White matter structure-function coupling alteration is associated with plasma biomarkers and cognition in Alzheimer's disease.

IF 4.7 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Yihao Guo, Tao Liu, Huijuan Chen, Weiyuan Huang, Kun Zhang, Feng Chen
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引用次数: 0

Abstract

Objectives: There were white matter (WM) microstructural abnormalities in Alzheimer's disease (AD), and it may affect information transmission along WM tracts. We aim to investigate AD-related changes in the structure-function coupling of WM and their associations with AD plasma biomarkers and cognitive performance.

Methods: This retrospective study evaluated participants who provided blood samples, underwent MR brain scans, and completed neuropsychological assessments. Plasma biomarker levels of β-amyloid (Aβ), phosphorylated tau181 (p-tau181), glial fibrillary acidic protein (GFAP), and neurofilament light chain (NfL) were measured using the Single Molecule Array platform. We used a structure-function coupling approach, combining spatial-temporal correlations of functional signals with diffusion tensor orientations in the WM circuit derived from functional and diffusion magnetic resonance imaging (MRI). Association and mediation analyses were conducted to explore the relationships among plasma biomarkers, structure-function coupling, and cognitive performance in AD.

Results: Compared with the cognitively normal (CN) and mild cognitive impairment (MCI) groups, the AD dementia group showed a widespread increase in structure-function coupling within WM regions, including the body and splenium of the corpus callosum. Additionally, structure-function coupling in WM tracts was significantly associated with the levels of p-tau181 and NfL. Moreover, structure-function coupling mediated the relationship between memory and the level of p-tau181 or NfL.

Conclusion: Our findings suggest that there is altered information transmission along WM tracts in patients with AD. The brain structure-function coupling is associated with plasma biomarkers and cognitive scores, suggesting that abnormal signal transfer of neuronal fiber pathways could be a potential mechanism of AD neuropathology.

Key points: Question White matter (WM) microstructural abnormalities may affect information transmission along WM tracts, resulting in cognitive decline in Alzheimer's disease (AD). Findings The AD dementia group showed a widespread increase in structure-function coupling within WM regions, which was associated with plasma biomarkers and cognitive scores. Clinical relevance The brain structure-function coupling is associated with plasma biomarkers and cognitive scores, suggesting that abnormal signal transfer of neuronal fiber pathways could be a potential mechanism of the neuropathology of AD.

白质结构-功能耦合改变与阿尔茨海默病的血浆生物标志物和认知相关。
目的:阿尔茨海默病(AD)患者存在白质(WM)微结构异常,其可能影响信息沿白质束的传递。我们的目的是研究AD相关的WM结构-功能耦合变化及其与AD血浆生物标志物和认知表现的关系。方法:这项回顾性研究评估了提供血液样本、接受MR脑部扫描和完成神经心理学评估的参与者。利用单分子阵列平台检测血浆β-淀粉样蛋白(Aβ)、磷酸化tau181 (p-tau181)、胶质纤维酸性蛋白(GFAP)和神经丝轻链(NfL)的生物标志物水平。我们使用了结构-功能耦合方法,将功能信号的时空相关性与WM电路中来自功能和扩散磁共振成像(MRI)的扩散张量方向结合起来。通过关联和中介分析来探讨血浆生物标志物、结构-功能耦合和AD认知表现之间的关系。结果:与认知正常(CN)和轻度认知障碍(MCI)组相比,AD痴呆组在包括胼胝体体和脾在内的WM区域显示出广泛的结构-功能耦合增加。此外,WM束的结构-功能耦合与p-tau181和NfL的水平显著相关。此外,结构-功能耦合介导了记忆与p-tau181或NfL水平之间的关系。结论:我们的研究结果表明,AD患者WM束的信息传递发生了改变。脑结构-功能耦合与血浆生物标志物和认知评分相关,提示神经元纤维通路的异常信号传递可能是AD神经病理的潜在机制。白质(WM)微结构异常可能影响WM束的信息传递,导致阿尔茨海默病(AD)的认知能力下降。AD痴呆组显示WM区域结构-功能耦合广泛增加,这与血浆生物标志物和认知评分相关。脑结构-功能耦合与血浆生物标志物和认知评分相关,提示神经元纤维通路的异常信号传递可能是AD神经病理的潜在机制。
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来源期刊
European Radiology
European Radiology 医学-核医学
CiteScore
11.60
自引率
8.50%
发文量
874
审稿时长
2-4 weeks
期刊介绍: European Radiology (ER) continuously updates scientific knowledge in radiology by publication of strong original articles and state-of-the-art reviews written by leading radiologists. A well balanced combination of review articles, original papers, short communications from European radiological congresses and information on society matters makes ER an indispensable source for current information in this field. This is the Journal of the European Society of Radiology, and the official journal of a number of societies. From 2004-2008 supplements to European Radiology were published under its companion, European Radiology Supplements, ISSN 1613-3749.
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