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路易体痴呆症中的早期小胶质细胞激活和外周炎症。

Early microglial activation and peripheral inflammation in dementia with Lewy bodies.

机构信息

Department of Psychiatry, University of Cambridge, Cambridge, UK.

Sino-Britain Centre for Cognition and Ageing Research, Faculty of Psychology, Southwest University, Chongqing, China.

出版信息

Brain. 2018 Dec 1;141(12):3415-3427. doi: 10.1093/brain/awy265.

DOI:10.1093/brain/awy265
PMID:30403785
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6262214/
Abstract

Inflammation is increasingly recognized as part of the pathology of neurodegenerative conditions such as Alzheimer's disease and Parkinson's disease, but its role in dementia with Lewy bodies remains unclear. Using multimodal imaging and peripheral cytokine analysis, we therefore investigated central and peripheral inflammation in this common form of dementia. Nineteen participants with probable dementia with Lewy bodies and 16 similarly aged controls underwent 3 T MRI and PET imaging with 11C-PK11195, a marker of microglial activation in vivo. Peripheral blood inflammatory cytokines were also measured in all subjects, as well as in an additional 10 controls, using the Mesoscale Human Cytokine 36 plex panel and additional assays for high sensitivity c-reactive protein, tumour necrosis factor receptor 1, IL-34, YKL-40 (chitinase-3-like protein 1) and colony stimulating factor 1. To test for the presence of in vivo amyloid, 11C-Pittsburgh compound B PET imaging was also performed in 16 of the dementia with Lewy body participants. Microglial activation was elevated in dementia with Lewy bodies subjects with mild disease when compared to those with moderate/severe impairment, where disease severity was indexed by cognitive performance on the revised Addenbrooke's Cognitive Examination. In patients, strong correlations were found between cognitive performance and 11C-PK11195 non-displaceable binding potential in several regions including the caudate nucleus (R = 0.83, P = 0.00008) and cuneus (R = 0.77, P = 0.0005). Several inflammatory cytokines were altered in the patients compared to controls, with elevated macrophage inflammatory protein-3 (P = 0.001), IL-17A (P = 0.008) and IL-2 (P = 0.046) and reduced IL-8 (P = 0.024). There was no correlation between cortical 11C-Pittsburgh compound B standardized uptake value ratio and clinical features, regional 11C-PK11195 binding or peripheral cytokine levels. Nor was there any regional correlation between 11C-PK11195 non-displaceable binding potentials and 11C-Pittsburgh compound B standardized uptake value ratios. Our findings provide evidence for both central and peripheral inflammatory changes in dementia with Lewy bodies, with microglial activation occurring early in the disease in key regions known to be associated with pathology, before declining as cognition declines. Raised peripheral cytokines associated with T cell function further suggest a role for the adaptive immune system in the pathogenesis of the disease.

摘要

炎症越来越被认为是阿尔茨海默病和帕金森病等神经退行性疾病病理的一部分,但它在路易体痴呆中的作用仍不清楚。因此,我们使用多模态成像和外周细胞因子分析来研究这种常见形式痴呆症的中枢和外周炎症。19 名可能患有路易体痴呆的参与者和 16 名年龄相似的对照者接受了 3T MRI 和 11C-PK11195 的 PET 成像,11C-PK11195 是体内小胶质细胞激活的标志物。所有受试者均测量了外周血炎性细胞因子,另外 10 名对照者还使用 Mesoscale Human Cytokine 36 plex 面板和高灵敏度 C 反应蛋白、肿瘤坏死因子受体 1、IL-34、YKL-40(几丁质酶-3 样蛋白 1)和集落刺激因子 1 的其他检测方法进行了测量。为了检测体内淀粉样蛋白的存在,16 名路易体痴呆患者还进行了 11C-匹兹堡化合物 B PET 成像。与认知表现中度/重度受损的患者相比,轻度疾病的路易体痴呆患者的小胶质细胞激活升高,其中疾病严重程度由改良的 Addenbrooke 认知测验评估的认知表现来衡量。在患者中,在包括尾状核(R = 0.83,P = 0.00008)和楔前叶(R = 0.77,P = 0.0005)在内的几个区域中,发现认知表现与 11C-PK11195 不可置换结合潜能之间存在很强的相关性。与对照组相比,患者的几种炎性细胞因子发生了改变,其中巨噬细胞炎性蛋白-3(P = 0.001)、IL-17A(P = 0.008)和 IL-2(P = 0.046)升高,IL-8(P = 0.024)降低。皮质 11C-匹兹堡化合物 B 标准化摄取值比与临床特征、区域 11C-PK11195 结合或外周细胞因子水平之间没有相关性。11C-PK11195 不可置换结合潜能与 11C-匹兹堡化合物 B 标准化摄取值比之间也没有区域相关性。我们的研究结果为路易体痴呆症中的中枢和外周炎症变化提供了证据,在与病理相关的关键区域,小胶质细胞激活在疾病早期发生,随后随着认知能力下降而下降。与 T 细胞功能相关的外周细胞因子升高进一步表明适应性免疫系统在疾病发病机制中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd9/6262214/32a252de2b7a/awy265f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd9/6262214/ca9d83d73ec7/awy265f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd9/6262214/d10eff604487/awy265f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd9/6262214/735e6166ec9a/awy265f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd9/6262214/7adf15976097/awy265f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd9/6262214/32a252de2b7a/awy265f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd9/6262214/ca9d83d73ec7/awy265f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd9/6262214/d10eff604487/awy265f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd9/6262214/735e6166ec9a/awy265f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd9/6262214/7adf15976097/awy265f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd9/6262214/32a252de2b7a/awy265f5.jpg

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