Theresa J van Lith, Esther Janssen, Jan-Willem van Dalen, Hao Li, Mats Koeneman, Wouter M Sluis, Naomi T Wijers, Marieke J H Wermer, Menno V Huisman, H Bart van der Worp, Frederick J A Meijer, Anil M Tuladhar, Sebastian J H Bredie, Frank-Erik de Leeuw
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We examined whether BPV, measured in-hospital using continuous monitoring, is associated with WM microstructural integrity in COVID-19 patients.</p><p><strong>Methods: </strong>We included hospitalised COVID-19 patients from the CORONavirus and Ischemic Stroke (CORONIS) study who underwent continuous vital signs monitoring using a wearable device during hospital admission and had an MRI shortly after discharge. Systolic BPV was calculated as Average Real Variability (ARV) and Coefficient of Variation (CV) with 1-, 5- and 20-minute intervals. We used diffusion tensor imaging to assess fractional anisotropy (FA) and peak width of skeletonised mean diffusivity (PSMD) as markers of WM integrity. Associations between BPV and WM integrity were examined with linear regression adjusted for age, mean systolic blood pressure (BP), number of BP measurements and type of respiratory support.</p><p><strong>Results: </strong>We included 47 COVID-19 patients (mean age: 59.6 years). 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引用次数: 0
摘要
背景:高血压变异性(BPV)与脑血管损伤和痴呆相关,但尚不清楚住院期间的短期BPV是否也与脑白质(WM)损伤相关。我们研究了在医院使用连续监测测量的BPV是否与COVID-19患者WM微结构完整性相关。方法:我们纳入了冠状病毒与缺血性卒中(CORONIS)研究中住院的COVID-19患者,这些患者在入院期间使用可穿戴设备连续监测生命体征,出院后不久进行MRI检查。收缩期BPV以平均真实变异性(ARV)和变异系数(CV)计算,时间间隔分别为1、5和20分钟。我们使用扩散张量成像来评估分数各向异性(FA)和骨架平均扩散率(PSMD)的峰宽作为WM完整性的标记。采用线性回归对年龄、平均收缩压(BP)、血压测量次数和呼吸支持类型进行校正,检验BPV和WM完整性之间的关系。结果:纳入47例COVID-19患者,平均年龄59.6岁。每位患者测量血压6306±4343次(中位入院时间:11天(四分位间距[IQR] 7.5-15.0)。较高的ARV和CV均与较低的WM显微结构完整性相关,反映为较低的FA (ARV: β = -0.40, p = 0.010;校正混杂因素后,CV: β = -0.33, p = 0.026)和更高的PSMD (CV: β = 0.28, p = 0.038)。对WM高强度的校正并没有改变这些结果。结论:住院期间高BPV与COVID-19患者较低的WM完整性相关,尽管因果关系有待证实。我们的发现需要在没有COVID-19的住院患者中进行验证,以检验其普遍性。
Higher blood pressure variability during hospitalisation is associated with lower cerebral white matter integrity in COVID-19 patients.
Background: High blood pressure variability (BPV) is associated with cerebrovascular damage and dementia, but it is unknown whether short-term BPV during hospitalisation is also associated with cerebral white matter (WM) damage. We examined whether BPV, measured in-hospital using continuous monitoring, is associated with WM microstructural integrity in COVID-19 patients.
Methods: We included hospitalised COVID-19 patients from the CORONavirus and Ischemic Stroke (CORONIS) study who underwent continuous vital signs monitoring using a wearable device during hospital admission and had an MRI shortly after discharge. Systolic BPV was calculated as Average Real Variability (ARV) and Coefficient of Variation (CV) with 1-, 5- and 20-minute intervals. We used diffusion tensor imaging to assess fractional anisotropy (FA) and peak width of skeletonised mean diffusivity (PSMD) as markers of WM integrity. Associations between BPV and WM integrity were examined with linear regression adjusted for age, mean systolic blood pressure (BP), number of BP measurements and type of respiratory support.
Results: We included 47 COVID-19 patients (mean age: 59.6 years). BP was measured 6306 ± 4343 times per patient (median admission: 11 days (Interquartile Range [IQR] 7.5-15.0). Both higher ARV and CV were associated with lower WM microstructural integrity, reflected by lower FA (ARV: β = -0.40, p = .010; CV: β = -0.33, p = 0.026) and higher PSMD (CV: β = 0.28, p = .038) after adjustment for confounders. Correction for WM hyperintensities did not change these results.
Conclusions: High BPV during hospitalisation is associated with lower WM integrity in COVID-19 patients, although causality needs to be demonstrated. Our findings need validation in hospitalised patients without COVID-19 to examine generalisability.
Blood PressureMedicine-Cardiology and Cardiovascular Medicine
CiteScore
3.20
自引率
5.60%
发文量
41
期刊介绍:
For outstanding coverage of the latest advances in hypertension research, turn to Blood Pressure, a primary source for authoritative and timely information on all aspects of hypertension research and management.
Features include:
• Physiology and pathophysiology of blood pressure regulation
• Primary and secondary hypertension
• Cerebrovascular and cardiovascular complications of hypertension
• Detection, treatment and follow-up of hypertension
• Non pharmacological and pharmacological management
• Large outcome trials in hypertension.