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Magnetic resonance evidence of increased iron content in subcortical brain regions in asymptomatic Alzheimer's disease

While iron over‐accumulation has been reported in late stage Alzheimer's disease (AD), whether this occurs early in the asymptomatic stage of AD remains unknown. We aimed to assess brain iron levels in asymptomatic AD using quantitative MR relaxometry of effective transverse relaxation rate (R2...

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Autores principales: Lin, Qixiang, Shahid, Salman, Hone‐Blanchet, Antoine, Huang, Shuai, Wu, Junjie, Bisht, Aditya, Loring, David, Goldstein, Felicia, Levey, Allan, Crosson, Bruce, Lah, James, Qiu, Deqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10171513/
https://www.ncbi.nlm.nih.gov/pubmed/36929676
http://dx.doi.org/10.1002/hbm.26263
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author Lin, Qixiang
Shahid, Salman
Hone‐Blanchet, Antoine
Huang, Shuai
Wu, Junjie
Bisht, Aditya
Loring, David
Goldstein, Felicia
Levey, Allan
Crosson, Bruce
Lah, James
Qiu, Deqiang
author_facet Lin, Qixiang
Shahid, Salman
Hone‐Blanchet, Antoine
Huang, Shuai
Wu, Junjie
Bisht, Aditya
Loring, David
Goldstein, Felicia
Levey, Allan
Crosson, Bruce
Lah, James
Qiu, Deqiang
author_sort Lin, Qixiang
collection PubMed
description While iron over‐accumulation has been reported in late stage Alzheimer's disease (AD), whether this occurs early in the asymptomatic stage of AD remains unknown. We aimed to assess brain iron levels in asymptomatic AD using quantitative MR relaxometry of effective transverse relaxation rate (R2*) and longitudinal relaxation rate (R1), and recruited 118 participants comprised of three groups including healthy young participants, and cognitively normal older individuals without or with positive AD biomarkers based on cerebrospinal fluid (CSF) proteomics analysis. Compared with the healthy young group, increased R2* was found in widespread cortical and subcortical regions in the older groups. Further, significantly higher levels of R2* were found in the cognitively normal older subjects with positive CSF AD biomarker (i.e., asymptomatic AD) compared with those with negative AD biomarker in subcortical regions including the left and right caudate, left and right putamen, and left and right globus pallidus (p < .05 for all regions), suggesting increased iron content in these regions. Subcortical R2* of some regions was found to significantly correlate with CSF AD biomarkers and neuropsychological assessments of visuospatial functions. In conclusion, R2* could be a valuable biomarker for studying early pathophysiological changes in AD.
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spelling pubmed-101715132023-05-11 Magnetic resonance evidence of increased iron content in subcortical brain regions in asymptomatic Alzheimer's disease Lin, Qixiang Shahid, Salman Hone‐Blanchet, Antoine Huang, Shuai Wu, Junjie Bisht, Aditya Loring, David Goldstein, Felicia Levey, Allan Crosson, Bruce Lah, James Qiu, Deqiang Hum Brain Mapp Research Articles While iron over‐accumulation has been reported in late stage Alzheimer's disease (AD), whether this occurs early in the asymptomatic stage of AD remains unknown. We aimed to assess brain iron levels in asymptomatic AD using quantitative MR relaxometry of effective transverse relaxation rate (R2*) and longitudinal relaxation rate (R1), and recruited 118 participants comprised of three groups including healthy young participants, and cognitively normal older individuals without or with positive AD biomarkers based on cerebrospinal fluid (CSF) proteomics analysis. Compared with the healthy young group, increased R2* was found in widespread cortical and subcortical regions in the older groups. Further, significantly higher levels of R2* were found in the cognitively normal older subjects with positive CSF AD biomarker (i.e., asymptomatic AD) compared with those with negative AD biomarker in subcortical regions including the left and right caudate, left and right putamen, and left and right globus pallidus (p < .05 for all regions), suggesting increased iron content in these regions. Subcortical R2* of some regions was found to significantly correlate with CSF AD biomarkers and neuropsychological assessments of visuospatial functions. In conclusion, R2* could be a valuable biomarker for studying early pathophysiological changes in AD. John Wiley & Sons, Inc. 2023-03-16 /pmc/articles/PMC10171513/ /pubmed/36929676 http://dx.doi.org/10.1002/hbm.26263 Text en © 2023 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research Articles
Lin, Qixiang
Shahid, Salman
Hone‐Blanchet, Antoine
Huang, Shuai
Wu, Junjie
Bisht, Aditya
Loring, David
Goldstein, Felicia
Levey, Allan
Crosson, Bruce
Lah, James
Qiu, Deqiang
Magnetic resonance evidence of increased iron content in subcortical brain regions in asymptomatic Alzheimer's disease
title Magnetic resonance evidence of increased iron content in subcortical brain regions in asymptomatic Alzheimer's disease
title_full Magnetic resonance evidence of increased iron content in subcortical brain regions in asymptomatic Alzheimer's disease
title_fullStr Magnetic resonance evidence of increased iron content in subcortical brain regions in asymptomatic Alzheimer's disease
title_full_unstemmed Magnetic resonance evidence of increased iron content in subcortical brain regions in asymptomatic Alzheimer's disease
title_short Magnetic resonance evidence of increased iron content in subcortical brain regions in asymptomatic Alzheimer's disease
title_sort magnetic resonance evidence of increased iron content in subcortical brain regions in asymptomatic alzheimer's disease
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10171513/
https://www.ncbi.nlm.nih.gov/pubmed/36929676
http://dx.doi.org/10.1002/hbm.26263
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