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Cholinesterase inhibitors and beyond.胆碱酯酶抑制剂及其他。
Curr Alzheimer Res. 2009 Apr;6(2):86-96. doi: 10.2174/156720509787602861.
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Cerebrospinal fluid biomarker signature in Alzheimer's disease neuroimaging initiative subjects.阿尔茨海默病神经影像学计划受试者的脑脊液生物标志物特征
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Recent developments in Alzheimer's disease therapeutics.阿尔茨海默病治疗学的最新进展。
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S100A7, a novel Alzheimer's disease biomarker with non-amyloidogenic alpha-secretase activity acts via selective promotion of ADAM-10.S100A7是一种具有非淀粉样前体蛋白生成性α-分泌酶活性的新型阿尔茨海默病生物标志物,其通过选择性促进ADAM-10发挥作用。
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MicroRNA regulation of Alzheimer's Amyloid precursor protein expression.微小RNA对阿尔茨海默病淀粉样前体蛋白表达的调控
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Biological imaging in radiation therapy: role of positron emission tomography.放射治疗中的生物成像:正电子发射断层扫描的作用
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症状性和无症状性患者的阿尔茨海默病生物标志物发现:实验方法和未来的临床应用。

Alzheimer's disease biomarker discovery in symptomatic and asymptomatic patients: experimental approaches and future clinical applications.

机构信息

Center of Excellence for Novel Approaches to Neurodiagnostics and Neurotherapeutics, Brain Institute, and Center of Excellence in Complementary and Alternative Medicine in Alzheimer's Disease, Department of Neurology, Mount Sinai School of Medicine, 1 Gustave L. Levy Place, Box 1137, New York, NY 10029, USA.

出版信息

Exp Gerontol. 2010 Jan;45(1):15-22. doi: 10.1016/j.exger.2009.09.007. Epub 2009 Sep 29.

DOI:10.1016/j.exger.2009.09.007
PMID:19796674
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2840994/
Abstract

Alzheimer's disease (AD) is the most common form of dementia in the elderly. Current treatments for AD are not as effective as needed, nor is there any definitive antemortem diagnostic. Understanding the biological processes that occur during AD onset and/or progression will improve disease diagnosis and treatment. Recent applications of microarray technologies for analysis of messenger (m) RNA expression profiles have elucidated distinct changes in the brain as a function of AD dementia initiation and progression. However, mRNA analysis underestimates post-transcriptional modifications and therefore provides only a partial view of the molecular changes in the AD brain. Combining mRNA studies with protein expression analysis may provide a more global picture of the biological processes associated with AD dementia. Information gathered could lead to the development of select biological indices (biomarkers) for guiding AD diagnosis and therapy. We will provide a brief background on AD, followed by a review on the applications of microarray, proteomics, as well as microRNA expression profile analysis to develop novel diagnostic strategies that may be useful for the diagnosis AD and for monitoring disease progression. The availability of biomarkers that promote early disease diagnosis, particularly among asymptomatic patients, will lead to the application of personalized medicine in AD.

摘要

阿尔茨海默病(AD)是老年人中最常见的痴呆症形式。目前 AD 的治疗方法并不像需要的那样有效,也没有明确的生前诊断方法。了解 AD 发病和/或进展过程中发生的生物学过程将改善疾病的诊断和治疗。最近应用微阵列技术分析信使(m)RNA 表达谱,阐明了 AD 痴呆症起始和进展过程中大脑的明显变化。然而,mRNA 分析低估了转录后修饰,因此仅提供了 AD 大脑中分子变化的部分视图。将 mRNA 研究与蛋白质表达分析相结合,可能为与 AD 痴呆症相关的生物学过程提供更全面的认识。收集的信息可能会导致选择生物指标(生物标志物)的发展,以指导 AD 的诊断和治疗。我们将简要介绍 AD 的背景,然后回顾微阵列、蛋白质组学以及 microRNA 表达谱分析的应用,以开发新的诊断策略,这些策略可能有助于 AD 的诊断,并监测疾病的进展。促进早期疾病诊断的生物标志物的出现,特别是在无症状患者中,将导致 AD 中个性化医疗的应用。