCTION: Despite the fact that Hispanics are expected to experience the greatest increase in Alzheimer's disease (AD) and related dementias (ADRDs) by 2060, very little data is available regarding the fundamental biomarkers of AD among Mexican Americans who reflect the majority of Hispanics in the U.S. Here we sought to examine the link between APOEε4 genotype and brain amyloid among Mexican Americans as compared to non-Hispanic white participants from the Health & Aging Brain Study – Health Disparities (HABS-HD) cohort. METHODS: PET amyloid (florbetaben) data were analyzed from 105 Mexican American and 150 non-Hispanic white participants. RESULTS: Among Mexican Americans, APOEε4 genotype presence was associated with Global SUVR (p = 0.003) as well as amyloid burden in the frontal (p < 0.001), lateral parietal (p = 0.003), lateral temporal (p = 0.008) and anterior-posterior cingulate (p = 0.005) regions of interest (ROIs). Among non-Hispanic white participants, APOEε4 genotype presence was associated with Global SUVR (p < 0.001) as well as amyloid burden in the frontal (p < 0.001), lateral parietal (p < 0.001), lateral temporal (p < 0.001) and anterior-posterior cingulate (p < 0.001) regions of interest (ROIs). The association between APOEε4 genotype and cerebral amyloid was strongest among non-Hispanic white participants. DISCUSSION/CONCLUSION: Despite the fact that the APOEε4 genotype is significantly less frequent among Mexican Americans, its presence remains to be a significant risk factor among this group for AD pathological burden across all regions. Additional work is needed to understand the presence, progression, and clinical impact of brain amyloid among Mexican Americans.
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spelling pubmed-92455052022-07-01 APOEε4 Genotype Is Related to Brain Amyloid Among Mexican Americans in the HABS-HD Study O'Bryant, Sid E. Petersen, Melissa Hall, James Johnson, Leigh Front Neurol Neurology INTRODUCTION: Despite the fact that Hispanics are expected to experience the greatest increase in Alzheimer's disease (AD) and related dementias (ADRDs) by 2060, very little data is available regarding the fundamental biomarkers of AD among Mexican Americans who reflect the majority of Hispanics in the U.S. Here we sought to examine the link between APOEε4 genotype and brain amyloid among Mexican Americans as compared to non-Hispanic white participants from the Health & Aging Brain Study – Health Disparities (HABS-HD) cohort. METHODS: PET amyloid (florbetaben) data were analyzed from 105 Mexican American and 150 non-Hispanic white participants. RESULTS: Among Mexican Americans, APOEε4 genotype presence was associated with Global SUVR (p = 0.003) as well as amyloid burden in the frontal (p < 0.001), lateral parietal (p = 0.003), lateral temporal (p = 0.008) and anterior-posterior cingulate (p = 0.005) regions of interest (ROIs). Among non-Hispanic white participants, APOEε4 genotype presence was associated with Global SUVR (p < 0.001) as well as amyloid burden in the frontal (p < 0.001), lateral parietal (p < 0.001), lateral temporal (p < 0.001) and anterior-posterior cingulate (p < 0.001) regions of interest (ROIs). The association between APOEε4 genotype and cerebral amyloid was strongest among non-Hispanic white participants. DISCUSSION/CONCLUSION: Despite the fact that the APOEε4 genotype is significantly less frequent among Mexican Americans, its presence remains to be a significant risk factor among this group for AD pathological burden across all regions. Additional work is needed to understand the presence, progression, and clinical impact of brain amyloid among Mexican Americans. Frontiers Media S.A. 2022-06-15 /pmc/articles/PMC9245505/ /pubmed/35785339 http://dx.doi.org/10.3389/fneur.2022.834685 Text en Copyright © 2022 O'Bryant, Petersen, Hall and Johnson. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
O'Bryant, Sid E.
Petersen, Melissa
Hall, James
Johnson, Leigh
APOEε4 Genotype Is Related to Brain Amyloid Among Mexican Americans in the HABS-HD Study
title APOEε4 Genotype Is Related to Brain Amyloid Among Mexican Americans in the HABS-HD Study
title_full APOEε4 Genotype Is Related to Brain Amyloid Among Mexican Americans in the HABS-HD Study
title_fullStr APOEε4 Genotype Is Related to Brain Amyloid Among Mexican Americans in the HABS-HD Study
title_full_unstemmed APOEε4 Genotype Is Related to Brain Amyloid Among Mexican Americans in the HABS-HD Study
title_short APOEε4 Genotype Is Related to Brain Amyloid Among Mexican Americans in the HABS-HD Study
title_sort apoeε4 genotype is related to brain amyloid among mexican americans in the habs-hd study
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245505/
https://www.ncbi.nlm.nih.gov/pubmed/35785339
http://dx.doi.org/10.3389/fneur.2022.834685
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