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皮质类固醇,但不是 NSAIDs,与较少的阿尔茨海默病神经病理学有关。

Corticosteroids, but not NSAIDs, are associated with less Alzheimer neuropathology.

机构信息

Department of Psychiatry, The Mount Sinai School of Medicine, New York, NY 10029, USA.

出版信息

Neurobiol Aging. 2012 Jul;33(7):1258-64. doi: 10.1016/j.neurobiolaging.2011.02.011. Epub 2011 Apr 1.

DOI:10.1016/j.neurobiolaging.2011.02.011
PMID:21458888
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3130103/
Abstract

The objective of this study was to test the hypothesis that corticosteroid and nonsteroidal anti-inflammatory drug (NSAID) medications are associated with less global and regional Alzheimer's disease (AD) neuropathology. This postmortem study was based on 694 brains of subjects from the Mount Sinai School of Medicine Brain Bank who did not have neuropathologies other than neuritic plaques (NPs), neurofibrillary tangles (NFTs), or cerebrovascular disease. Densities of NPs and of NFTs were assessed in several neocortical regions and in the hippocampus, entorhinal cortex, and amygdala. Counts of NPs in several neocortical regions were also assessed. For each neuropathology measure, analyses of covariance controlling for age at death and sex compared subjects who received only corticosteroids (n = 54) or those who received only NSAIDs (n = 56) to the same comparison group, subjects who received neither (n = 576). Subjects receiving corticosteroids had significantly lower ratings and counts of NPs for all neuropathological measures, and NFTs overall and in the cerebral cortex and amygdala. In contrast, no measures were significant for subjects who received NSAIDs. Use of corticosteroids was associated with approximately 50% fewer NPs and NFTs in most brain regions examined, compared with nonmedicated subjects. In contrast, use of NSAIDs was not substantially associated with the reductions in hallmark lesions of AD. Because corticosteroids have anti-inflammatory as well as a myriad of other neurobiological effects, more direct studies in model systems could reveal novel therapeutic targets and mechanisms for AD lesion reduction.

摘要

本研究旨在验证以下假设,即皮质类固醇和非甾体抗炎药(NSAID)与较少的全脑和区域性阿尔茨海默病(AD)神经病理学相关。这项尸检研究基于西奈山医学院脑库的 694 名受试者的大脑,这些受试者除神经纤维缠结(NFTs)、神经原纤维缠结(NFTs)或脑血管病外,没有其他神经病理学。评估了几个新皮质区域和海马体、内嗅皮层和杏仁核中的神经斑块(NPs)和 NFTs 的密度。还评估了几个新皮质区域的 NPs 计数。对于每种神经病理学测量,通过协方差分析控制死亡时的年龄和性别,将仅接受皮质类固醇(n = 54)或仅接受 NSAID(n = 56)的受试者与相同的比较组(n = 576)进行比较。接受皮质类固醇治疗的受试者在所有神经病理学测量中,NP 的评分和计数均显著降低,并且 NFTs 在大脑皮层和杏仁核中也显著降低。相比之下,接受 NSAID 治疗的受试者没有任何测量结果显著。与未用药受试者相比,接受皮质类固醇治疗的受试者在大多数检查的大脑区域中,NP 和 NFT 的数量减少了约 50%。相比之下,NSAID 的使用与 AD 标志性病变的减少没有明显关联。由于皮质类固醇具有抗炎作用以及无数其他神经生物学作用,因此在模型系统中进行更直接的研究可能会揭示 AD 病变减少的新治疗靶点和机制。

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