文献速递脑血管病认知障碍与痴呆

24小时血压变异性与中晚年认知及脑MRI结构改变标志物的关联

Association of 24-Hour Blood Pressure Variability With Cognition and Brain MRI Markers of Structural Change in Adults in Mid- to Late-Life.
PubMed 文献 · Neurology · 2026-04-30

基于澳大利亚BACH社区横断面研究(n=225,55-80岁无痴呆),24小时及清醒期血压变异性越高,整体认知与执行功能越差,且与血脑屏障水交换率降低相关;24小时血压变异性与白质高信号体积的关联仅见于APOE ε4携带者。HYPER研究(n=76)部分重复了睡眠期血压变异性与流体认知的负相关。

要点

  • 24小时和清醒期血压变异性升高与整体认知及执行功能较差相关。
  • 血压变异性升高与血脑屏障水交换率降低相关,提示屏障完整性受损。
  • APOE ε4携带者中24小时血压变异性与白质高信号体积正相关。

核心结论

  • 较高的24小时血压变异性与较差的整体认知和执行功能相关,并与血脑屏障完整性受损相关。
  • 24小时血压变异性与白质高信号体积的关联仅在APOE ε4携带者中观察到。
  • 血压变异性升高可能是加速脑老化的危险因素,尤其在APOE ε4携带者中。

研究设计与样本

  • BACH研究为社区横断面研究,纳入澳大利亚墨尔本55-80岁无痴呆参与者225人,完成24小时动态血压监测及医院评估。
  • 评估包括诊室血压、血液采集、神经心理测试和脑MRI,计算整体认知与执行功能复合评分。
  • HYPER研究用于部分重复动态血压与认知的关联,认知采用数字NIH Toolbox评估,纳入27-73岁参与者76人。
  • 线性回归模型调整人口学和血管危险因素,系数表示暴露每增加1个标准差时结局的标准差变化。

主要发现

  • BACH研究中,24小时血压变异性与整体认知负相关(β=-0.152,95%CI 0.278至-0.027),清醒期血压变异性与整体认知负相关(β=-0.158,95%CI -0.285至-0.031)。
  • 24小时血压变异性与执行功能负相关(β=-0.174,95%CI -0.299至-0.049),清醒期血压变异性与执行功能负相关(β=-0.168,95%CI -0.294至-0.042)。
  • 血压变异性与血脑屏障水交换率负相关(β=-0.180,95%CI -0.314至-0.045,n=213)。
  • 平均24小时血压与白质高信号负担正相关(β=0.182,95%CI 0.047-0.316,n=217)。
  • HYPER研究中,睡眠期血压变异性与流体认知负相关(β=-0.211,95%CI -0.382至-0.040)。

关键数值与推荐

  • BACH研究平均年龄67岁,女性占51%,n=225。
  • HYPER研究中位年龄63岁,女性占50%,n=76。
  • 24小时血压变异性与白质高信号体积的正相关仅在APOE ε4携带者中观察到。

临床怎么用

  • 对中晚年人群评估认知和脑白质健康时,可关注24小时动态血压监测中的血压变异性指标。
  • 对APOE ε4携带者,较高的24小时血压变异性可能提示更高的白质高信号负担风险。
  • 血压变异性升高或可作为加速脑老化的潜在风险标志,用于风险分层参考。

局限性

  • BACH研究为横断面设计,无法推断血压变异性与脑健康指标之间的因果关系。
  • HYPER研究样本量较小(n=76),仅部分重复了动态血压与认知的关联。

以上解读依据论文摘要(全文未开放获取或许可不允许翻译转载)。

原文

BACKGROUND AND OBJECTIVES: Blood pressure (BP) fluctuates across the 24-hour period. High 24-hour BP variability (BPV) is associated with cardiovascular disease risk, yet its relevance for brain health is unclear. We aimed to examine associations between 24-hour BPV, cognition, and multimodal MRI markers of brain health, and whether these were modified by APOE ε4 status. METHODS: In a cross-sectional study, dementia-free participants aged 55-80, from the community-based Brain and Cognitive Health (BACH) study in Melbourne, Australia, completed 24-hour ambulatory BP monitoring (ABPM) and hospital-based assessments: office BP, blood collection, neuropsychological testing, and brain MRI. ABPM variables included mean BP and coefficient of variation for 24-hour, awake, and asleep periods. Composites for global cognition and executive function were calculated. MRI markers included white matter hyperintensities (WMHs), brain volumetrics, cerebral blood flow, white matter free water, diffusion along the perivascular space, and blood-brain barrier water exchange rate. The primary outcomes were global cognition and WMH. We sought to partially replicate associations between ABPM and cognition in the HYpertension and gut PERmeability (HYPER) study, where cognition was assessed with the digital NIH Toolbox. Linear regressions were adjusted for demographic and vascular risk factors, with coefficients representing SD change in outcome per SD increase in exposure. RESULTS: In the BACH study (mean age = 67 years; 51% female; n = 225), higher 24-hour and awake BPV were associated with poorer global cognition (24-hour BPV: β = -0.152, 95% CI 0.278 to -0.027; awake BPV: -0.158, 95% CI -0.285 to -0.031) and executive function (24-hour BPV: β = -0.174, 95% CI-0.299 to -0.049; awake BPV: β = -0.168, 95% CI -0.294 to -0.042). BPV negatively associated with BBB kw (β = -0.180, 95% CI-0.314 to -0.045, n = 213). Mean 24-hour BP, positively associated with WMH burden (β = 0.182, 95% CI 0.047-0.316, n = 217). The 24-hour BPV positively associated with WMH volume among APOE ε4 carriers only. In HYPER (27-73 years, median age = 63 years; 50% female; n = 76), asleep BPV was negatively associated with fluid cognition (β = -0.211, 95% CI -0.382 to -0.040). DISCUSSION: Higher BPV was associated with poorer global cognition and executive functioning, and compromised blood-brain barrier integrity, with additional associations evident only among APOE ε4 carriers. Elevated BPV may be a risk factor for accelerated brain aging, particularly in APOE ε4 carriers.

来源:Neurology,查看原文。版权归原作者所有。

引用

  1. Gibson M, Snelson M, Rowsthorn E, et al. Association of 24-Hour Blood Pressure Variability With Cognition and Brain MRI Markers of Structural Change in Adults in Mid- to Late-Life. Neurology. 2026. PMID: 42060877. doi:10.1212/WNL.0000000000214935

供执业医师工作参考,不替代临床判断;数值与分级以指南原文为准。