Cargando…

Spatial distribution of cerebral microbleeds reveals heterogeneous pathogenesis in CADASIL

OBJECTIVES: Radiological diagnosis of subtypes of cerebral small vessel diseases remains challenging. This study aimed to explore the spatial distribution of cerebral microbleeds (CMBs) in cerebral autosomal dominant arteriopathy with subcortical infarct and leukoencephalopathy (CADASIL) in contrast...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Ya-Fang, Chen, Chih-Hao, Wu, Wen-Chau, Lee, Bo-Ching, Tsai, Hsin-Hsi, Tang, Sung-Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831253/
https://www.ncbi.nlm.nih.gov/pubmed/34698928
http://dx.doi.org/10.1007/s00330-021-08288-9
_version_ 1784648465324703744
author Chen, Ya-Fang
Chen, Chih-Hao
Wu, Wen-Chau
Lee, Bo-Ching
Tsai, Hsin-Hsi
Tang, Sung-Chun
author_facet Chen, Ya-Fang
Chen, Chih-Hao
Wu, Wen-Chau
Lee, Bo-Ching
Tsai, Hsin-Hsi
Tang, Sung-Chun
author_sort Chen, Ya-Fang
collection PubMed
description OBJECTIVES: Radiological diagnosis of subtypes of cerebral small vessel diseases remains challenging. This study aimed to explore the spatial distribution of cerebral microbleeds (CMBs) in cerebral autosomal dominant arteriopathy with subcortical infarct and leukoencephalopathy (CADASIL) in contrast to cerebral amyloid angiopathy (CAA) in the lobar regions. METHODS: Thirty-two patients with CADASIL and 33 patients with probable CAA were prospectively and consecutively included. On 3-Tesla susceptibility-weighted magnetic resonance images, CMBs were analyzed for incidence and volume within atlas-based regions of interest, followed by voxel-wise analysis using risk mapping. The distribution of CMBs was correlated with the status of hypertension. Correlation and group differences with a p-value less than 0.05 were considered to be significant. RESULTS: As compared with the CAA group, the CADASIL group presents a larger CMB volume in hippocampus/amygdala and white matter (nonparametric analysis of covariance, p = 0.014 and 0.037, respectively), a smaller CMB volume in parietal lobe (p = 0.038), and a higher incidence in hippocampus/amygdala, white matter, and insula (logistic regression, p = 0.019, 0.024, and 0.30, respectively). As part of the exclusion criteria of probable CAA, thalamus, basal ganglia, and pons exhibit greater CMB volume/incidence in the CADASIL group. In CADASIL patients, hot spots of CMBs are identified in the putamen and posteromedial thalamus; hypertension is associated with larger CMB volumes in insula, basal ganglia, and pons. CONCLUSIONS: The spatial distribution of CMBs is differentiable between CADASIL and CAA in lobar regions. In CADASIL patients, hypertension has a region-dependent mediating effect on the CMB volume. KEY POINTS: • The topological distribution of lobar CMBs is differentiable between CADASIL and CAA. • In CADASIL patients, hypertension mediates CMB volume and the mediation is region dependent. • CMB risk mapping allows for voxel-wise exploration of CMB distribution and reveals hot spots in the putamen and posteromedial thalamus in CADASIL.
format Online
Article
Text
id pubmed-8831253
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-88312532022-02-23 Spatial distribution of cerebral microbleeds reveals heterogeneous pathogenesis in CADASIL Chen, Ya-Fang Chen, Chih-Hao Wu, Wen-Chau Lee, Bo-Ching Tsai, Hsin-Hsi Tang, Sung-Chun Eur Radiol Neuro OBJECTIVES: Radiological diagnosis of subtypes of cerebral small vessel diseases remains challenging. This study aimed to explore the spatial distribution of cerebral microbleeds (CMBs) in cerebral autosomal dominant arteriopathy with subcortical infarct and leukoencephalopathy (CADASIL) in contrast to cerebral amyloid angiopathy (CAA) in the lobar regions. METHODS: Thirty-two patients with CADASIL and 33 patients with probable CAA were prospectively and consecutively included. On 3-Tesla susceptibility-weighted magnetic resonance images, CMBs were analyzed for incidence and volume within atlas-based regions of interest, followed by voxel-wise analysis using risk mapping. The distribution of CMBs was correlated with the status of hypertension. Correlation and group differences with a p-value less than 0.05 were considered to be significant. RESULTS: As compared with the CAA group, the CADASIL group presents a larger CMB volume in hippocampus/amygdala and white matter (nonparametric analysis of covariance, p = 0.014 and 0.037, respectively), a smaller CMB volume in parietal lobe (p = 0.038), and a higher incidence in hippocampus/amygdala, white matter, and insula (logistic regression, p = 0.019, 0.024, and 0.30, respectively). As part of the exclusion criteria of probable CAA, thalamus, basal ganglia, and pons exhibit greater CMB volume/incidence in the CADASIL group. In CADASIL patients, hot spots of CMBs are identified in the putamen and posteromedial thalamus; hypertension is associated with larger CMB volumes in insula, basal ganglia, and pons. CONCLUSIONS: The spatial distribution of CMBs is differentiable between CADASIL and CAA in lobar regions. In CADASIL patients, hypertension has a region-dependent mediating effect on the CMB volume. KEY POINTS: • The topological distribution of lobar CMBs is differentiable between CADASIL and CAA. • In CADASIL patients, hypertension mediates CMB volume and the mediation is region dependent. • CMB risk mapping allows for voxel-wise exploration of CMB distribution and reveals hot spots in the putamen and posteromedial thalamus in CADASIL. Springer Berlin Heidelberg 2021-10-26 2022 /pmc/articles/PMC8831253/ /pubmed/34698928 http://dx.doi.org/10.1007/s00330-021-08288-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Neuro
Chen, Ya-Fang
Chen, Chih-Hao
Wu, Wen-Chau
Lee, Bo-Ching
Tsai, Hsin-Hsi
Tang, Sung-Chun
Spatial distribution of cerebral microbleeds reveals heterogeneous pathogenesis in CADASIL
title Spatial distribution of cerebral microbleeds reveals heterogeneous pathogenesis in CADASIL
title_full Spatial distribution of cerebral microbleeds reveals heterogeneous pathogenesis in CADASIL
title_fullStr Spatial distribution of cerebral microbleeds reveals heterogeneous pathogenesis in CADASIL
title_full_unstemmed Spatial distribution of cerebral microbleeds reveals heterogeneous pathogenesis in CADASIL
title_short Spatial distribution of cerebral microbleeds reveals heterogeneous pathogenesis in CADASIL
title_sort spatial distribution of cerebral microbleeds reveals heterogeneous pathogenesis in cadasil
topic Neuro
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831253/
https://www.ncbi.nlm.nih.gov/pubmed/34698928
http://dx.doi.org/10.1007/s00330-021-08288-9
work_keys_str_mv AT chenyafang spatialdistributionofcerebralmicrobleedsrevealsheterogeneouspathogenesisincadasil
AT chenchihhao spatialdistributionofcerebralmicrobleedsrevealsheterogeneouspathogenesisincadasil
AT wuwenchau spatialdistributionofcerebralmicrobleedsrevealsheterogeneouspathogenesisincadasil
AT leeboching spatialdistributionofcerebralmicrobleedsrevealsheterogeneouspathogenesisincadasil
AT tsaihsinhsi spatialdistributionofcerebralmicrobleedsrevealsheterogeneouspathogenesisincadasil
AT tangsungchun spatialdistributionofcerebralmicrobleedsrevealsheterogeneouspathogenesisincadasil