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缺血性中风后的血压变异性与脑白质高信号

Blood pressure variability and white matter hyperintensities after ischemic stroke.

作者信息

Hilkens Nina A, de Leeuw Frank-Erik, Klijn Catharina Jm, Richard Edo

机构信息

Department of Neurology, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, the Netherlands.

出版信息

Cereb Circ Cogn Behav. 2024 Jan 12;6:100205. doi: 10.1016/j.cccb.2024.100205. eCollection 2024.

Abstract

BACKGROUND

High blood pressure variability (BPV) may be a risk factor for stroke and dementia in patients with ischemic stroke, but the underlying mechanism is unknown. We aimed to investigate whether high BPV is associated with presence and progression of white matter hyperintensities (WMH).

METHODS

We performed a post-hoc analysis on the MRI substudy of the PRoFESS trial, including 771 patients with ischemic stroke who underwent MRI at baseline and after a median of 2.1 years. WMH were rated with a semi-quantitative scale. Visit-to-visit BPV was expressed as the coefficient of variation (interval 3-6 months, median number of visits 7). The association of BPV with WMH burden and progression was assessed with linear and logistic regression analyses adjusted for confounders.

RESULTS

BPV was associated with burden of periventricular WMH (β 0.36 95%CI 0.19-0.53, per one SD increase in BPV) and subcortical (log-transformed) WMH (β 0.25, 95%CI 0.08-0.42). BPV was not associated with periventricular (OR 1.09, 95%CI 0.94-1.27) and subcortical WMH progression (OR 1.15, 95%CI 0.99-1.35). Associations were independent of mean BP.

CONCLUSION

High visit-to-visit BPV was associated with both subcortical and periventricular WMH burden in patients with ischemic stroke, but not with WMH progression in this study.

摘要

背景

高血压变异性(BPV)可能是缺血性脑卒中患者发生卒中和痴呆的危险因素,但其潜在机制尚不清楚。我们旨在研究高BPV是否与白质高信号(WMH)的存在和进展相关。

方法

我们对PRoFESS试验的MRI子研究进行了事后分析,纳入771例缺血性脑卒中患者,这些患者在基线时和中位2.1年后接受了MRI检查。WMH采用半定量量表进行评分。就诊间BPV表示为变异系数(间隔3 - 6个月,就诊次数中位数为7次)。通过调整混杂因素的线性和逻辑回归分析评估BPV与WMH负担及进展的关联。

结果

BPV与脑室周围WMH负担(β 0.36,95%CI 0.19 - 0.53,BPV每增加一个标准差)和皮质下(对数转换后)WMH相关(β 0.25,95%CI 0.08 - 0.42)。BPV与脑室周围(OR 1.09,95%CI 0.94 - 1.27)和皮质下WMH进展无关(OR 1.15,95%CI 0.99 - 1.35)。这些关联独立于平均血压。

结论

在缺血性脑卒中患者中,高就诊间BPV与皮质下和脑室周围WMH负担均相关,但在本研究中与WMH进展无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56f6/10827490/f1b41339d3a3/gr1.jpg

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