de Seny Dominique, Fillet Marianne, Meuwis Marie-Alice, Geurts Pierre, Lutteri Laurence, Ribbens Clio, Bours Vincent, Wehenkel Louis, Piette Jacques, Malaise Michel, Merville Marie-Paule
University of Liège, Centre Hospitalier Universitaire, Liege, Belgium.
Arthritis Rheum. 2005 Dec;52(12):3801-12. doi: 10.1002/art.21607.
To identify serum protein biomarkers specific for rheumatoid arthritis (RA), using surface-enhanced laser desorption/ionization time-of-flight mass spectrometry (SELDI-TOF-MS) technology.
A total of 103 serum samples from patients and healthy controls were analyzed. Thirty-four of the patients had a diagnosis of RA, based on the American College of Rheumatology criteria. The inflammation control group comprised 20 patients with psoriatic arthritis (PsA), 9 with asthma, and 10 with Crohn's disease. The noninflammation control group comprised 14 patients with knee osteoarthritis and 16 healthy control subjects. Serum protein profiles were obtained by SELDI-TOF-MS and compared in order to identify new biomarkers specific for RA. Data were analyzed by a machine learning algorithm called decision tree boosting, according to different preprocessing steps.
The most discriminative mass/charge (m/z) values serving as potential biomarkers for RA were identified on arrays for both patients with RA versus controls and patients with RA versus patients with PsA. From among several candidates, the following peaks were highlighted: m/z values of 2,924 (RA versus controls on H4 arrays), 10,832 and 11,632 (RA versus controls on CM10 arrays), 4,824 (RA versus PsA on H4 arrays), and 4,666 (RA versus PsA on CM10 arrays). Positive results of proteomic analysis were associated with positive results of the anti-cyclic citrullinated peptide test. Our observations suggested that the 10,832 peak could represent myeloid-related protein 8.
SELDI-TOF-MS technology allows rapid analysis of many serum samples, and use of decision tree boosting analysis as the main statistical method allowed us to propose a pattern of protein peaks specific for RA.
采用表面增强激光解吸/电离飞行时间质谱(SELDI-TOF-MS)技术鉴定类风湿关节炎(RA)特异性血清蛋白生物标志物。
共分析了103例患者和健康对照者的血清样本。根据美国风湿病学会标准,其中34例患者被诊断为RA。炎症对照组包括20例银屑病关节炎(PsA)患者、9例哮喘患者和10例克罗恩病患者。非炎症对照组包括14例膝骨关节炎患者和16例健康对照者。通过SELDI-TOF-MS获得血清蛋白谱并进行比较,以鉴定RA特异性新生物标志物。根据不同的预处理步骤,采用一种名为决策树增强的机器学习算法对数据进行分析。
在RA患者与对照组以及RA患者与PsA患者的阵列上均鉴定出了作为RA潜在生物标志物的最具鉴别力的质荷比(m/z)值。在几个候选物中,突出显示了以下峰:2924的m/z值(H4阵列上RA与对照组)、10832和11632(CM10阵列上RA与对照组)、4824(H4阵列上RA与PsA)以及4666(CM10阵列上RA与PsA)。蛋白质组学分析的阳性结果与抗环瓜氨酸肽试验的阳性结果相关。我们的观察结果表明,10832峰可能代表髓样相关蛋白8。
SELDI-TOF-MS技术可快速分析许多血清样本,将决策树增强分析作为主要统计方法使我们能够提出一种RA特异性的蛋白峰模式。