Simonsen Anja H, McGuire James, Hansson Oskar, Zetterberg Henrik, Podust Vladimir N, Davies Huw A, Waldemar Gunhild, Minthon Lennart, Blennow Kaj
Biomarker Discovery Center Facility, Ciphergen Biosystems, Inc., 2100 Copenhagen O, Denmark.
Arch Neurol. 2007 Mar;64(3):366-70. doi: 10.1001/archneur.64.3.366.
To use proteomic analysis of cerebrospinal fluid to discover novel proteins and peptides able to differentiate between patients with stable mild cognitive impairment (MCI) and those who will progress to Alzheimer disease (AD).
Baseline cerebrospinal fluid samples from patients with MCI and healthy controls were profiled using surface-enhanced laser desorption/ionization time-of-flight mass spectrometry.
Memory disorder clinic.
Patients with MCI (n = 113), of whom 56 were cognitively stable and 57 progressed to AD with dementia during a 4- to 6-year follow-up, as well as 28 healthy controls who were followed up for 3 years. Main Outcome Measure During follow-up, 57 patients progressed to AD and 56 patients had stable MCI. Cerebrospinal fluid from these 2 groups of patients was compared using surface-enhanced laser desorption/ionization time-of-flight mass spectrometry.
We identified a panel of 17 potential biomarkers that could distinguish between patients with stable MCI and patients with MCI who progressed to AD. We have positively identified and characterized 5 of the potential biomarkers.
Proteomic profiling of cerebrospinal fluid provided a novel panel of 17 potential biomarkers for prediction of MCI progression to AD. The 5 identified biomarkers are relevant to the pathogenesis of AD and could help gain an understanding of the molecular pathways in which they may function.
运用脑脊液蛋白质组学分析来发现能够区分稳定型轻度认知障碍(MCI)患者和将进展为阿尔茨海默病(AD)患者的新型蛋白质和肽段。
采用表面增强激光解吸/电离飞行时间质谱法对MCI患者和健康对照者的基线脑脊液样本进行分析。
记忆障碍诊所。
MCI患者(n = 113),其中56例认知功能稳定,57例在4至6年的随访期间进展为伴有痴呆的AD,以及28名健康对照者,随访3年。主要观察指标在随访期间,57例患者进展为AD,56例患者MCI稳定。使用表面增强激光解吸/电离飞行时间质谱法比较这两组患者的脑脊液。
我们鉴定出一组17种潜在生物标志物,可区分稳定型MCI患者和进展为AD的MCI患者。我们已对其中5种潜在生物标志物进行了阳性鉴定和表征。
脑脊液蛋白质组学分析提供了一组17种潜在生物标志物,用于预测MCI进展为AD。已鉴定出的5种生物标志物与AD的发病机制相关,有助于了解它们可能发挥作用的分子途径。