Marksteiner Josef, Hinterhuber Hartmann, Humpel Christian
Department of General Psychiatry, Innsbruck Medical University, Innsbruck, Austria.
Drugs Today (Barc). 2007 Jun;43(6):423-31. doi: 10.1358/dot.2007.43.6.1067341.
Alzheimer's disease is a chronic progressive neurodegenerative disease and it is the most prevalent type of dementia. Diagnostic means, including neuroimaging methods, are continuously improving. Nevertheless, it is still a challenge to increase the sensitivity and specificity of a diagnosis of Alzheimer's disease. Two diagnostic areas are especially challenging: first, differentiating early stages of Alzheimer's disease from mild cognitive impairment and normal aging; and second, increasing diagnostic specificity especially when similar clinical symptoms are shared by various types of dementia. To date, the analysis of beta-amyloid(1-42), total tau and phospho-tau-181 from cerebrospinal fluid (CSF) are the best biological markers to diagnose Alzheimer's disease and differentiate it from other forms of dementia with a high reliability and validity. This article reviews the use of CSF biomarkers and of putative blood-related markers.
阿尔茨海默病是一种慢性进行性神经退行性疾病,也是最常见的痴呆类型。包括神经影像学方法在内的诊断手段在不断改进。然而,提高阿尔茨海默病诊断的敏感性和特异性仍然是一项挑战。有两个诊断领域尤其具有挑战性:第一,将阿尔茨海默病的早期阶段与轻度认知障碍和正常衰老区分开来;第二,提高诊断特异性,尤其是当各种类型的痴呆症都有相似的临床症状时。迄今为止,对脑脊液(CSF)中的β-淀粉样蛋白(1-42)、总tau蛋白和磷酸化tau-181进行分析是诊断阿尔茨海默病并将其与其他形式的痴呆症区分开来的最佳生物学标志物,具有较高的可靠性和有效性。本文综述了脑脊液生物标志物和假定的血液相关标志物的应用。