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Fusion of metabolomics and proteomics data for biomarkers discovery: case study on the experimental autoimmune encephalomyelitis

机译:融合代谢组学和蛋白质组学数据以发现生物标志物:实验性自身免疫性脑脊髓炎的案例研究

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Background Analysis of Cerebrospinal Fluid (CSF) samples holds great promise to diagnose neurological pathologies and gain insight into the molecular background of these pathologies. Proteomics and metabolomics methods provide invaluable information on the biomolecular content of CSF and thereby on the possible status of the central nervous system, including neurological pathologies. The combined information provides a more complete description of CSF content. Extracting the full combined information requires a combined analysis of different datasets i.e. fusion of the data. Results A novel fusion method is presented and applied to proteomics and metabolomics data from a pre-clinical model of multiple sclerosis: an Experimental Autoimmune Encephalomyelitis (EAE) model in rats. The method follows a mid-level fusion architecture. The relevant information is extracted per platform using extended canonical variates analysis. The results are subsequently merged in order to be analyzed jointly. We find that the combined proteome and metabolome data allow for the efficient and reliable discrimination between healthy, peripherally inflamed rats, and rats at the onset of the EAE. The predicted accuracy reaches 89% on a test set. The important variables (metabolites and proteins) in this model are known to be linked to EAE and/or multiple sclerosis. Conclusions Fusion of proteomics and metabolomics data is possible. The main issues of high-dimensionality and missing values are overcome. The outcome leads to higher accuracy in prediction and more exhaustive description of the disease profile. The biological interpretation of the involved variables validates our fusion approach.
机译:脑脊液(CSF)样品的背景分析对诊断神经病理学和深入了解这些病理学的分子背景具有广阔的前景。蛋白质组学和代谢组学方法可提供有关CSF生物分子含量的宝贵信息,从而可提供有关中枢神经系统可能状态(包括神经病理学)的宝贵信息。组合的信息提供了对CSF内容的更完整描述。提取完整的组合信息需要对不同数据集进行组合分析,即数据融合。结果提出了一种新颖的融合方法,并将其应用于多发性硬化的临床前模型:大鼠实验性自身免疫性脑脊髓炎(EAE)模型的蛋白质组学和代谢组学数据。该方法遵循中级融合架构。使用扩展的规范变量分析按平台提取相关信息。随后将结果合并以便一起分析。我们发现,结合蛋白质组和代谢组学数据可以对健康,周围发炎的大鼠和EAE发作的大鼠进行有效而可靠的区分。在测试集上,预测精度达到89%。已知该模型中的重要变量(代谢产物和蛋白质)与EAE和/或多发性硬化症有关。结论蛋白质组学和代谢组学数据的融合是可能的。高维和缺失值的主要问题已得到克服。结果导致更高的预测准确性和更详尽的疾病描述。对涉及变量的生物学解释证实了我们的融合方法。

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