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Cerebrovascular Reactivity Across the Entire Brain in Cerebral Amyloid Angiopathy

BACKGROUND AND OBJECTIVES: Reduced cerebrovascular reactivity is proposed to be a feature of cerebral amyloid angiopathy (CAA) but has not been measured directly. Employing a global vasodilatory stimulus (hypercapnia), this study assessed the relationships between cerebrovascular reactivity and MRI...

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Autores principales: Beaudin, Andrew E., McCreary, Cheryl R., Mazerolle, Erin L., Gee, Myrlene, Sharma, Breni, Subotic, Arsenije, Zwiers, Angela M., Cox, Emily, Nelles, Krista, Charlton, Anna, Frayne, Richard, Ismail, Zahinoor, Beaulieu, Christian, Jickling, Glen C., Camicioli, Richard M., Pike, G. Bruce, Smith, Eric E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9071369/
https://www.ncbi.nlm.nih.gov/pubmed/35210294
http://dx.doi.org/10.1212/WNL.0000000000200136
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author Beaudin, Andrew E.
McCreary, Cheryl R.
Mazerolle, Erin L.
Gee, Myrlene
Sharma, Breni
Subotic, Arsenije
Zwiers, Angela M.
Cox, Emily
Nelles, Krista
Charlton, Anna
Frayne, Richard
Ismail, Zahinoor
Beaulieu, Christian
Jickling, Glen C.
Camicioli, Richard M.
Pike, G. Bruce
Smith, Eric E.
author_facet Beaudin, Andrew E.
McCreary, Cheryl R.
Mazerolle, Erin L.
Gee, Myrlene
Sharma, Breni
Subotic, Arsenije
Zwiers, Angela M.
Cox, Emily
Nelles, Krista
Charlton, Anna
Frayne, Richard
Ismail, Zahinoor
Beaulieu, Christian
Jickling, Glen C.
Camicioli, Richard M.
Pike, G. Bruce
Smith, Eric E.
author_sort Beaudin, Andrew E.
collection PubMed
description BACKGROUND AND OBJECTIVES: Reduced cerebrovascular reactivity is proposed to be a feature of cerebral amyloid angiopathy (CAA) but has not been measured directly. Employing a global vasodilatory stimulus (hypercapnia), this study assessed the relationships between cerebrovascular reactivity and MRI markers of CAA and cognitive function. METHODS: In a cross-sectional study, individuals with probable CAA, mild cognitive impairment, or dementia due to Alzheimer disease and healthy controls underwent neuropsychological testing and an MRI that included a 5% carbon dioxide challenge. Cerebrovascular reactivity was compared across groups controlling for age, sex, and the presence of hypertension, and its associations with MRI markers of CAA in participants with CAA and with cognition across all participants were determined using multivariable linear regression adjusting for group, age, sex, education, and the presence of hypertension. RESULTS: Cerebrovascular reactivity data (mean ± SD) were available for 26 participants with CAA (9 female; 74.4 ± 7.7 years), 19 participants with mild cognitive impairment (5 female; 72.1 ± 8.5 years), 12 participants with dementia due to Alzheimer disease (4 female; 69.4 ± 6.6 years), and 39 healthy controls (30 female; 68.8 ± 5.4 years). Gray and whiter matter reactivity averaged across the entire brain was lower in participants with CAA and Alzheimer disease dementia compared to healthy controls, with a predominantly posterior distribution of lower reactivity in both groups. Higher white matter hyperintensity volume was associated with lower white matter reactivity (standardized coefficient [β], 95% CI −0.48, −0.90 to −0.01). Higher gray matter reactivity was associated with better global cognitive function (β 0.19, 0.03–0.36), memory (β 0.21, 0.07–0.36), executive function (β 0.20, 0.02–0.39), and processing speed (β 0.27, 0.10–0.45) and higher white matter reactivity was associated with higher memory (β 0.22, 0.08–0.36) and processing speed (β 0.23, 0.06–0.40). CONCLUSIONS: Reduced cerebrovascular reactivity is a core feature of CAA and its assessment may provide an additional biomarker for disease severity and cognitive impairment.
