Won Junyeon, Tomoto Tsubasa, Shan Kevin, Tarumi Takashi, Zhang Rong
Department of Neurology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Institute for Exercise and Environmental Medicine, Texas Health Presbyterian Hospital, Dallas, Texas, USA.
J Magn Reson Imaging. 2025 Jan 10. doi: 10.1002/jmri.29713.
Central arterial stiffening is associated with brain white matter (WM) damage and gray matter (GM) volume loss in older adults, but little is known about this association from an adult lifespan perspective.
To investigate the associations of central arterial stiffness with WM microstructural organization, WM lesion load, cortical thickness, and GM volume in healthy adults across the lifespan.
This is a cross-sectional study.
A total of 173 healthy adults (22-81 years) were included in this study.
FIELD STRENGTH/SEQUENCE: 3-T, T1-weighted magnetization prepared rapid gradient echo (MPRAGE), single-shot echo-planar imaging diffusion-weighted, and T2-weighted fluid-attenuated inversion recovery (FLAIR) sequences.
The participants underwent measurements of central arterial stiffness using carotid-femoral pulse wave velocity (cfPWV), diffusion tensor imaging (DTI) to measure whole-brain WM microstructural organization with free water (FW) and FW-corrected fractional anisotropy (FA), FLAIR to measure whole-brain WM hyperintensities (WMH), and MPRAGE to measure whole-brain cortical thickness and GM volume. The associations of age and cfPWV with MRI measures were assessed.
Linear regression models to examine the associations of brain WM and GM measures with age, cfPWV, and age × cfPWV interaction after adjusting for sex, education, and intracranial volume (ICV) (voxel-wise and cluster threshold P < 0.05). To understand the direction of the interaction result, the sample was stratified into lower and higher cfPWV groups using a median split of cfPWV.
Age × cfPWV interactions were observed in WM FW, WMH volume, cortical thickness, and GM volume (P < 0.01) such that the positive regression slopes between age, FW, and WMH volume were higher, while the negative regression slopes between age, cortical thickness, and GM volume were lower in those who had higher cfPWV relative to those who had lower cfPWV.
Central arterial stiffening may accelerate the age-related deteriorations in GM and WM structure across the adult lifespan.
Central arterial stiffening is associated with brain white matter (WM) damage and gray matter (GM) volume loss in older adults. We extended this investigation into an adult lifespan perspective by examining the associations of central arterial stiffening with brain structure in adults across age. A total of 172 healthy adults (22-81 years) underwent central arterial stiffening measure using applanation tonometry and brain measurement using MRI. We observed that higher central arterial stiffening may accelerate the age-related deterioration in brain WM and GM structure. These results suggest the importance of maintaining vascular health to slow age-related brain structural changes from an adult lifespan perspective.
4 TECHNICAL EFFICACY: Stage 5.
在老年人中,中心动脉僵硬度与脑白质(WM)损伤及灰质(GM)体积减少有关,但从成人一生的角度来看,这种关联鲜为人知。
探讨在整个成年期健康成年人中,中心动脉僵硬度与WM微观结构组织、WM病变负荷、皮质厚度及GM体积之间的关联。
这是一项横断面研究。
本研究共纳入173名健康成年人(22 - 81岁)。
场强/序列:3-T,T1加权磁化准备快速梯度回波(MPRAGE)序列、单次激发回波平面成像扩散加权序列以及T2加权液体衰减反转恢复(FLAIR)序列。
参与者接受了使用颈股脉搏波速度(cfPWV)测量中心动脉僵硬度、使用扩散张量成像(DTI)测量全脑WM微观结构组织(包括自由水(FW)和FW校正后的分数各向异性(FA))、使用FLAIR测量全脑WM高信号(WMH)以及使用MPRAGE测量全脑皮质厚度和GM体积。评估了年龄和cfPWV与MRI测量指标之间的关联。
采用线性回归模型,在调整性别、教育程度和颅内体积(ICV)后,检验脑WM和GM测量指标与年龄、cfPWV以及年龄×cfPWV交互作用之间的关联(体素水平和聚类阈值P < 0.05)。为了解交互作用结果的方向,根据cfPWV的中位数分割将样本分为cfPWV较低和较高两组。
在WM的FW、WMH体积、皮质厚度和GM体积方面观察到年龄×cfPWV交互作用(P < 0.01),即相对于cfPWV较低者,cfPWV较高者中年龄、FW和WMH体积之间的正回归斜率更高,而年龄、皮质厚度和GM体积之间的负回归斜率更低。
在整个成年期,中心动脉僵硬度可能会加速与年龄相关的GM和WM结构退化。
在老年人中中心动脉僵硬度与脑白质(WM)损伤和灰质(GM)体积减少有关。我们通过研究成年期不同年龄段成年人中心动脉僵硬度与脑结构的关联,将这一研究扩展到整个成年期视角。共有172名健康成年人(22 - 81岁)接受了使用压平眼压计测量中心动脉僵硬度以及使用MRI测量脑部的检查。我们观察到较高的中心动脉僵硬度可能会加速与年龄相关的脑WM和GM结构退化。这些结果表明,从成年期视角来看,维持血管健康对于减缓与年龄相关的脑结构变化具有重要意义。
4 技术效能:5级