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Underlying Small Vessel Disease Associated With Mixed Cerebral Microbleeds
Background and Purpose: Whether patients with both lobar and deep cerebral microbleeds (mixed CMB) have advanced cerebral amyloid angiopathy (CAA), hypertensive angiopathy (HA) or both is uncertain. To get insight into the underlying small vessel disease (SVD) associated with mixed CMB, we explored...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819505/ https://www.ncbi.nlm.nih.gov/pubmed/31708859 http://dx.doi.org/10.3389/fneur.2019.01126 |
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author | Blanc, Clemence Viguier, Alain Calviere, Lionel Planton, Mélanie Albucher, Jean François Rousseau, Vanessa Sommet, Agnès Bonneville, Fabrice Pariente, Jérémie Olivot, Jean Marc Raposo, Nicolas |
author_facet | Blanc, Clemence Viguier, Alain Calviere, Lionel Planton, Mélanie Albucher, Jean François Rousseau, Vanessa Sommet, Agnès Bonneville, Fabrice Pariente, Jérémie Olivot, Jean Marc Raposo, Nicolas |
author_sort | Blanc, Clemence |
collection | PubMed |
description | Background and Purpose: Whether patients with both lobar and deep cerebral microbleeds (mixed CMB) have advanced cerebral amyloid angiopathy (CAA), hypertensive angiopathy (HA) or both is uncertain. To get insight into the underlying small vessel disease (SVD) associated with mixed CMB, we explored its association with cortical superficial siderosis (cSS), a key marker of CAA and other MRI markers of SVD in patients with intracerebral hemorrhage (ICH). Methods: Of 425 consecutive patients with acute ICH who had received brain MRIs, 260 had ≥1 CMB and were included in the analysis. They were categorized as strictly lobar CMB (suggesting CAA), strictly deep CMB (suggesting HA) or mixed CMB. Clinical and imaging characteristics were compared (1) between the three CMB groups and (2) within mixed CMB patients according to the symptomatic ICH location. Results: Overall, 111 (26%) patients had mixed CMB. Compared to strictly lobar CMB (n = 111) and strictly deep CMB (n = 38), patients with mixed CMB had a more severe burden of lacune, white matter hyperintensities and CMB. cSS was observed in 24.3% of patients with mixed CMB compared to 44.1% in strictly lobar CMB and 10.5% in strictly deep CMB (p < 0.0001). Among patients with mixed CMB, 44 (39.6%) had a lobar symptomatic ICH and 67 (60.4%) had a non-lobar ICH. Patients with non-lobar ICH were more likely to have hypertension, whereas those with lobar ICH were more likely to have cSS and chronic lobar ICH and had higher ratio lobar CMB count/total CMB count. Conclusions: Mixed CMB is frequently encountered in patients with ICH and appears as a heterogeneous group, suggesting that both CAA and HA may be contributing to mixed CMB. Neuroimaging markers including ICH location, cSS, and CMB distribution may indicate the predominant underlying vasculopathy, with potential prognostic implications. |
format | Online Article Text |
id | pubmed-6819505 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68195052019-11-08 Underlying Small Vessel Disease Associated With Mixed Cerebral Microbleeds Blanc, Clemence Viguier, Alain Calviere, Lionel Planton, Mélanie Albucher, Jean François Rousseau, Vanessa Sommet, Agnès Bonneville, Fabrice Pariente, Jérémie Olivot, Jean Marc Raposo, Nicolas Front Neurol Neurology Background and Purpose: Whether patients with both lobar and deep cerebral microbleeds (mixed CMB) have advanced cerebral amyloid angiopathy (CAA), hypertensive angiopathy (HA) or both is uncertain. To get insight into the underlying small vessel disease (SVD) associated with mixed CMB, we explored its association with cortical superficial siderosis (cSS), a key marker of CAA and other MRI markers of SVD in patients with intracerebral hemorrhage (ICH). Methods: Of 425 consecutive patients with acute ICH who had received brain MRIs, 260 had ≥1 CMB and were included in the analysis. They were categorized as strictly lobar CMB (suggesting CAA), strictly deep CMB (suggesting HA) or mixed CMB. Clinical and imaging characteristics were compared (1) between the three CMB groups and (2) within mixed CMB patients according to the symptomatic ICH location. Results: Overall, 111 (26%) patients had mixed CMB. Compared to strictly lobar CMB (n = 111) and strictly deep CMB (n = 38), patients with mixed CMB had a more severe burden of lacune, white matter hyperintensities and CMB. cSS was observed in 24.3% of patients with mixed CMB compared to 44.1% in strictly lobar CMB and 10.5% in strictly deep CMB (p < 0.0001). Among patients with mixed CMB, 44 (39.6%) had a lobar symptomatic ICH and 67 (60.4%) had a non-lobar ICH. Patients with non-lobar ICH were more likely to have hypertension, whereas those with lobar ICH were more likely to have cSS and chronic lobar ICH and had higher ratio lobar CMB count/total CMB count. Conclusions: Mixed CMB is frequently encountered in patients with ICH and appears as a heterogeneous group, suggesting that both CAA and HA may be contributing to mixed CMB. Neuroimaging markers including ICH location, cSS, and CMB distribution may indicate the predominant underlying vasculopathy, with potential prognostic implications. Frontiers Media S.A. 2019-10-23 /pmc/articles/PMC6819505/ /pubmed/31708859 http://dx.doi.org/10.3389/fneur.2019.01126 Text en Copyright © 2019 Blanc, Viguier, Calviere, Planton, Albucher, Rousseau, Sommet, Bonneville, Pariente, Olivot and Raposo. http://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 | Neurology Blanc, Clemence Viguier, Alain Calviere, Lionel Planton, Mélanie Albucher, Jean François Rousseau, Vanessa Sommet, Agnès Bonneville, Fabrice Pariente, Jérémie Olivot, Jean Marc Raposo, Nicolas Underlying Small Vessel Disease Associated With Mixed Cerebral Microbleeds |
title | Underlying Small Vessel Disease Associated With Mixed Cerebral Microbleeds |
title_full | Underlying Small Vessel Disease Associated With Mixed Cerebral Microbleeds |
title_fullStr | Underlying Small Vessel Disease Associated With Mixed Cerebral Microbleeds |
title_full_unstemmed | Underlying Small Vessel Disease Associated With Mixed Cerebral Microbleeds |
title_short | Underlying Small Vessel Disease Associated With Mixed Cerebral Microbleeds |
title_sort | underlying small vessel disease associated with mixed cerebral microbleeds |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819505/ https://www.ncbi.nlm.nih.gov/pubmed/31708859 http://dx.doi.org/10.3389/fneur.2019.01126 |
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