Židó Michal, Kačer David, Valeš Karel, Svobodová Zuzana, Zimová Denisa, Štětkárová Ivana
Department of Neurology, Third Faculty of Medicine, Charles University, Prague, Czechia.
Department of Neurology, Faculty Hospital Královské Vinohrady, Prague, Czechia.
Front Neurol. 2022 May 26;13:874121. doi: 10.3389/fneur.2022.874121. eCollection 2022.
Multiple sclerosis (MS) is a chronic autoimmune disease of the central nervous system (CNS) leading to the loss of myelin and axons. Diagnosis is based on clinical findings, MRI, and analysis of cerebrospinal fluid (CSF). CSF is an ultrafiltrate of plasma and reflects inflammatory processes in the CNS. The aim of this study was to perform metabolomics analysis of CSF in patients after the first attack of MS and healthy controls and try to find new specific analytes for MS including those potentially predicting disease activities at the onset.
We collected CSF from 19 patients (16 females, aged 19-55 years) after the first attack of clinical symptoms who fulfilled revised McDonald criteria of MS and CSF of 19 controls (16 females, aged 19-50 years). Analyses of CSF samples were provided using the high-performance liquid chromatography system coupled with a mass spectrometer with a high-resolution detector (TripleTOF 5600, AB Sciex, Canada).
Approximately 130 selected analytes were identified, and 30 of them were verified. During the targeted analysis, a significant decrease in arginine and histidine and a less significant decrease in the levels of asparagine, leucine/isoleucine, and tryptophan, together with a significant increase of palmitic acid in the patient group, were found.
We observed significant differences in amino and fatty acids in the CSF of newly diagnosed patients with MS in comparison with controls. The most significant changes were observed in levels of arginine, histidine, and palmitic acid that may predict inflammatory disease activity. Further studies are necessary to support these findings as potential biomarkers of MS.
多发性硬化症(MS)是一种中枢神经系统(CNS)的慢性自身免疫性疾病,会导致髓鞘和轴突的丧失。诊断基于临床症状、磁共振成像(MRI)以及脑脊液(CSF)分析。脑脊液是血浆的超滤液,反映中枢神经系统的炎症过程。本研究的目的是对首次发作后多发性硬化症患者的脑脊液进行代谢组学分析,并与健康对照进行比较,试图找到新的多发性硬化症特异性分析物,包括那些可能在发病时预测疾病活动的分析物。
我们收集了19例符合修订的麦克唐纳多发性硬化症标准且首次出现临床症状发作后的患者(16名女性,年龄19 - 55岁)的脑脊液,以及19名对照者(16名女性,年龄19 - 50岁)的脑脊液。使用配备高分辨率检测器的液相色谱系统与质谱仪(TripleTOF 5600,AB Sciex,加拿大)对脑脊液样本进行分析。
共鉴定出约130种选定的分析物,其中30种得到验证。在靶向分析中,发现患者组中精氨酸和组氨酸显著降低,天冬酰胺、亮氨酸/异亮氨酸和色氨酸水平降低程度较小,同时棕榈酸显著增加。
我们观察到新诊断的多发性硬化症患者脑脊液中的氨基酸和脂肪酸与对照组相比存在显著差异。在精氨酸、组氨酸和棕榈酸水平上观察到的变化最为显著,这些变化可能预测炎症性疾病活动。需要进一步研究以支持这些发现作为多发性硬化症的潜在生物标志物。