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Correlation of blood pressure levels at different time periods throughout the day with total CSVD burden and MRI imaging markers

PURPOSE: Hypertension is an important risk factor for atherosclerotic cerebral small vessel disease (CSVD). Higher blood pressure is associated with a higher CSVD burden and the presence of relevant magnetic resonance imaging (MRI) markers. However, the effect of blood pressure level on CSVD burden...

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Autores principales: Yang, Hua, Fan, Xueyi, Shen, Xiangyi, Liang, Li, Hu, Dongyang, Zhang, Yimo, Liu, Li, Qian, Hairong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415676/
https://www.ncbi.nlm.nih.gov/pubmed/37576008
http://dx.doi.org/10.3389/fneur.2023.1200846
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author Yang, Hua
Fan, Xueyi
Shen, Xiangyi
Liang, Li
Hu, Dongyang
Zhang, Yimo
Liu, Li
Qian, Hairong
author_facet Yang, Hua
Fan, Xueyi
Shen, Xiangyi
Liang, Li
Hu, Dongyang
Zhang, Yimo
Liu, Li
Qian, Hairong
author_sort Yang, Hua
collection PubMed
description PURPOSE: Hypertension is an important risk factor for atherosclerotic cerebral small vessel disease (CSVD). Higher blood pressure is associated with a higher CSVD burden and the presence of relevant magnetic resonance imaging (MRI) markers. However, the effect of blood pressure level on CSVD burden and imaging markers including white matter hyperintensity (WHM), lacune, enlarged perivascular spaces (EPVS), and cerebral microbleed (CMB) remains unknown. The purpose of this study was to investigate the correlation between blood pressure level and CSVD burden at different time periods throughout the day. METHODS: In total, 144 in-patients with CSVD (66.4 ± 9.8 years, 50% male) were enrolled and underwent brain MRI, and 24-h ambulatory blood pressure was assessed. Patients were categorized into five groups according to their MRI-evaluated total CSVD burden scores (0–4). Spearman's correlation analysis was performed to examine the correlation between blood pressure levels at different time periods and the total CSVD score or the markers of periventricular WMH, deep WMH, lacune, EPVS, and CMB. RESULTS: Of the 144 patients, 83.3% (120/144) harbored one or more CSVD markers of interest. The systolic blood pressure (SBP) of 24-h, daytime, nighttime, and morning differed significantly among the five groups. The SBP levels increased significantly with the total CSVD scores during 24 h (P = 0.018), daytime (P = 0.018), and nighttime (P = 0.035). Spearman's correlation analysis demonstrated that the SBP of 24 h, daytime, nighttime, and morning and the diastolic blood pressure (DBP) of 24 h and morning positively and significantly correlated with the total CSVD score (P < 0.05). A logistic regression analysis indicated that both morning SBP and DBP were independent risk factors for total CSVD burden (OR = 1.13, 95% CI: 1.02–1.23, P = 0.015; OR = 1.19, 95% CI: 1.06–1.33, P = 0.005). Spearman's correlation analysis indicated a significant positive correlation between morning SBP and higher deep WMH Fazekas score (r = 0.296, P < 0.001), EPVS grade in the basal ganglia (r = 0.247, P = 0.003), and the presence of lacune (r = 0.173, P = 0.038) and CMB (r = 0.326, P < 0.001). Morning DBP only correlated positively with the presence of CMB (r = 0.292, P < 0.001). CONCLUSION: Higher SBP signficantly correlated with total CSVD burden in patients with atherosclerotic CSVD. Early morning blood pressure level is an important indicator to reflect the severity of CSVD patients.
