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Arterial Stiffness in Patients with Deep and Lobar Intracerebral Hemorrhage

BACKGROUND AND PURPOSE: Intracerebral hemorrhage (ICH) accounts for approximately 10% of stroke cases. Hypertension may play a role in the pathogenesis of ICH that occurs in the basal ganglia, thalamus, pons, and cerebellum, but not in that of lobar ICH. Hypertension contributes to decreased elastic...

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Autores principales: Acampa, Maurizio, Guideri, Francesca, Di Donato, Ilaria, Tassi, Rossana, Marotta, Giovanna, Lo Giudice, Giuseppe, D'Andrea, Paolo, Martini, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Stroke Society 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4200589/
https://www.ncbi.nlm.nih.gov/pubmed/25328877
http://dx.doi.org/10.5853/jos.2014.16.3.184
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author Acampa, Maurizio
Guideri, Francesca
Di Donato, Ilaria
Tassi, Rossana
Marotta, Giovanna
Lo Giudice, Giuseppe
D'Andrea, Paolo
Martini, Giuseppe
author_facet Acampa, Maurizio
Guideri, Francesca
Di Donato, Ilaria
Tassi, Rossana
Marotta, Giovanna
Lo Giudice, Giuseppe
D'Andrea, Paolo
Martini, Giuseppe
author_sort Acampa, Maurizio
collection PubMed
description BACKGROUND AND PURPOSE: Intracerebral hemorrhage (ICH) accounts for approximately 10% of stroke cases. Hypertension may play a role in the pathogenesis of ICH that occurs in the basal ganglia, thalamus, pons, and cerebellum, but not in that of lobar ICH. Hypertension contributes to decreased elasticity of arteries, thereby increasing the likelihood of rupture in response to acute elevation in intravascular pressure. This study aimed to evaluate arterial stiffness (using the arterial stiffness index [ASI]) in patients with deep (putaminal and thalamic) ICH in comparison with patients with lobar ICH. METHODS: We enrolled 64 patients (mean±SD age: 69.3±10.7 years; 47 men and 17 women) among 73 who referred consecutively to our department for intraparenchymal hemorrhage and underwent brain computed tomography (CT) and cerebral angio-CT. In all the subjects, 24-hour heart rates and blood pressures were monitored. The linear regression slope of diastolic on systolic blood pressure was assumed as a global measure of arterial compliance, and its complement (1 minus the slope), ASI, has been considered as a measure of arterial stiffness. RESULTS: In the patients with deep ICH, ASI was significantly higher than in the patients with lobar ICH (0.64±0.19 vs. 0.53±0.17, P=0.04). CONCLUSIONS: Our results suggest that in deep ICH, arterial stiffening represents a possible pathogenetic factor that modifies arterial wall properties and contributes to vascular rupture in response to intravascular pressure acute elevation. Therapeutic strategies that reduce arterial stiffness may potentially lower the incidence of deep hemorrhagic stroke.
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spelling pubmed-42005892014-10-17 Arterial Stiffness in Patients with Deep and Lobar Intracerebral Hemorrhage Acampa, Maurizio Guideri, Francesca Di Donato, Ilaria Tassi, Rossana Marotta, Giovanna Lo Giudice, Giuseppe D'Andrea, Paolo Martini, Giuseppe J Stroke Original Article BACKGROUND AND PURPOSE: Intracerebral hemorrhage (ICH) accounts for approximately 10% of stroke cases. Hypertension may play a role in the pathogenesis of ICH that occurs in the basal ganglia, thalamus, pons, and cerebellum, but not in that of lobar ICH. Hypertension contributes to decreased elasticity of arteries, thereby increasing the likelihood of rupture in response to acute elevation in intravascular pressure. This study aimed to evaluate arterial stiffness (using the arterial stiffness index [ASI]) in patients with deep (putaminal and thalamic) ICH in comparison with patients with lobar ICH. METHODS: We enrolled 64 patients (mean±SD age: 69.3±10.7 years; 47 men and 17 women) among 73 who referred consecutively to our department for intraparenchymal hemorrhage and underwent brain computed tomography (CT) and cerebral angio-CT. In all the subjects, 24-hour heart rates and blood pressures were monitored. The linear regression slope of diastolic on systolic blood pressure was assumed as a global measure of arterial compliance, and its complement (1 minus the slope), ASI, has been considered as a measure of arterial stiffness. RESULTS: In the patients with deep ICH, ASI was significantly higher than in the patients with lobar ICH (0.64±0.19 vs. 0.53±0.17, P=0.04). CONCLUSIONS: Our results suggest that in deep ICH, arterial stiffening represents a possible pathogenetic factor that modifies arterial wall properties and contributes to vascular rupture in response to intravascular pressure acute elevation. Therapeutic strategies that reduce arterial stiffness may potentially lower the incidence of deep hemorrhagic stroke. Korean Stroke Society 2014-09 2014-09-30 /pmc/articles/PMC4200589/ /pubmed/25328877 http://dx.doi.org/10.5853/jos.2014.16.3.184 Text en Copyright © 2014 Korean Stroke Society http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Acampa, Maurizio
Guideri, Francesca
Di Donato, Ilaria
Tassi, Rossana
Marotta, Giovanna
Lo Giudice, Giuseppe
D'Andrea, Paolo
Martini, Giuseppe
Arterial Stiffness in Patients with Deep and Lobar Intracerebral Hemorrhage
title Arterial Stiffness in Patients with Deep and Lobar Intracerebral Hemorrhage
title_full Arterial Stiffness in Patients with Deep and Lobar Intracerebral Hemorrhage
title_fullStr Arterial Stiffness in Patients with Deep and Lobar Intracerebral Hemorrhage
title_full_unstemmed Arterial Stiffness in Patients with Deep and Lobar Intracerebral Hemorrhage
title_short Arterial Stiffness in Patients with Deep and Lobar Intracerebral Hemorrhage
title_sort arterial stiffness in patients with deep and lobar intracerebral hemorrhage
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4200589/
https://www.ncbi.nlm.nih.gov/pubmed/25328877
http://dx.doi.org/10.5853/jos.2014.16.3.184
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