Association of MRI Indices of Glymphatic System With Amyloid Deposition and Cognition in Mild Cognitive Impairment and Alzheimer Disease

淋巴系统 标准摄取值 血管周围间隙 匹兹堡化合物B 医学 白质 阿尔茨海默病 内科学 认知功能衰退 病理 混淆 心理学 神经影像学 痴呆 磁共振成像 心脏病学 疾病 核医学 正电子发射断层摄影术 脑脊液 放射科 精神科
作者
Koji Kamagata,Christina Andica,Kaito Takabayashi,Yuya Saito,Toshiaki Taoka,Hayato Nozaki,Junko Kikuta,Shohei Fujita,Akifumi Hagiwara,Kouhei Kamiya,Akihiko Wada,Toshiaki Akashi,Katsuhiro Sano,Mitsuo Nishizawa,Masaaki Hori,Shinji Naganawa,Shigeki Aoki
出处
期刊:Neurology [Ovid Technologies (Wolters Kluwer)]
卷期号:99 (24) 被引量:119
标识
DOI:10.1212/wnl.0000000000201300
摘要

Background and Objectives

The glymphatic system is a whole-brain perivascular network, which promotes CSF/interstitial fluid exchange. Alterations to this system may play a pivotal role in amyloid β (Aβ) accumulation. However, its involvement in Alzheimer disease (AD) pathogenesis is not fully understood. Here, we investigated the changes in noninvasive MRI measurements related to the perivascular network in patients with mild cognitive impairment (MCI) and AD. Additionally, we explored the associations of MRI measures with neuropsychological score, PET standardized uptake value ratio (SUVR), and Aβ deposition.

Methods

MRI measures, including perivascular space (PVS) volume fraction (PVSVF), fractional volume of free water in white matter (FW-WM), and index of diffusivity along the perivascular space (ALPS index) of patients with MCI, those with AD, and healthy controls from the Alzheimer9s Disease Neuroimaging Initiative database were compared. MRI measures were also correlated with the levels of CSF biomarkers, PET SUVR, and cognitive score in the combined subcohort of patients with MCI and AD. Statistical analyses were performed with age, sex, years of education, and APOE status as confounding factors.

Results

In total, 36 patients with AD, 44 patients with MCI, and 31 healthy controls were analyzed. Patients with AD had significantly higher total, WM, and basal ganglia PVSVF (Cohen d = 1.15–1.48; p < 0.001) and FW-WM (Cohen d = 0.73; p < 0.05) and a lower ALPS index (Cohen d = 0.63; p < 0.05) than healthy controls. Meanwhile, the MCI group only showed significantly higher total (Cohen d = 0.99; p < 0.05) and WM (Cohen d = 0.91; p < 0.05) PVSVF. Low ALPS index was associated with lower CSF Aβ42 (rs = 0.41, pfdr = 0.026), FDG-PET uptake (rs = 0.54, pfdr < 0.001), and worse multiple cognitive domain deficits. High FW-WM was also associated with lower CSF Aβ42 (rs = −0.47, pfdr = 0.021) and worse cognitive performances.

Discussion

Our study indicates that changes in PVS-related MRI parameters occur in MCI and AD, possibly due to impairment of the glymphatic system. We also report the associations between MRI parameters and Aβ deposition, neuronal change, and cognitive impairment in AD.
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