The Peripheral Profile of the Chitinase 3-like-1 in Benign Multiple Sclerosis - A Single Centre's Experience.

IF 2.7 4区 医学 Q3 NEUROSCIENCES
Laura Barcutean, Adina Hutanu, Sebastian Andone, Smaranda Maier, Rodica Balasa
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引用次数: 0

Abstract

Background: A limited subgroup of multiple sclerosis (MS) patients present with a longterm disease evolution characterized by a limited disease progression, known as benign MS (BMS). Chitinase 3-like-1 (CHI3L1) levels are sensitive to inflammatory processes and may play a role in the pathogenesis of MS. In this observational, cross-sectional study, we aimed to evaluate the implications of serum CHI3L1 and inflammatory cytokines in BMS patients treated with interferon β-1b for over a decade.

Methods: We collected serum samples from 17 BMS patients and 17 healthy controls (HC) to measure serum CHI3L1 levels and a Th17 panel of inflammatory cytokines. Serum levels of CHI3L1 were analysed using the sandwich ELISA method and the Th17 panel was assessed using the multiplex XMap technology on a Flexmap 3D Analyzer.

Results: Serum CHI3L1 levels did not differ significantly from HC. We identified a positive correlation between CHI3L1 levels and relapses during treatment.

Conclusion: Our findings suggest that there are no differences in serum CHI3L1 levels between BMS patients and HC. However, serum CHI3L1 levels are sensitive to clinical inflammatory activity and may be associated with relapses in BMS patients.

几丁质酶 3-like-1 在良性多发性硬化症中的外周特征--一个单一中心的经验。
背景:在多发性硬化症(MS)患者中,有一个有限的亚群表现为长期的疾病演变,其特点是疾病进展有限,被称为良性多发性硬化症(BMS)。几丁质酶 3-like-1 (CHI3L1) 的水平对炎症过程很敏感,可能在多发性硬化症的发病机制中发挥作用。在这项观察性横断面研究中,我们旨在评估十多年来接受干扰素β-1b治疗的BMS患者血清CHI3L1和炎症细胞因子的影响:我们采集了17名BMS患者和17名健康对照者(HC)的血清样本,测量血清CHI3L1水平和Th17炎症细胞因子。使用夹心酶联免疫吸附法分析血清中的 CHI3L1 水平,并使用 Flexmap 3D 分析仪上的多重 XMap 技术评估 Th17 面板:结果:血清CHI3L1水平与HC无明显差异。我们发现 CHI3L1 水平与治疗期间的复发率呈正相关:我们的研究结果表明,BMS 患者和 HC 患者的血清 CHI3L1 水平没有差异。然而,血清 CHI3L1 水平对临床炎症活动很敏感,可能与 BMS 患者的复发有关。
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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来源期刊
CiteScore
5.10
自引率
3.30%
发文量
158
审稿时长
6-12 weeks
期刊介绍: Aims & Scope CNS & Neurological Disorders - Drug Targets aims to cover all the latest and outstanding developments on the medicinal chemistry, pharmacology, molecular biology, genomics and biochemistry of contemporary molecular targets involved in neurological and central nervous system (CNS) disorders e.g. disease specific proteins, receptors, enzymes, genes. CNS & Neurological Disorders - Drug Targets publishes guest edited thematic issues written by leaders in the field covering a range of current topics of CNS & neurological drug targets. The journal also accepts for publication original research articles, letters, reviews and drug clinical trial studies. As the discovery, identification, characterization and validation of novel human drug targets for neurological and CNS drug discovery continues to grow; this journal is essential reading for all pharmaceutical scientists involved in drug discovery and development.
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