Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Blanc, Clemence, Viguier, Alain, Calviere, Lionel, Planton, Mélanie, Albucher, Jean François, Rousseau, Vanessa, Sommet, Agnès, Bonneville, Fabrice, Pariente, Jérémie, Olivot, Jean Marc, Raposo, Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
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
_version_ 1783463746710011904
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
work_keys_str_mv AT blancclemence underlyingsmallvesseldiseaseassociatedwithmixedcerebralmicrobleeds
AT viguieralain underlyingsmallvesseldiseaseassociatedwithmixedcerebralmicrobleeds
AT calvierelionel underlyingsmallvesseldiseaseassociatedwithmixedcerebralmicrobleeds
AT plantonmelanie underlyingsmallvesseldiseaseassociatedwithmixedcerebralmicrobleeds
AT albucherjeanfrancois underlyingsmallvesseldiseaseassociatedwithmixedcerebralmicrobleeds
AT rousseauvanessa underlyingsmallvesseldiseaseassociatedwithmixedcerebralmicrobleeds
AT sommetagnes underlyingsmallvesseldiseaseassociatedwithmixedcerebralmicrobleeds
AT bonnevillefabrice underlyingsmallvesseldiseaseassociatedwithmixedcerebralmicrobleeds
AT parientejeremie underlyingsmallvesseldiseaseassociatedwithmixedcerebralmicrobleeds
AT olivotjeanmarc underlyingsmallvesseldiseaseassociatedwithmixedcerebralmicrobleeds
AT raposonicolas underlyingsmallvesseldiseaseassociatedwithmixedcerebralmicrobleeds