Department of Clinical Epidemiology, Ningbo No. 2 Hospital, Ningbo, Zhejiang 315000, China.
Center for Cardiovascular and Cerebrovascular Epidemiology and Translational Medicine, Guoke Ningbo Life Science and Health Industry Research Institute, University of Chinese Academy of Sciences, Ningbo, Zhejiang 315000, China.
J Proteome Res. 2024 Sep 6;23(9):4082-4094. doi: 10.1021/acs.jproteome.4c00394. Epub 2024 Aug 21.
We aimed to uncover the pathological mechanism of ischemic stroke (IS) using a combined analysis of untargeted metabolomics and proteomics. The serum samples from a discovery set of 44 IS patients and 44 matched controls were analyzed using a specific detection method. The same method was then used to validate metabolites and proteins in the two validation sets: one with 30 IS patients and 30 matched controls, and the other with 50 IS patients and 50 matched controls. A total of 105 and 221 differentially expressed metabolites or proteins were identified, and the association between the two omics was determined in the discovery set. Enrichment analysis of the top 25 metabolites and 25 proteins in the two-way orthogonal partial least-squares with discriminant analysis, which was employed to identify highly correlated biomarkers, highlighted 15 pathways relevant to the pathological process. One metabolite and seven proteins exhibited differences between groups in the validation set. The binary logistic regression model, which included metabolite 2-hydroxyhippuric acid and proteins APOM_O95445, MASP2_O00187, and PRTN3_D6CHE9, achieved an area under the curve of 0.985 (95% CI: 0.966-1) in the discovery set. This study elucidated alterations and potential coregulatory influences of metabolites and proteins in the blood of IS patients.
我们旨在通过非靶向代谢组学和蛋白质组学的联合分析来揭示缺血性脑卒中(IS)的病理机制。使用特定的检测方法对来自 44 名 IS 患者和 44 名匹配对照的发现集的血清样本进行分析。然后,使用相同的方法验证两个验证集中的代谢物和蛋白质:一个有 30 名 IS 患者和 30 名匹配对照,另一个有 50 名 IS 患者和 50 名匹配对照。在发现集中确定了 105 个和 221 个差异表达的代谢物或蛋白质,并确定了两种组学之间的关联。双向正交偏最小二乘判别分析的前 25 个代谢物和 25 个蛋白质的富集分析,用于识别高度相关的生物标志物,突出了与病理过程相关的 15 条途径。在验证集中,一个代谢物和七个蛋白质在组间存在差异。包括代谢物 2-羟基苯乙酸和蛋白质 APOM_O95445、MASP2_O00187 和 PRTN3_D6CHE9 的二元逻辑回归模型在发现集中的曲线下面积为 0.985(95%CI:0.966-1)。本研究阐明了 IS 患者血液中代谢物和蛋白质的变化及其潜在的核心调节影响。