Department of Biochemistry, Institute of Biomedicine and Translational Medicine, University of Tartu, Ravila 14b, 50411, Tartu, Estonia.
Centre of Excellence for Genomics and Translational Medicine, University of Tartu, Tartu, Estonia.
Arch Dermatol Res. 2017 Sep;309(7):519-528. doi: 10.1007/s00403-017-1760-1. Epub 2017 Jul 10.
The majority of studies on psoriasis have focused on explaining the genetic background and its associations with the immune system's response. The aim of this study was to identify the low-molecular weight compounds contributing to the metabolomic profile of psoriasis and to provide computational models that help with the classification and monitoring of the severity of the disease. We compared the results from targeted and untargeted analyses of patients' serums with plaque psoriasis to controls. The main differences were found in the concentrations of acylcarnitines, phosphatidylcholines, amino acids, urea, phytol, and 1,11-undecanedicarboxylic acid. The data from the targeted analysis were used to build classification models for psoriasis. The results from this study provide an overview of the metabolomic serum profile of psoriasis along with promising statistical models for the monitoring of the disease.
大多数关于银屑病的研究都集中在解释其遗传背景及其与免疫系统反应的关联。本研究旨在确定导致银屑病代谢组学特征的低分子量化合物,并提供有助于疾病分类和严重程度监测的计算模型。我们将斑块状银屑病患者的血清进行靶向和非靶向分析的结果与对照组进行了比较。主要差异存在于酰基辅酶 A、磷脂酰胆碱、氨基酸、尿素、植醇和 1,11-十一烷二酸的浓度中。靶向分析的数据被用于构建银屑病的分类模型。本研究提供了银屑病代谢组学血清特征的概述,以及用于监测疾病的有前途的统计模型。