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Depression is differentially related to cognitive and biomarker outcomes among Mexican Americans

INTRODUCTION: Despite tremendous advancements in the research of Alzheimer’s disease (AD), Mexican Americans, who reflect 65% of the US Hispanic community, remain severely underrepresented in research. Our data demonstrate that risk factors for, and biomarkers of, AD are different among Mexican Amer...

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Autores principales: O’Bryant, Sid E., Petersen, Melissa, Hall, James, Johnson, Leigh A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9445986/
https://www.ncbi.nlm.nih.gov/pubmed/36081458
http://dx.doi.org/10.3389/fpsyt.2022.901403
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author O’Bryant, Sid E.
Petersen, Melissa
Hall, James
Johnson, Leigh A.
author_facet O’Bryant, Sid E.
Petersen, Melissa
Hall, James
Johnson, Leigh A.
author_sort O’Bryant, Sid E.
collection PubMed
description INTRODUCTION: Despite tremendous advancements in the research of Alzheimer’s disease (AD), Mexican Americans, who reflect 65% of the US Hispanic community, remain severely underrepresented in research. Our data demonstrate that risk factors for, and biomarkers of, AD are different among Mexican Americans as compared with non-Hispanic whites. Here, we examined the impact of depressive symptoms on cognitive and AD-relevant biomarker outcomes among the Mexican Americans. METHODS: Data were examined from 1,633 (852 Mexican Americans and 781 non-Hispanic whites) of the Health and Aging Brain Study–Health Disparities (HABS–HD). Depression was assessed using the Geriatric Depression Scale while cognition was measured using detailed neuropsychological testing. Plasma biomarkers of Aβ40, Aβ42, total tau, and NfL were examined in addition to MRI-based neurodegeneration. PET amyloid data were available in a subset of participants. RESULTS: Depressive symptoms were significantly associated with cognitive testing results among both Mexican Americans and non-Hispanic whites. However, depression was only significantly associated with cognitive outcomes and plasma biomarkers among the Mexican American APOEε4 non-carriers. DISCUSSION: Depressive symptoms are more commonly endorsed by Mexican Americans and these symptoms are more strongly associated with cognitive and AD-biomarker outcomes among this ethnic group. However, depression scores were only related to AD outcomes among APOEε4 non-carriers within the Mexican American group. These findings can aid in the development of a population-informed precision medicine for treating and preventing cognitive loss among the Mexican Americans.
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spelling pubmed-94459862022-09-07 Depression is differentially related to cognitive and biomarker outcomes among Mexican Americans O’Bryant, Sid E. Petersen, Melissa Hall, James Johnson, Leigh A. Front Psychiatry Psychiatry INTRODUCTION: Despite tremendous advancements in the research of Alzheimer’s disease (AD), Mexican Americans, who reflect 65% of the US Hispanic community, remain severely underrepresented in research. Our data demonstrate that risk factors for, and biomarkers of, AD are different among Mexican Americans as compared with non-Hispanic whites. Here, we examined the impact of depressive symptoms on cognitive and AD-relevant biomarker outcomes among the Mexican Americans. METHODS: Data were examined from 1,633 (852 Mexican Americans and 781 non-Hispanic whites) of the Health and Aging Brain Study–Health Disparities (HABS–HD). Depression was assessed using the Geriatric Depression Scale while cognition was measured using detailed neuropsychological testing. Plasma biomarkers of Aβ40, Aβ42, total tau, and NfL were examined in addition to MRI-based neurodegeneration. PET amyloid data were available in a subset of participants. RESULTS: Depressive symptoms were significantly associated with cognitive testing results among both Mexican Americans and non-Hispanic whites. However, depression was only significantly associated with cognitive outcomes and plasma biomarkers among the Mexican American APOEε4 non-carriers. DISCUSSION: Depressive symptoms are more commonly endorsed by Mexican Americans and these symptoms are more strongly associated with cognitive and AD-biomarker outcomes among this ethnic group. However, depression scores were only related to AD outcomes among APOEε4 non-carriers within the Mexican American group. These findings can aid in the development of a population-informed precision medicine for treating and preventing cognitive loss among the Mexican Americans. Frontiers Media S.A. 2022-08-23 /pmc/articles/PMC9445986/ /pubmed/36081458 http://dx.doi.org/10.3389/fpsyt.2022.901403 Text en Copyright © 2022 O’Bryant, Petersen, Hall, Johnson and HABS-HD Study Team. 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 Psychiatry
O’Bryant, Sid E.
Petersen, Melissa
Hall, James
Johnson, Leigh A.
Depression is differentially related to cognitive and biomarker outcomes among Mexican Americans
title Depression is differentially related to cognitive and biomarker outcomes among Mexican Americans
title_full Depression is differentially related to cognitive and biomarker outcomes among Mexican Americans
title_fullStr Depression is differentially related to cognitive and biomarker outcomes among Mexican Americans
title_full_unstemmed Depression is differentially related to cognitive and biomarker outcomes among Mexican Americans
title_short Depression is differentially related to cognitive and biomarker outcomes among Mexican Americans
title_sort depression is differentially related to cognitive and biomarker outcomes among mexican americans
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9445986/
https://www.ncbi.nlm.nih.gov/pubmed/36081458
http://dx.doi.org/10.3389/fpsyt.2022.901403
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