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Cerebral amyloid angiopathy is associated with decreased functional brain connectivity

Cerebral amyloid angiopathy (CAA) is a major cause of intracerebral hemorrhage and neurological decline in the elderly. CAA results in focal brain lesions, but the influence on global brain functioning needs further investigation. Here we study functional brain connectivity in patients with Dutch ty...

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Autores principales: Drenth, Nadieh, van der Grond, Jeroen, Rombouts, Serge A.R.B., van Buchem, Mark A., Terwindt, Gisela M., Wermer, Marieke J.H., Chhatwal, Jasmeer P., Gurol, M. Edip, Greenberg, Steven M., van Rooden, Sanneke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806879/
https://www.ncbi.nlm.nih.gov/pubmed/33421870
http://dx.doi.org/10.1016/j.nicl.2020.102546
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author Drenth, Nadieh
van der Grond, Jeroen
Rombouts, Serge A.R.B.
van Buchem, Mark A.
Terwindt, Gisela M.
Wermer, Marieke J.H.
Chhatwal, Jasmeer P.
Gurol, M. Edip
Greenberg, Steven M.
van Rooden, Sanneke
author_facet Drenth, Nadieh
van der Grond, Jeroen
Rombouts, Serge A.R.B.
van Buchem, Mark A.
Terwindt, Gisela M.
Wermer, Marieke J.H.
Chhatwal, Jasmeer P.
Gurol, M. Edip
Greenberg, Steven M.
van Rooden, Sanneke
author_sort Drenth, Nadieh
collection PubMed
description Cerebral amyloid angiopathy (CAA) is a major cause of intracerebral hemorrhage and neurological decline in the elderly. CAA results in focal brain lesions, but the influence on global brain functioning needs further investigation. Here we study functional brain connectivity in patients with Dutch type hereditary CAA using resting state functional MRI. Twenty-four DNA-proven Dutch CAA mutation carriers (11 presymptomatic, 13 symptomatic) and 29 age-matched control subjects were included. Using a set of standardized networks covering the entire cortex, we assessed both within- and between-network functional connectivity. We investigated group differences using general linear models corrected for age, sex and gray matter volume. First, all mutation carriers were contrasted against control subjects and subsequently presymptomatic- and symptomatic mutation carriers against control subjects separately, to assess in which stage of the disease differences could be found. All mutation carriers grouped together showed decreased connectivity in the medial and lateral visual networks, default mode network, executive control and bilateral frontoparietal networks. Symptomatic carriers showed diminished connectivity in all but one network, and between the left and right frontoparietal networks. Presymptomatic carriers also showed diminished connectivity, but only in the frontoparietal left network. In conclusion, global brain functioning is diminished in patients with CAA, predominantly in symptomatic CAA and can therefore be considered to be a late consequence of the disease.
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spelling pubmed-78068792021-01-22 Cerebral amyloid angiopathy is associated with decreased functional brain connectivity Drenth, Nadieh van der Grond, Jeroen Rombouts, Serge A.R.B. van Buchem, Mark A. Terwindt, Gisela M. Wermer, Marieke J.H. Chhatwal, Jasmeer P. Gurol, M. Edip Greenberg, Steven M. van Rooden, Sanneke Neuroimage Clin Regular Article Cerebral amyloid angiopathy (CAA) is a major cause of intracerebral hemorrhage and neurological decline in the elderly. CAA results in focal brain lesions, but the influence on global brain functioning needs further investigation. Here we study functional brain connectivity in patients with Dutch type hereditary CAA using resting state functional MRI. Twenty-four DNA-proven Dutch CAA mutation carriers (11 presymptomatic, 13 symptomatic) and 29 age-matched control subjects were included. Using a set of standardized networks covering the entire cortex, we assessed both within- and between-network functional connectivity. We investigated group differences using general linear models corrected for age, sex and gray matter volume. First, all mutation carriers were contrasted against control subjects and subsequently presymptomatic- and symptomatic mutation carriers against control subjects separately, to assess in which stage of the disease differences could be found. All mutation carriers grouped together showed decreased connectivity in the medial and lateral visual networks, default mode network, executive control and bilateral frontoparietal networks. Symptomatic carriers showed diminished connectivity in all but one network, and between the left and right frontoparietal networks. Presymptomatic carriers also showed diminished connectivity, but only in the frontoparietal left network. In conclusion, global brain functioning is diminished in patients with CAA, predominantly in symptomatic CAA and can therefore be considered to be a late consequence of the disease. Elsevier 2020-12-24 /pmc/articles/PMC7806879/ /pubmed/33421870 http://dx.doi.org/10.1016/j.nicl.2020.102546 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Regular Article
Drenth, Nadieh
van der Grond, Jeroen
Rombouts, Serge A.R.B.
van Buchem, Mark A.
Terwindt, Gisela M.
Wermer, Marieke J.H.
Chhatwal, Jasmeer P.
Gurol, M. Edip
Greenberg, Steven M.
van Rooden, Sanneke
Cerebral amyloid angiopathy is associated with decreased functional brain connectivity
title Cerebral amyloid angiopathy is associated with decreased functional brain connectivity
title_full Cerebral amyloid angiopathy is associated with decreased functional brain connectivity
title_fullStr Cerebral amyloid angiopathy is associated with decreased functional brain connectivity
title_full_unstemmed Cerebral amyloid angiopathy is associated with decreased functional brain connectivity
title_short Cerebral amyloid angiopathy is associated with decreased functional brain connectivity
title_sort cerebral amyloid angiopathy is associated with decreased functional brain connectivity
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806879/
https://www.ncbi.nlm.nih.gov/pubmed/33421870
http://dx.doi.org/10.1016/j.nicl.2020.102546
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