Department of Neurosurgery, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, Aichi 466-8550, Japan.
BMC Neurol. 2010 Nov 8;10:112. doi: 10.1186/1471-2377-10-112.
Moyamoya disease (MMD) is an uncommon cerebrovascular condition with unknown etiology characterized by slowly progressive stenosis or occlusion of the bilateral internal carotid arteries associated with an abnormal vascular network. MMD is a major cause of stroke, specifically in the younger population. Diagnosis is based on only radiological features as no other clinical data are available. The purpose of this study was to identify novel biomarker candidate proteins differentially expressed in the cerebrospinal fluid (CSF) of patients with MMD using proteomic analysis.
For detection of biomarkers, CSF samples were obtained from 20 patients with MMD and 12 control patients. Mass spectral data were generated by surface-enhanced laser desorption/ionization time-of-flight mass spectrometry (SELDI-TOF-MS) with an anion exchange chip in three different buffer conditions. After expression difference mapping was undertaken using the obtained protein profiles, a comparative analysis was performed.
A statistically significant number of proteins (34) were recognized as single biomarker candidate proteins which were differentially detected in the CSF of patients with MMD, compared to the control patients (p < 0.05). All peak intensity profiles of the biomarker candidates underwent classification and regression tree (CART) analysis to produce prediction models. Two important biomarkers could successfully classify the patients with MMD and control patients.
In this study, several novel biomarker candidate proteins differentially expressed in the CSF of patients with MMD were identified by a recently developed proteomic approach. This is a pilot study of CSF proteomics for MMD using SELDI technology. These biomarker candidates have the potential to shed light on the underlying pathogenesis of MMD.
烟雾病(MMD)是一种病因不明的罕见脑血管病,其特征为双侧颈内动脉逐渐狭窄或闭塞,伴异常血管网形成。MMD 是脑卒中的主要病因,尤其是在年轻人群中。目前仅依据影像学特征进行诊断,尚无其他临床数据。本研究旨在采用蛋白质组学分析方法,鉴定 MMD 患者脑脊液中差异表达的新型候选生物标志物蛋白。
为了检测生物标志物,收集了 20 例 MMD 患者和 12 例对照患者的脑脊液样本。采用表面增强激光解吸电离飞行时间质谱(SELDI-TOF-MS)技术,在三种不同缓冲条件下利用阴离子交换芯片产生质谱数据。通过获得的蛋白质图谱进行表达差异映射后,进行比较分析。
与对照组相比,MMD 患者脑脊液中差异检测到 34 种具有统计学意义的蛋白(p<0.05),被认为是单一候选生物标志物蛋白。对所有候选生物标志物的峰强度图谱进行分类和回归树(CART)分析,以生成预测模型。两种重要的生物标志物可成功区分 MMD 患者和对照组。
本研究采用一种新的蛋白质组学方法,鉴定了 MMD 患者脑脊液中差异表达的多种新型候选生物标志物蛋白。这是一项采用 SELDI 技术的 MMD 脑脊液蛋白质组学的初步研究。这些候选生物标志物有可能揭示 MMD 的潜在发病机制。