路易体痴呆患者皮层微结构异常及其与阿尔茨海默病病理的关系

IF 6.7 1区 医学 Q1 NEUROSCIENCES
Elijah Mak, Robert I. Reid, Scott A. Przybelski, Angela M. Fought, Timothy G. Lesnick, Christopher G. Schwarz, Matthew L. Senjem, Sheelakumari Raghavan, Prashanthi Vemuri, Clifford R. Jack, Hoon Ki Min, Manoj K. Jain, Toji Miyagawa, Leah K. Forsberg, Julie A. Fields, Rodolfo Savica, Jonathan Graff-Radford, David T. Jones, Hugo Botha, Erik K. St. Louis, David S. Knopman, Vijay K. Ramanan, Dennis W. Dickson, Neill R. Graff-Radford, Gregory S. Day, Tanis J. Ferman, Ronald C. Petersen, Val J. Lowe, Bradley F. Boeve, John T. O’Brien, Kejal Kantarci
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引用次数: 0

摘要

路易体痴呆(DLB)经常与阿尔茨海默病病理共存,但皮层微结构损伤的模式及其与淀粉样蛋白、tau蛋白和脑血管病理的关系尚不清楚。我们通过量化平均扩散率(MD)、组织加权神经突密度指数(tNDI)、定向分散指数(ODI)和游离水分数(FWF),应用神经突定向分散和密度成像(NODDI)评估了57名DLB患者和57名年龄和性别匹配的认知未受损对照组的皮层显微结构完整性。使用PiB和Flortaucipir PET成像测量淀粉样蛋白和tau蛋白水平。与对照组相比,DLB表现出MD和FWF增加,跨多个区域的tNDI减少,枕皮质局灶性ODI减少。结构方程模型显示,APOE基因型影响淀粉样蛋白水平,从而升高tau蛋白,导致微结构损伤。这些发现强调了AD病理在DLB神经退行性变中的作用,提倡针对AD和DLB特异性病理的多靶点治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cortical microstructural abnormalities in dementia with Lewy bodies and their associations with Alzheimer’s disease copathologies

Cortical microstructural abnormalities in dementia with Lewy bodies and their associations with Alzheimer’s disease copathologies

Dementia with Lewy bodies (DLB) frequently coexists with Alzheimer’s disease pathology, yet the pattern of cortical microstructural injury and its relationship with amyloid, tau, and cerebrovascular pathologies remains unclear. We applied neurite orientation dispersion and density imaging (NODDI) to assess cortical microstructural integrity in 57 individuals within the DLB spectrum and 57 age- and sex-matched cognitively unimpaired controls by quantifying mean diffusivity (MD), tissue-weighted neurite density index (tNDI), orientation dispersion index (ODI), and free water fraction (FWF). Amyloid and tau levels were measured using PiB and Flortaucipir PET imaging. Compared to controls, DLB exhibited increased MD and FWF, reduced tNDI across multiple regions, and focal ODI reductions in the occipital cortex. Structural equation modeling revealed that APOE genotype influenced amyloid levels, which elevated tau, leading to microstructural injury. These findings highlight the role of AD pathology in DLB neurodegeneration, advocating for multi-target therapeutic approaches addressing both AD and DLB-specific pathologies.

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来源期刊
NPJ Parkinson's Disease
NPJ Parkinson's Disease Medicine-Neurology (clinical)
CiteScore
9.80
自引率
5.70%
发文量
156
审稿时长
11 weeks
期刊介绍: npj Parkinson's Disease is a comprehensive open access journal that covers a wide range of research areas related to Parkinson's disease. It publishes original studies in basic science, translational research, and clinical investigations. The journal is dedicated to advancing our understanding of Parkinson's disease by exploring various aspects such as anatomy, etiology, genetics, cellular and molecular physiology, neurophysiology, epidemiology, and therapeutic development. By providing free and immediate access to the scientific and Parkinson's disease community, npj Parkinson's Disease promotes collaboration and knowledge sharing among researchers and healthcare professionals.
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