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spelling pubmed-104156762023-08-12 Correlation of blood pressure levels at different time periods throughout the day with total CSVD burden and MRI imaging markers Yang, Hua Fan, Xueyi Shen, Xiangyi Liang, Li Hu, Dongyang Zhang, Yimo Liu, Li Qian, Hairong Front Neurol Neurology PURPOSE: Hypertension is an important risk factor for atherosclerotic cerebral small vessel disease (CSVD). Higher blood pressure is associated with a higher CSVD burden and the presence of relevant magnetic resonance imaging (MRI) markers. However, the effect of blood pressure level on CSVD burden and imaging markers including white matter hyperintensity (WHM), lacune, enlarged perivascular spaces (EPVS), and cerebral microbleed (CMB) remains unknown. The purpose of this study was to investigate the correlation between blood pressure level and CSVD burden at different time periods throughout the day. METHODS: In total, 144 in-patients with CSVD (66.4 ± 9.8 years, 50% male) were enrolled and underwent brain MRI, and 24-h ambulatory blood pressure was assessed. Patients were categorized into five groups according to their MRI-evaluated total CSVD burden scores (0–4). Spearman's correlation analysis was performed to examine the correlation between blood pressure levels at different time periods and the total CSVD score or the markers of periventricular WMH, deep WMH, lacune, EPVS, and CMB. RESULTS: Of the 144 patients, 83.3% (120/144) harbored one or more CSVD markers of interest. The systolic blood pressure (SBP) of 24-h, daytime, nighttime, and morning differed significantly among the five groups. The SBP levels increased significantly with the total CSVD scores during 24 h (P = 0.018), daytime (P = 0.018), and nighttime (P = 0.035). Spearman's correlation analysis demonstrated that the SBP of 24 h, daytime, nighttime, and morning and the diastolic blood pressure (DBP) of 24 h and morning positively and significantly correlated with the total CSVD score (P < 0.05). A logistic regression analysis indicated that both morning SBP and DBP were independent risk factors for total CSVD burden (OR = 1.13, 95% CI: 1.02–1.23, P = 0.015; OR = 1.19, 95% CI: 1.06–1.33, P = 0.005). Spearman's correlation analysis indicated a significant positive correlation between morning SBP and higher deep WMH Fazekas score (r = 0.296, P < 0.001), EPVS grade in the basal ganglia (r = 0.247, P = 0.003), and the presence of lacune (r = 0.173, P = 0.038) and CMB (r = 0.326, P < 0.001). Morning DBP only correlated positively with the presence of CMB (r = 0.292, P < 0.001). CONCLUSION: Higher SBP signficantly correlated with total CSVD burden in patients with atherosclerotic CSVD. Early morning blood pressure level is an important indicator to reflect the severity of CSVD patients. Frontiers Media S.A. 2023-07-25 /pmc/articles/PMC10415676/ /pubmed/37576008 http://dx.doi.org/10.3389/fneur.2023.1200846 Text en Copyright © 2023 Yang, Fan, Shen, Liang, Hu, Zhang, Liu and Qian. https://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
Yang, Hua
Fan, Xueyi
Shen, Xiangyi
Liang, Li
Hu, Dongyang
Zhang, Yimo
Liu, Li
Qian, Hairong
Correlation of blood pressure levels at different time periods throughout the day with total CSVD burden and MRI imaging markers
title Correlation of blood pressure levels at different time periods throughout the day with total CSVD burden and MRI imaging markers
title_full Correlation of blood pressure levels at different time periods throughout the day with total CSVD burden and MRI imaging markers
title_fullStr Correlation of blood pressure levels at different time periods throughout the day with total CSVD burden and MRI imaging markers
title_full_unstemmed Correlation of blood pressure levels at different time periods throughout the day with total CSVD burden and MRI imaging markers
title_short Correlation of blood pressure levels at different time periods throughout the day with total CSVD burden and MRI imaging markers
title_sort correlation of blood pressure levels at different time periods throughout the day with total csvd burden and mri imaging markers
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415676/
https://www.ncbi.nlm.nih.gov/pubmed/37576008
http://dx.doi.org/10.3389/fneur.2023.1200846
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