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Effects of Systolic Blood Pressure on Brain Integrity in Multiple Sclerosis

Background: In MS patients, hypertension is associated with a delayed diagnosis and an increased risk of progression. Understanding the mechanisms of this association could potentially lead to improved prevention of disease progression. We aimed to establish whether high blood pressure contributes t...

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Autores principales: Dossi, Daiana E., Chaves, Hernán, Heck, Evelyn S., Rodriguez Murúa, Sofía, Ventrice, Fernando, Bakshi, Rohit, Quintana, Francisco J., Correale, Jorge, Farez, Mauricio F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026666/
https://www.ncbi.nlm.nih.gov/pubmed/29988562
http://dx.doi.org/10.3389/fneur.2018.00487
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author Dossi, Daiana E.
Chaves, Hernán
Heck, Evelyn S.
Rodriguez Murúa, Sofía
Ventrice, Fernando
Bakshi, Rohit
Quintana, Francisco J.
Correale, Jorge
Farez, Mauricio F.
author_facet Dossi, Daiana E.
Chaves, Hernán
Heck, Evelyn S.
Rodriguez Murúa, Sofía
Ventrice, Fernando
Bakshi, Rohit
Quintana, Francisco J.
Correale, Jorge
Farez, Mauricio F.
author_sort Dossi, Daiana E.
collection PubMed
description Background: In MS patients, hypertension is associated with a delayed diagnosis and an increased risk of progression. Understanding the mechanisms of this association could potentially lead to improved prevention of disease progression. We aimed to establish whether high blood pressure contributes to white-matter injury and brain atrophy in MS. Methods: Cross-sectional study of 95 patients with RRMS. Estimates of fractional anisotropy, gray-matter volume and lesion load were obtained from 3T MRI. We used fractional anisotropy voxel-based statistics to establish the effect of blood pressure on white matter tracts. Additionally, we used voxel-based morphometry (VBM) to study the effect on gray matter integrity. Results: Only 29.5% had normal blood pressure levels, with 52.6% suffering from prehypertension and 17.9% with hypertension. Increasing systolic blood pressure was associated with damage to posterior white-matter tracts as well as greater levels of gray matter atrophy, in particular in the frontal cortex. Age-adjusted linear regression indicated that neither lesion volume (β = 0.002, 95%CI: 0.02–0.02; p = 0.85) or lesion number (β = −0.004, 95%CI: 0.03–0.02; p = 0.74) were associated with systolic blood pressure. Conclusions: Prehypertension and hypertension are frequent in MS. Increased blood pressure is related to white- and gray-matter integrity, both related to MS disability outcomes. These findings suggest attention to the control of blood pressure in MS patients.
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spelling pubmed-60266662018-07-09 Effects of Systolic Blood Pressure on Brain Integrity in Multiple Sclerosis Dossi, Daiana E. Chaves, Hernán Heck, Evelyn S. Rodriguez Murúa, Sofía Ventrice, Fernando Bakshi, Rohit Quintana, Francisco J. Correale, Jorge Farez, Mauricio F. Front Neurol Neurology Background: In MS patients, hypertension is associated with a delayed diagnosis and an increased risk of progression. Understanding the mechanisms of this association could potentially lead to improved prevention of disease progression. We aimed to establish whether high blood pressure contributes to white-matter injury and brain atrophy in MS. Methods: Cross-sectional study of 95 patients with RRMS. Estimates of fractional anisotropy, gray-matter volume and lesion load were obtained from 3T MRI. We used fractional anisotropy voxel-based statistics to establish the effect of blood pressure on white matter tracts. Additionally, we used voxel-based morphometry (VBM) to study the effect on gray matter integrity. Results: Only 29.5% had normal blood pressure levels, with 52.6% suffering from prehypertension and 17.9% with hypertension. Increasing systolic blood pressure was associated with damage to posterior white-matter tracts as well as greater levels of gray matter atrophy, in particular in the frontal cortex. Age-adjusted linear regression indicated that neither lesion volume (β = 0.002, 95%CI: 0.02–0.02; p = 0.85) or lesion number (β = −0.004, 95%CI: 0.03–0.02; p = 0.74) were associated with systolic blood pressure. Conclusions: Prehypertension and hypertension are frequent in MS. Increased blood pressure is related to white- and gray-matter integrity, both related to MS disability outcomes. These findings suggest attention to the control of blood pressure in MS patients. Frontiers Media S.A. 2018-06-25 /pmc/articles/PMC6026666/ /pubmed/29988562 http://dx.doi.org/10.3389/fneur.2018.00487 Text en Copyright © 2018 Dossi, Chaves, Heck, Rodriguez Murúa, Ventrice, Bakshi, Quintana, Correale and Farez. 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 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
Dossi, Daiana E.
Chaves, Hernán
Heck, Evelyn S.
Rodriguez Murúa, Sofía
Ventrice, Fernando
Bakshi, Rohit
Quintana, Francisco J.
Correale, Jorge
Farez, Mauricio F.
Effects of Systolic Blood Pressure on Brain Integrity in Multiple Sclerosis
title Effects of Systolic Blood Pressure on Brain Integrity in Multiple Sclerosis
title_full Effects of Systolic Blood Pressure on Brain Integrity in Multiple Sclerosis
title_fullStr Effects of Systolic Blood Pressure on Brain Integrity in Multiple Sclerosis
title_full_unstemmed Effects of Systolic Blood Pressure on Brain Integrity in Multiple Sclerosis
title_short Effects of Systolic Blood Pressure on Brain Integrity in Multiple Sclerosis
title_sort effects of systolic blood pressure on brain integrity in multiple sclerosis
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026666/
https://www.ncbi.nlm.nih.gov/pubmed/29988562
http://dx.doi.org/10.3389/fneur.2018.00487
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