Metabolomics Core Laboratory, Healthy Aging Research Center, Chang Gung University, Taoyuan, Taiwan.
Department of Medical Biotechnology and Laboratory Science, College of Medicine, Chang Gung University, Taoyuan, Taiwan.
Sci Rep. 2017 Aug 15;7(1):8140. doi: 10.1038/s41598-017-08338-7.
Guillain-Barre Syndrome (GBS) is an inflammatory disease of the peripheral nervous system. Given that plasma metabolic profiles in GBS patients have never been explored, plasma samples of 38 GBS patients, 22 multiple sclerosis (MS) patients, and 40 healthy controls were analyzed by using untargeted and targeted metabolomics analysis. The untargeted analysis showed that levels of a set of plasma lipid metabolites were significantly decreased in GBS patients compared to the controls. Furthermore, the targeted analysis demonstrated that levels of 41 metabolites in GBS patients were significantly changed compared to either the controls or MS patients. A further metabolic analysis showed that 12 of 41 metabolites were significantly lower in classical GBS patients compared to Miller-Fisher syndrome. Among them, each of PCae C34:0, PCae C42:2, PCae C42:3, and SM C24:0 was inversely correlated with Hughes functional grading scale of GBS patients at both nadir and discharge. Receiver operating characteristic curve analysis of combination of three metabolites (PCaa C42:2, PCae C36:0 and SM C24:0) showed a good discrimination between the GBS and the controls (area under curve = 0.86). This study has demonstrated disruption of lipid metabolites in GBS may be potential biomarkers to indicate disease severity and prognosis of GBS.
格林-巴利综合征(GBS)是一种周围神经系统的炎症性疾病。鉴于 GBS 患者的血浆代谢谱从未被探索过,我们对 38 名 GBS 患者、22 名多发性硬化症(MS)患者和 40 名健康对照者的血浆样本进行了非靶向和靶向代谢组学分析。非靶向分析表明,与对照组相比,GBS 患者的一组血浆脂质代谢物水平显著降低。此外,靶向分析表明,与对照组或 MS 患者相比,GBS 患者中有 41 种代谢物的水平发生了显著变化。进一步的代谢分析表明,与米勒-费舍尔综合征相比,经典 GBS 患者中有 12 种代谢物显著降低。其中,每个 PCae C34:0、PCae C42:2、PCae C42:3 和 SM C24:0 均与 GBS 患者的休斯功能分级量表在最低点和出院时呈负相关。三种代谢物(PCaa C42:2、PCae C36:0 和 SM C24:0)组合的受试者工作特征曲线分析显示,它们可以很好地区分 GBS 和对照组(曲线下面积 = 0.86)。本研究表明,GBS 中脂质代谢物的破坏可能是指示疾病严重程度和 GBS 预后的潜在生物标志物。