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Assessment of diffusivity along the perivascular space in early- and late-onset Alzheimer's disease

血管周围间隙 疾病 早发性阿尔茨海默病 阿尔茨海默病 空格(标点符号) 热扩散率 心理学 神经科学 医学 病理 哲学 物理 语言学 量子力学
作者
Xiao Luo,Hui Hong,Shuyue Wang,Kaicheng Li,Qingze Zeng,X B Liu,Luwei Hong,Jixuan Li,Xinyi Zhang,Siyan Zhong,Lingyun Liu,Chao Wang,Yanxing Chen,Minming Zhang,Peiyu Huang
出处
期刊:Journal of Alzheimer's Disease [IOS Press]
标识
DOI:10.1177/13872877251360416
摘要

BackgroundCerebrospinal fluid (CSF) dynamics plays a key role in clearing soluble amyloid-β from the brain, which may impact Alzheimer's disease (AD) onset.ObjectiveThis study seeks to differentiate cerebrospinal fluid dysfunction between early-onset AD (EOAD) and late-onset AD (LOAD) subtypes and to examine their associations with brain changes and cognitive function.MethodsWe performed in vivo imaging measurements on 40 EOAD patients, 38 LOAD patients, 69 age-matched young normal controls (YNC), and 60 old normal controls (ONC). Measured variables included diffusion tensor imaging along the perivascular space (DTI-ALPS, subdivided into left, right, and mean), amyloid and tau PET standardized uptake value ratios (SUVR), hippocampus volume, and white matter hyperintensities (WMH) volume. For normally distributed variables, we used ANOVA to assess group differences, followed by Tukey's HSD test for multiple comparison correction. Results without correction are marked. Pearson correlation and linear regression analyzed relationships between the DTI-ALPS index, brain parameters, and cognition within each subgroup.ResultsBoth EOAD (p < 0.05, uncorrected) and LOAD (p < 0.05, corrected) showed a lower DTI-ALPS index compared to controls. This lower index was associated with increased disease severity and worsening cognitive performance. In EOAD, the lower DTI-ALPS index was primarily linked to amyloid (Std beta = -0.463, p = 0.008), while in LOAD, it was predominantly associated with age (Std beta = -0.348, p = 0.006) and WMH (Std beta = -0.330, p = 0.009).ConclusionsThis observation suggests that differences in the etiology of cerebrospinal fluid dysfunction may exist between these AD subtypes, warranting further investigation to confirm these hypotheses.
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