Department of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu, No. 37, Guo Xue Xiang, Chengdu 610041, The People's Republic of China.
Int Immunol. 2010 Jul;22(7):611-8. doi: 10.1093/intimm/dxq043. Epub 2010 May 24.
To identify novel serum protein biomarkers and establish diagnostic pattern for rheumatoid arthritis (RA) by using proteomic technology.
Serum proteomic spectra were generated by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) combined with weak cationic exchange magnetic beads. A training set of spectra, derived from analyzing sera from 22 patients with RA, 26 patients with other autoimmune diseases and 25 age- and sex-matched healthy volunteers, was used to train and develop a decision tree model with a machine learning algorithm called decision boosting. A blinded testing set, including 21 patients with RA, 24 patients with other autoimmune diseases and 25 healthy people, was used to examine the accuracy of the model.
A decision tree model was established, consisting of four potential protein biomarkers whose m/z values were 4966.88, 5065.3, 5636.97 and 7766.87, respectively. In validation test, the decision tree model could differentiate RA from other autoimmune diseases and healthy people with the sensitivity of 85.71% and specificity of 87.76%, respectively.
The present data suggested that MALDI-TOF-MS combined with magnetic beads could screen and identify some novel serum protein biomarkers related to RA. The proteomic pattern based on the four candidate biomarkers is of value for laboratory diagnosis of RA.
利用蛋白质组学技术鉴定新的血清蛋白生物标志物并建立类风湿关节炎(RA)的诊断模式。
采用基质辅助激光解吸电离飞行时间质谱(MALDI-TOF-MS)联合弱阳离子交换磁珠技术生成血清蛋白质组谱。利用从 22 例 RA 患者、26 例其他自身免疫性疾病患者和 25 名年龄和性别匹配的健康志愿者的血清中分析得出的训练集光谱,采用一种称为决策提升的机器学习算法来训练和开发决策树模型。一个包括 21 例 RA 患者、24 例其他自身免疫性疾病患者和 25 名健康人的盲法测试集用于检验该模型的准确性。
建立了一个决策树模型,由四个潜在的蛋白生物标志物组成,其 m/z 值分别为 4966.88、5065.3、5636.97 和 7766.87。在验证性试验中,该决策树模型可以将 RA 与其他自身免疫性疾病和健康人区分开来,其敏感性分别为 85.71%和特异性为 87.76%。
本研究数据表明,MALDI-TOF-MS 联合磁珠可筛选和鉴定出一些与 RA 相关的新型血清蛋白生物标志物。基于这四个候选生物标志物的蛋白质组模式对 RA 的实验室诊断具有一定的价值。