肌无力和多发性硬化症患者血清氨基酸谱的比较分析

Piotr Kośliński, Łukasz Rzepiński, M. Koba, Zdzisław Maciejek, Mariusz Kowalewski, Emilia Daghir-Wojtkowiak
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摘要

背景:多发性硬化症(MS)和重症肌无力(MG)是分别侵犯中枢神经系统(CNS)和神经肌肉接头的自身免疫性疾病。由于这两种疾病的共同发病机制都与自身免疫背景以及 T 淋巴细胞和 B 淋巴细胞的参与有关,某些临床症状的重叠可能会给这两种疾病的鉴别诊断带来困难。研究方法本研究旨在使用液相色谱-电喷雾离子化-质谱联用仪(LC-ESI-MS/MS),结合多变量统计分析,研究多发性硬化症患者、多发性硬化症患者和对照组之间氨基酸代谢谱的变化。结果通过对多发性硬化症患者、多发性硬化症患者和对照组之间的氨基酸(AA)进行比较分析,可以发现氨基酸谱存在显著的统计学差异。将患者(多发性硬化症和多发性硬化症患者)与对照组进行比较,并将多重测试结果考虑在内后,发现各组之间的氨基酸(如 ARG、PRO、TRP、CIT)存在明显差异。在比较多发性硬化症患者和多发性硬化症患者的 AA 浓度时,我们发现多发性硬化症组和多发性硬化症组中有三种 AA(CIT、GABA 和 AAA)在多重测试校正后存在显著差异。在重症肌无力患者中观察到的氨基酸浓度较高,且存在显著差异。结论:我们的研究结果表明,氨基酸对改善 MS 和 MG 患者的诊断很有价值。为了更好地评估这些标记物的潜在作用,需要在更大的研究群体中进一步验证它们的性能,并限制可能的混杂因素,如药物和饮食。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative Analysis of Serum Amino Acid Profiles in Patients with Myasthenia Gravis and Multiple Sclerosis
Background: Multiple sclerosis (MS) and myasthenia gravis (MG) are autoimmune diseases that attack the central nervous system (CNS) and the neuromuscular junction, respectively. As the common pathogenesis of both diseases is associated with an autoimmune background and the involvement of T and B lymphocytes, the overlapping of selected clinical symptoms may cause difficulties in the differential diagnosis of both diseases. Methods: The aim of the study was to use Liquid Chromatography–Electrospray Ionization–Mass Spectrometry (LC–ESI–MS/MS) in conjunction with multivariate statistical analyses to examine the changes in amino acid metabolic profiles between patients with MG, MS, and a control group. Results: Comparative analysis of amino acids (AA) between patients with MG, MS, and within the control group allowed for the identification of statistically significant differences in the amino acid profile. Comparing the patients (patients with MS and MG) with the control group, and after taking the results of multiple tests into account, it was observed that amino acids such as ARG, PRO, TRP, CIT were significantly different between the groups. When considering the comparison between the AA concentrations in MS and MG patients, we found three AAs that were significantly different in the MS and MG groups, after correcting for multiple testing (CIT, GABA, and AAA). Higher concentrations of amino acids that showed significant differences were observed in patients with myasthenia gravis. Conclusions: Our results have indicated AAs that may prove valuable for improving the diagnostics of MS and MG patients. To better assess the potential utility of these markers, their performance requires further validation in a larger study group and limitation of possible confounding factors, e.g., medications and diet.
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