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阿尔茨海默病患者的脑脊液脂质介质特征。

Cerebrospinal Fluid Profile of Lipid Mediators in Alzheimer's Disease.

机构信息

Neuroscience Center of Excellence, School of Medicine, Louisiana State University Health New Orleans, 2020 Gravier Street, Suite D, New Orleans, LA, 70112, USA.

Faculty of Medicine, PHENIKAA University, Hanoi, 12116, Vietnam.

出版信息

Cell Mol Neurobiol. 2023 Mar;43(2):797-811. doi: 10.1007/s10571-022-01216-5. Epub 2022 Apr 1.

Abstract

Alzheimer's disease (AD) develops into dementia over a period of several years, during which subjective cognitive impairment (SCI) and mild cognitive impairment (MCI) can be used as intermediary diagnoses of increasing severity. Chronic neuroinflammation resulting from insufficient resolution is involved in the pathogenesis of AD and is associated with cognitive impairment. Specialized pro-resolving lipid mediators (LMs) that promote the resolution of inflammation may be valuable markers in AD diagnosis and as therapeutic targets. Liquid chromatography-tandem mass spectrometry was used to analyze pro-resolving and pro-inflammatory LMs in cerebrospinal fluid (CSF) from patients with cognitive impairment ranging from subjective impairment to a diagnosis of AD and correlated to cognition, CSF tau, and β-amyloid. Resolvin (Rv) D4, RvD1, neuroprotectin D1 (NPD1), maresin 1 (MaR1), and RvE4 were lower in AD and/or MCI compared to SCI. The pro-inflammatory LTB and 15-HETE were higher in AD and MCI, respectively, while PGD2, PGE2, and PGF2a were decreased in AD, compared to SCI. RvD4 was also negatively correlated to AD tangle biomarkers, and positive correlations to cognitive test scores were observed for both pro-resolving LMs and their precursor fatty acids. In this exploratory study of the lipidome in CSF of AD, MCI, and SCI, the results indicate a shift in the LM profile from pro-resolving to pro-inflammatory in progression to AD, suggesting that it may be of use as a biomarker when followed by confirmation by replication studies.

摘要

阿尔茨海默病(AD)在数年的时间里发展为痴呆,在此期间,主观认知障碍(SCI)和轻度认知障碍(MCI)可作为病情加重的中间诊断。由于解决不充分而导致的慢性神经炎症参与了 AD 的发病机制,并与认知障碍有关。促进炎症解决的专门的促解决脂质介质(LM)可能是 AD 诊断和治疗靶点的有价值的标志物。采用液相色谱-串联质谱法分析了从主观障碍到 AD 诊断的认知障碍患者的脑脊液(CSF)中的促解决和促炎 LM,并与认知、CSF 中的 tau 和 β-淀粉样蛋白相关联。与 SCI 相比,AD 和/或 MCI 中 RvD4、RvD1、神经保护素 D1(NPD1)、maresin 1(MaR1)和 RvE4 降低。AD 和 MCI 中促炎的 LTB 和 15-HETE 分别升高,而与 SCI 相比,AD 中 PGD2、PGE2 和 PGF2a 降低。RvD4 也与 AD 缠结生物标志物呈负相关,而促解决 LM 及其前体脂肪酸与认知测试评分呈正相关。在 AD、MCI 和 SCI 的 CSF 脂质组学的这项探索性研究中,结果表明 LM 谱从解决向 AD 进展中向促炎转变,表明它可能在通过复制研究进行确认后作为生物标志物使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f352/11415155/9aa6e4f92407/10571_2022_1216_Fig1_HTML.jpg

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