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CSF Biomarkers

机译:脑脊液生物标志物

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摘要

With an ever growing population of aged individuals who are at risk of developing Alzheimer's disease (AD), there is an urgent need for a sensitive, specific and preferably non-invasive diagnostic standard of disease progression. Diagnosis of AD is still largely based on exclusion criteria of secondary causes and other forms of dementia with similar clinical pictures, than the diagnostic accuracy of AD is low. Recent research focused the attention to biochemical diagnostic markers (biomarkers) as they are very important indicators of normal and abnormal biological processes. Molecular aberrations in the AD brain are reflected in the cerebrospinal fluid (CSF) where three candidate biomarkers have recently been identified: total tau protein, amyloid β-protein 1-42 and tau protein phosphorylated at AD-specific epitopes. The sensitivity and specificity of these data are able for discrimination of AD patients from controls. Here, we review the recent literature on biochemical biomarkers and discuss their predictive value as indicative for disease vulnerability to detect individuals at risk for AD and to determine the clinical efficacy of novel, disease-modifying strategies. According to the literature analysis reported in the present review, we can conclude that the combination of the CSF biomarkers and their ratios may significantly increase the specificity and the accuracy of AD diagnosis.
机译:随着具有发展为阿尔茨海默氏病(AD)风险的老年个体的不断增长,迫切需要疾病发展的敏感,特异性和优选非侵入性诊断标准。 AD的诊断仍主要基于继发原因和其他形式的痴呆且具有相似临床表现的排除标准,因为AD的诊断准确性较低。最近的研究将注意力集中在生化诊断标记物(biomarkers)上,因为它们是正常和异常生物学过程的非常重要的指标。 AD脑中的分子畸变反映在脑脊液(CSF)中,最近已鉴定出三种候选生物标志物:总tau蛋白,淀粉样蛋白β-1-42和在AD特异性表位磷酸化的tau蛋白。这些数据的敏感性和特异性能够区分AD患者与对照。在这里,我们回顾了有关生化生物标记物的最新文献,并讨论了它们的预测价值,可作为疾病易感性的指标,以检测具有AD风险的个体并确定新颖的疾病缓解策略的临床疗效。根据本综述中报道的文献分析,我们可以得出结论,脑脊液生物标志物及其比率的组合可能会显着提高AD诊断的特异性和准确性。

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