Laboratory of NeuroImaging, USC Stevens Neuroimaging and Informatics Institute, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA; Alzheimer's Disease Research Center, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Laboratory of NeuroImaging, USC Stevens Neuroimaging and Informatics Institute, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA; Neuroscience Graduate Program, University of Southern California, Los Angeles, CA, USA.
Neurobiol Aging. 2021 Mar;99:28-43. doi: 10.1016/j.neurobiolaging.2020.12.010. Epub 2020 Dec 16.
Vascular contributions to early cognitive decline are increasingly recognized, prompting further investigation into the nature of related changes in perivascular spaces (PVS). Using magnetic resonance imaging, we show that, compared to a cognitively normal sample, individuals with early cognitive dysfunction have altered PVS presence and distribution, irrespective of Amyloid-β. Surprisingly, we noted lower PVS presence in the anterosuperior medial temporal lobe (asMTL) (1.29 times lower PVS volume fraction in cognitively impaired individuals, p < 0.0001), which was associated with entorhinal neurofibrillary tau tangle deposition (beta (standard error) = -0.98 (0.4); p = 0.014), one of the hallmarks of early Alzheimer's disease pathology. We also observed higher PVS volume fraction in centrum semi-ovale of the white matter, but only in female participants (1.47 times higher PVS volume fraction in cognitively impaired individuals, p = 0.0011). We also observed PVS changes in participants with history of hypertension (higher in the white matter and lower in the asMTL). Our results suggest that anatomically specific alteration of the PVS is an early neuroimaging feature of cognitive impairment in aging adults, which is differentially manifested in female.
血管对早期认知衰退的影响越来越受到重视,促使人们进一步研究与血管周围间隙(PVS)相关的变化性质。我们使用磁共振成像技术表明,与认知正常的样本相比,早期认知功能障碍患者的 PVS 存在和分布发生了改变,而与淀粉样蛋白-β无关。令人惊讶的是,我们注意到在前上内侧颞叶(asMTL)中 PVS 的存在较低(认知障碍个体的 PVS 体积分数低 1.29 倍,p<0.0001),这与内嗅皮层神经纤维缠结tau 沉积有关(beta(标准误差)=-0.98(0.4);p=0.014),这是早期阿尔茨海默病病理的标志之一。我们还观察到脑白质半卵圆中心的 PVS 体积分数较高,但仅在女性参与者中(认知障碍个体的 PVS 体积分数高 1.47 倍,p=0.0011)。我们还观察到有高血压病史的参与者的 PVS 变化(脑白质中较高,asMTL 中较低)。我们的研究结果表明,PVS 的解剖学特异性改变是老年认知障碍的早期神经影像学特征,在女性中表现出不同的特征。