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Total Burden of Cerebral Small Vessel Disease in Recurrent ICH versus First-ever ICH
The relationship between recurrent intracerebral hemorrhage (ICH) and total burden of cerebral small vessel disease (CSVD) is not completely investigated. We aimed to study whether recurrent intracerebral hemorrhage (ICH) had higher CSVD score than first-ever ICH. Lacunes, white matter hyperintensit...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
JKL International LLC
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6538213/ https://www.ncbi.nlm.nih.gov/pubmed/31165001 http://dx.doi.org/10.14336/AD.2018.0804 |
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author | Xu, Mangmang Cheng, Yajun Song, Quhong Yuan, Ruozhen Zhang, Shuting Hao, Zilong Liu, Ming |
author_facet | Xu, Mangmang Cheng, Yajun Song, Quhong Yuan, Ruozhen Zhang, Shuting Hao, Zilong Liu, Ming |
author_sort | Xu, Mangmang |
collection | PubMed |
description | The relationship between recurrent intracerebral hemorrhage (ICH) and total burden of cerebral small vessel disease (CSVD) is not completely investigated. We aimed to study whether recurrent intracerebral hemorrhage (ICH) had higher CSVD score than first-ever ICH. Lacunes, white matter hyperintensities (WMH), cerebral microbleeds (CMBs), enlarged perivascular spaces (EPVS), cortical superficial siderosis (cSS) and CSVD score were rated on brain magnetic resonance imaging (MRI) in primary ICH patients. Recurrent ICHs were confirmed by reviewing the medical records and MRI scans. Mixed hematomas were defined as follows: deep + lobar, deep + cerebellar, or deep + lobar + cerebellar. Of the 184 patients with primary ICH enrolled (mean age, 61.0 years; 75.5% men), recurrent ICH was present in 45 (24.5%) patients; 26.1% (48/184) had ≥2 hematomas, 93.8% (45/48) of which exhibited recurrent ICH. Mixed hematomas were identified in 8.7% (16/184) of patients and bilateral hematomas in 17.9% (33/184). All mixed hematomas and bilateral hematomas were from cases of recurrent ICH. Patients with mixed etiology-ICH were more likely to have recurrent ICH than patients with cerebral amyloid angiopathy (CAA) or hypertensive angiopathy (HA)-related ICH (36.8% vs17.8%, p=0.008). Multivariate ordinal regression analysis showed that the presence of recurrent ICH (p=0.001), ≥2 hematomas (p=0.002), mixed hematomas (p<0.00001), and bilateral hematomas (p=0.002) were separately significantly associated with a high CSVD score. Recurrent ICH occurs mostly among patients with mixed etiology-ICH and is associated with a higher CSVD burden than first-ever ICH, which needs to be verified by future larger studies. |
format | Online Article Text |
id | pubmed-6538213 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | JKL International LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-65382132019-06-05 Total Burden of Cerebral Small Vessel Disease in Recurrent ICH versus First-ever ICH Xu, Mangmang Cheng, Yajun Song, Quhong Yuan, Ruozhen Zhang, Shuting Hao, Zilong Liu, Ming Aging Dis Orginal Article The relationship between recurrent intracerebral hemorrhage (ICH) and total burden of cerebral small vessel disease (CSVD) is not completely investigated. We aimed to study whether recurrent intracerebral hemorrhage (ICH) had higher CSVD score than first-ever ICH. Lacunes, white matter hyperintensities (WMH), cerebral microbleeds (CMBs), enlarged perivascular spaces (EPVS), cortical superficial siderosis (cSS) and CSVD score were rated on brain magnetic resonance imaging (MRI) in primary ICH patients. Recurrent ICHs were confirmed by reviewing the medical records and MRI scans. Mixed hematomas were defined as follows: deep + lobar, deep + cerebellar, or deep + lobar + cerebellar. Of the 184 patients with primary ICH enrolled (mean age, 61.0 years; 75.5% men), recurrent ICH was present in 45 (24.5%) patients; 26.1% (48/184) had ≥2 hematomas, 93.8% (45/48) of which exhibited recurrent ICH. Mixed hematomas were identified in 8.7% (16/184) of patients and bilateral hematomas in 17.9% (33/184). All mixed hematomas and bilateral hematomas were from cases of recurrent ICH. Patients with mixed etiology-ICH were more likely to have recurrent ICH than patients with cerebral amyloid angiopathy (CAA) or hypertensive angiopathy (HA)-related ICH (36.8% vs17.8%, p=0.008). Multivariate ordinal regression analysis showed that the presence of recurrent ICH (p=0.001), ≥2 hematomas (p=0.002), mixed hematomas (p<0.00001), and bilateral hematomas (p=0.002) were separately significantly associated with a high CSVD score. Recurrent ICH occurs mostly among patients with mixed etiology-ICH and is associated with a higher CSVD burden than first-ever ICH, which needs to be verified by future larger studies. JKL International LLC 2019-06-01 /pmc/articles/PMC6538213/ /pubmed/31165001 http://dx.doi.org/10.14336/AD.2018.0804 Text en Copyright: © 2019 Xu et al. http://creativecommons.org/licenses/by/2.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Orginal Article Xu, Mangmang Cheng, Yajun Song, Quhong Yuan, Ruozhen Zhang, Shuting Hao, Zilong Liu, Ming Total Burden of Cerebral Small Vessel Disease in Recurrent ICH versus First-ever ICH |
title | Total Burden of Cerebral Small Vessel Disease in Recurrent ICH versus First-ever ICH |
title_full | Total Burden of Cerebral Small Vessel Disease in Recurrent ICH versus First-ever ICH |
title_fullStr | Total Burden of Cerebral Small Vessel Disease in Recurrent ICH versus First-ever ICH |
title_full_unstemmed | Total Burden of Cerebral Small Vessel Disease in Recurrent ICH versus First-ever ICH |
title_short | Total Burden of Cerebral Small Vessel Disease in Recurrent ICH versus First-ever ICH |
title_sort | total burden of cerebral small vessel disease in recurrent ich versus first-ever ich |
topic | Orginal Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6538213/ https://www.ncbi.nlm.nih.gov/pubmed/31165001 http://dx.doi.org/10.14336/AD.2018.0804 |
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