Simonsen A H, Hagnelius N-O, Waldemar G, Nilsson T K, McGuire J
Memory Disorders Research Group Section 6702, Department of Neurology, Copenhagen University Hospital Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen, Denmark.
Int J Proteomics. 2012;2012:824024. doi: 10.1155/2012/824024. Epub 2012 Jun 4.
Alzheimer's disease (AD) is the most common form of dementia found in all human populations worldwide, while vascular dementia (VaD) is the second most common form of dementia. New biomarkers for early and specific diagnosis of AD and VaD are needed to achieve greater insight into changes occurring in the brain and direct therapeutic strategies. The objective of this explorative study was to discover candidate protein biomarkers for the differential diagnosis between VaD and AD. Surface-enhanced laser desorption/ionization (SELDI) TOF-MS was used to differentially profile proteins and peptides in CSF samples from 28 AD patients and 21 patients with VaD. A combination of univariate (Kruskal-Wallis) and multivariate (independent component analysis) statistical approaches produced a list of 27 proteins and peptides that could differentiate between VaD and AD. These markers represent various physiological processes, such as protein degradation (ubiquitin), protease inhibition (cystatin C and alpha-1-antichymoptrypsin), and inflammation (C3a and C4a) that are known to be represented in neurodegenerative diseases.
阿尔茨海默病(AD)是全球所有人群中最常见的痴呆形式,而血管性痴呆(VaD)是第二常见的痴呆形式。需要新的生物标志物来早期、特异性诊断AD和VaD,以便更深入了解大脑中发生的变化并指导治疗策略。这项探索性研究的目的是发现用于VaD和AD鉴别诊断的候选蛋白质生物标志物。表面增强激光解吸/电离(SELDI)飞行时间质谱(TOF-MS)用于对28例AD患者和21例VaD患者的脑脊液样本中的蛋白质和肽进行差异分析。单变量(Kruskal-Wallis)和多变量(独立成分分析)统计方法相结合,得出了一份可区分VaD和AD的27种蛋白质和肽的列表。这些标志物代表了各种生理过程,如蛋白质降解(泛素)、蛋白酶抑制(胱抑素C和α-1抗糜蛋白酶)以及炎症(C3a和C4a),这些在神经退行性疾病中都有体现。