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Brain iron content in cerebral amyloid angiopathy using quantitative susceptibility mapping

INTRODUCTION: Cerebral amyloid angiopathy (CAA) is a small vessel disease that causes covert and symptomatic brain hemorrhaging. We hypothesized that persons with CAA would have increased brain iron content detectable by quantitative susceptibility mapping (QSM) on magnetic resonance imaging (MRI),...

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Autores principales: Sharma, Breni, Beaudin, Andrew E., Cox, Emily, Saad, Feryal, Nelles, Krista, Gee, Myrlene, Frayne, Richard, Gobbi, David G., Camicioli, Richard, Smith, Eric E., McCreary, Cheryl R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10149796/
https://www.ncbi.nlm.nih.gov/pubmed/37139529
http://dx.doi.org/10.3389/fnins.2023.1139988
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author Sharma, Breni
Beaudin, Andrew E.
Cox, Emily
Saad, Feryal
Nelles, Krista
Gee, Myrlene
Frayne, Richard
Gobbi, David G.
Camicioli, Richard
Smith, Eric E.
McCreary, Cheryl R.
author_facet Sharma, Breni
Beaudin, Andrew E.
Cox, Emily
Saad, Feryal
Nelles, Krista
Gee, Myrlene
Frayne, Richard
Gobbi, David G.
Camicioli, Richard
Smith, Eric E.
McCreary, Cheryl R.
author_sort Sharma, Breni
collection PubMed
description INTRODUCTION: Cerebral amyloid angiopathy (CAA) is a small vessel disease that causes covert and symptomatic brain hemorrhaging. We hypothesized that persons with CAA would have increased brain iron content detectable by quantitative susceptibility mapping (QSM) on magnetic resonance imaging (MRI), and that higher iron content would be associated with worse cognition. METHODS: Participants with CAA (n = 21), mild Alzheimer’s disease with dementia (AD-dementia; n = 14), and normal controls (NC; n = 83) underwent 3T MRI. Post-processing QSM techniques were applied to obtain susceptibility values for regions of the frontal and occipital lobe, thalamus, caudate, putamen, pallidum, and hippocampus. Linear regression was used to examine differences between groups, and associations with global cognition, controlling for multiple comparisons using the false discovery rate method. RESULTS: No differences were found between regions of interest in CAA compared to NC. In AD, the calcarine sulcus had greater iron than NC (β = 0.99 [95% CI: 0.44, 1.53], q < 0.01). However, calcarine sulcus iron content was not associated with global cognition, measured by the Montreal Cognitive Assessment (p > 0.05 for all participants, NC, CAA, and AD). DISCUSSION: After correcting for multiple comparisons, brain iron content, measured via QSM, was not elevated in CAA compared to NC in this exploratory study.
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spelling pubmed-101497962023-05-02 Brain iron content in cerebral amyloid angiopathy using quantitative susceptibility mapping Sharma, Breni Beaudin, Andrew E. Cox, Emily Saad, Feryal Nelles, Krista Gee, Myrlene Frayne, Richard Gobbi, David G. Camicioli, Richard Smith, Eric E. McCreary, Cheryl R. Front Neurosci Neuroscience INTRODUCTION: Cerebral amyloid angiopathy (CAA) is a small vessel disease that causes covert and symptomatic brain hemorrhaging. We hypothesized that persons with CAA would have increased brain iron content detectable by quantitative susceptibility mapping (QSM) on magnetic resonance imaging (MRI), and that higher iron content would be associated with worse cognition. METHODS: Participants with CAA (n = 21), mild Alzheimer’s disease with dementia (AD-dementia; n = 14), and normal controls (NC; n = 83) underwent 3T MRI. Post-processing QSM techniques were applied to obtain susceptibility values for regions of the frontal and occipital lobe, thalamus, caudate, putamen, pallidum, and hippocampus. Linear regression was used to examine differences between groups, and associations with global cognition, controlling for multiple comparisons using the false discovery rate method. RESULTS: No differences were found between regions of interest in CAA compared to NC. In AD, the calcarine sulcus had greater iron than NC (β = 0.99 [95% CI: 0.44, 1.53], q < 0.01). However, calcarine sulcus iron content was not associated with global cognition, measured by the Montreal Cognitive Assessment (p > 0.05 for all participants, NC, CAA, and AD). DISCUSSION: After correcting for multiple comparisons, brain iron content, measured via QSM, was not elevated in CAA compared to NC in this exploratory study. Frontiers Media S.A. 2023-04-17 /pmc/articles/PMC10149796/ /pubmed/37139529 http://dx.doi.org/10.3389/fnins.2023.1139988 Text en Copyright © 2023 Sharma, Beaudin, Cox, Saad, Nelles, Gee, Frayne, Gobbi, Camicioli, Smith and McCreary. 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 Neuroscience
Sharma, Breni
Beaudin, Andrew E.
Cox, Emily
Saad, Feryal
Nelles, Krista
Gee, Myrlene
Frayne, Richard
Gobbi, David G.
Camicioli, Richard
Smith, Eric E.
McCreary, Cheryl R.
Brain iron content in cerebral amyloid angiopathy using quantitative susceptibility mapping
title Brain iron content in cerebral amyloid angiopathy using quantitative susceptibility mapping
title_full Brain iron content in cerebral amyloid angiopathy using quantitative susceptibility mapping
title_fullStr Brain iron content in cerebral amyloid angiopathy using quantitative susceptibility mapping
title_full_unstemmed Brain iron content in cerebral amyloid angiopathy using quantitative susceptibility mapping
title_short Brain iron content in cerebral amyloid angiopathy using quantitative susceptibility mapping
title_sort brain iron content in cerebral amyloid angiopathy using quantitative susceptibility mapping
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10149796/
https://www.ncbi.nlm.nih.gov/pubmed/37139529
http://dx.doi.org/10.3389/fnins.2023.1139988
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