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spelling pubmed-90713692022-05-06 Cerebrovascular Reactivity Across the Entire Brain in Cerebral Amyloid Angiopathy Beaudin, Andrew E. McCreary, Cheryl R. Mazerolle, Erin L. Gee, Myrlene Sharma, Breni Subotic, Arsenije Zwiers, Angela M. Cox, Emily Nelles, Krista Charlton, Anna Frayne, Richard Ismail, Zahinoor Beaulieu, Christian Jickling, Glen C. Camicioli, Richard M. Pike, G. Bruce Smith, Eric E. Neurology Research Article BACKGROUND AND OBJECTIVES: Reduced cerebrovascular reactivity is proposed to be a feature of cerebral amyloid angiopathy (CAA) but has not been measured directly. Employing a global vasodilatory stimulus (hypercapnia), this study assessed the relationships between cerebrovascular reactivity and MRI markers of CAA and cognitive function. METHODS: In a cross-sectional study, individuals with probable CAA, mild cognitive impairment, or dementia due to Alzheimer disease and healthy controls underwent neuropsychological testing and an MRI that included a 5% carbon dioxide challenge. Cerebrovascular reactivity was compared across groups controlling for age, sex, and the presence of hypertension, and its associations with MRI markers of CAA in participants with CAA and with cognition across all participants were determined using multivariable linear regression adjusting for group, age, sex, education, and the presence of hypertension. RESULTS: Cerebrovascular reactivity data (mean ± SD) were available for 26 participants with CAA (9 female; 74.4 ± 7.7 years), 19 participants with mild cognitive impairment (5 female; 72.1 ± 8.5 years), 12 participants with dementia due to Alzheimer disease (4 female; 69.4 ± 6.6 years), and 39 healthy controls (30 female; 68.8 ± 5.4 years). Gray and whiter matter reactivity averaged across the entire brain was lower in participants with CAA and Alzheimer disease dementia compared to healthy controls, with a predominantly posterior distribution of lower reactivity in both groups. Higher white matter hyperintensity volume was associated with lower white matter reactivity (standardized coefficient [β], 95% CI −0.48, −0.90 to −0.01). Higher gray matter reactivity was associated with better global cognitive function (β 0.19, 0.03–0.36), memory (β 0.21, 0.07–0.36), executive function (β 0.20, 0.02–0.39), and processing speed (β 0.27, 0.10–0.45) and higher white matter reactivity was associated with higher memory (β 0.22, 0.08–0.36) and processing speed (β 0.23, 0.06–0.40). CONCLUSIONS: Reduced cerebrovascular reactivity is a core feature of CAA and its assessment may provide an additional biomarker for disease severity and cognitive impairment. Lippincott Williams & Wilkins 2022-04-26 /pmc/articles/PMC9071369/ /pubmed/35210294 http://dx.doi.org/10.1212/WNL.0000000000200136 Text en Copyright © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Research Article
Beaudin, Andrew E.
McCreary, Cheryl R.
Mazerolle, Erin L.
Gee, Myrlene
Sharma, Breni
Subotic, Arsenije
Zwiers, Angela M.
Cox, Emily
Nelles, Krista
Charlton, Anna
Frayne, Richard
Ismail, Zahinoor
Beaulieu, Christian
Jickling, Glen C.
Camicioli, Richard M.
Pike, G. Bruce
Smith, Eric E.
Cerebrovascular Reactivity Across the Entire Brain in Cerebral Amyloid Angiopathy
title Cerebrovascular Reactivity Across the Entire Brain in Cerebral Amyloid Angiopathy
title_full Cerebrovascular Reactivity Across the Entire Brain in Cerebral Amyloid Angiopathy
title_fullStr Cerebrovascular Reactivity Across the Entire Brain in Cerebral Amyloid Angiopathy
title_full_unstemmed Cerebrovascular Reactivity Across the Entire Brain in Cerebral Amyloid Angiopathy
title_short Cerebrovascular Reactivity Across the Entire Brain in Cerebral Amyloid Angiopathy
title_sort cerebrovascular reactivity across the entire brain in cerebral amyloid angiopathy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9071369/
https://www.ncbi.nlm.nih.gov/pubmed/35210294
http://dx.doi.org/10.1212/WNL.0000000000200136
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