Assessment of Serum Uric Acid Levels in Multiple Sclerosis during Disease-Modifying Treatment

A. Podlecka-Piętowska, Joanna Przybek, Kamil Chorążka, M. Nojszewska, B. Zakrzewska-Pniewska, A. Kaminska
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引用次数: 1

Abstract

Objective: Uric acid is a potent endogenous antioxidant and scavenger of peroxynitrite (PN), which hypothesized to be involved in the pathogenesis of multiple sclerosis (MS). Some studies reported lower levels of UA in MS patients compared with controls, whereas other studies found no difference. The main purpose of this analysis was to verify the hypothesis on lower serum levels of UA in MS patients compared with controls.Materials and methods: We examined 80 patients with clinically defined MS, according to the McDonald’s criteria and 53 patients of controls group (non-inflammatory neurological diseases, excluding vascular disorders). Uric acid concentration was determined by using a commercially available enzymatic colorimetric assay according to the manufacturer’s instructions.Results: Serum UA levels of MS patients were significantly lower (4.2 ± 1.1 mg/dl) when compared with control group (4.9 ± 1.4 mg/dl, P=0.0092). Correlation between MS duration and serum UA concentration did not reach statistical significance, however the tendency showing that patients who are suffering from this disorder for a longer time have lower serum UA concentration was observed. Moreover, we found a statistically significant correlation between disease duration and UA concentration in a subgroup of patient who did not have a history of mitoxantrone intake (P<0.0321).Conclusion: Although we do not know exactly whether and how uric acid is involved in MS pathogenesis, data suggest that UA concentration is lower in MS patients than in control group. It seems that low uric acid levels indicate patients with a higher risk of disease progression. Whether or not UA concentration can be useful as a biomarker in MS requires further study.
多发性硬化症治疗期间血清尿酸水平的评估
目的:尿酸是一种有效的内源性抗氧化剂和过氧亚硝酸盐(PN)的清除剂,它被认为参与了多发性硬化症(MS)的发病机制。一些研究报告称,与对照组相比,MS患者的UA水平较低,而其他研究则没有发现差异。本分析的主要目的是验证MS患者与对照组相比血清UA水平较低的假设。材料和方法:我们检查了80例临床定义为MS的患者,根据麦当劳标准和53例对照组(非炎症性神经系统疾病,不包括血管疾病)。尿酸浓度测定采用市售酶比色法根据制造商的说明。结果:MS患者血清UA水平(4.2±1.1 mg/dl)明显低于对照组(4.9±1.4 mg/dl, P=0.0092)。MS病程与血清UA浓度的相关性无统计学意义,但患者病程越长,血清UA浓度越低。此外,我们发现在没有米托蒽醌摄入史的患者亚组中,病程与UA浓度之间存在统计学意义上的相关性(P<0.0321)。结论:虽然我们不清楚尿酸是否以及如何参与MS的发病过程,但资料显示MS患者UA浓度低于对照组。似乎低尿酸水平表明患者疾病进展的风险更高。UA浓度是否可以作为MS的生物标志物还有待进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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