Department of Neurology (M.B.M., S.M., S. Sedaghat, P.B.G., F.A.S.), Northwestern University, Chicago, IL.
Institute for Public Health and Medicine (M.B.M., D.M.L.-J.), Northwestern University, Chicago, IL.
Hypertension. 2024 Sep;81(9):1935-1944. doi: 10.1161/HYPERTENSIONAHA.123.22824. Epub 2024 Jul 23.
Vascular risk factors, particularly hypertension, are important contributors to accelerated brain aging. We sought to quantify vascular risk factor risks over adulthood and assess the empirical evidence for risk thresholds.
We used SBP (systolic blood pressure) and diastolic blood pressure, total cholesterol, fasting blood glucose, and body mass index measurements collected from participants in the CARDIA study (Coronary Artery Risk Development in Young Adults) at 2- to 5-year intervals through year 30. The Montreal Cognitive Assessment and domain-specific cognitive tests were performed at year 30. White matter hyperintensity volume was measured by magnetic resonance imaging. We used a 2-step method to fit longitudinal vascular risk factor exposures to optimized spline functions with mixed-effects models, then used the participant-specific random effects that characterized individual exposures over time in cross-sectional models adjusted for sex, race, age, and education to study effects on midlife brain health.
Change in SBP up to 33 years of age was negatively associated with Montreal Cognitive Assessment scores (-0.29 Montreal Cognitive Assessment score per mm Hg/y change [95% CI, -0.49 to -0.09]; =0.005), with similar effects for SBP changes from 33 to 49 years of age (-0.08 [95% CI, -0.16 to 0.01]; =0.08). We observed comparable, significant associations between SBP exposure during those ages, midlife performance on specific cognitive domains, and volume of white matter hyperintensity (all <0.05). SBP ≤111 mm Hg was the estimated threshold below which no harmful association with midlife cognitive performance was identified.
SBP in early adulthood is the vascular risk factor most strongly associated with midlife cognitive performance and white matter hyperintensity burden, with SBP 111 mm Hg suggested as a harm threshold.
血管危险因素,特别是高血压,是导致大脑加速老化的重要因素。我们旨在量化成年期血管危险因素的风险,并评估风险阈值的经验证据。
我们使用 SBP(收缩压)和舒张压、总胆固醇、空腹血糖和体重指数,这些数据是通过 CARDIA 研究(年轻人冠状动脉风险发展)收集的,参与者在 2 到 5 年的时间间隔内进行测量,直至 30 岁。在 30 岁时进行蒙特利尔认知评估和特定领域的认知测试。通过磁共振成像测量脑白质高信号体积。我们使用两步法,通过混合效应模型将纵向血管危险因素暴露拟合到优化的样条函数,然后使用参与者特定的随机效应来描述个体在时间上的暴露情况,在调整性别、种族、年龄和教育的横断面模型中研究对中年大脑健康的影响。
33 岁前的 SBP 变化与蒙特利尔认知评估评分呈负相关(每毫米汞柱/年变化 0.29 个蒙特利尔认知评估评分[-0.49 至 -0.09];=0.005),33 至 49 岁之间的 SBP 变化也有类似的影响(-0.08 [95%CI,-0.16 至 0.01];=0.08)。我们观察到在这些年龄段期间 SBP 暴露与中年特定认知领域的表现以及脑白质高信号体积之间存在类似的显著关联(均<0.05)。SBP≤111mmHg 被估计为没有与中年认知表现发生有害关联的阈值。
成年早期的 SBP 与中年认知表现和脑白质高信号负担的相关性最强,SBP 111mmHg 被认为是一个危害阈值。