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Less Frequent and Less Severe Flu-Like Syndrome in Interferon Beta-1a Treated Multiple Sclerosis Patients with at Least One Allele Bearing the GC Polymorphism at Position -174 of the IL-6 Promoter Gene

机译:干扰素β-1a治疗的多发性硬化症患者中出现频率最低且重度较低的多发性硬化症患者其中至少一个等位基因在IL-6启动子基因的-174位具有G C多态性

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摘要

One of the most common adverse event of interferon beta (IFNβ) therapy for multiple sclerosis is flu-like syndrome (FLS), which has been reportedly related to increased levels of cytokines such as interleukin 6 (IL-6) and tumor necrosis factor-alpha (TNF-α). Average cytokine levels can be affected by single nucleotide polymorphism in the gene promoter regions. To investigate whether IL-6 -174 G>C and TNF-α -376 G>A polymorphisms could be correlated to the incidence of FLS, and whether an anti-inflammatory/antipyretic therapy may influence FLS development, a prospective observational study was performed in 190 treatment naïve, multiple sclerosis patients who started IM IFNβ-1a 30mcg once weekly. The identification of IL-6 -174 G>C and TNF-α -376 G>A polymorphisms was achieved by performing an amplification-refractory mutation system. Serum IL-6 levels were measured using enzyme-linked immunosorbent assay in blood samples taken before therapy and then after the first and last IFNβ-1a injection of the follow-up. FLS-related symptoms were recorded by patients once per week during the first 12 weeks of therapy into a self-reported diary. We found that patients carrying at least one copy of the C allele at position -174 in the promoter of IL-6 gene produced lower levels of IL-6 and were less prone to develop FLS, which was also less severe. On the contrary, the polymorphism of TNF-α had no effect on FLS. Patients taking the first dose of anti-inflammatory/antipyretic therapy in the peri-injection period (within 1 hour) experienced a reduced FLS severity. In conclusion, the study of IL-6 -174 G>C polymorphism would allow the identification of patients lacking the C nucleotide on both alleles who are at risk of a more severe FLS, and may be addressed to a timely and stronger anti-inflammatory/antipyretic therapy for a more effective FLS prevention.
机译:干扰素β(IFNβ)治疗多发性硬化症最常见的不良事件之一是流感样综合征(FLS),据报道,它与细胞因子(如白介素6(IL-6)和肿瘤坏死因子- α(TNF-α)。基因启动子区域中的单核苷酸多态性会影响平均细胞因子水平。为了研究IL-6 -174 G> C和TNF-α-376 G> A多态性是否与FLS的发生有关,以及抗炎/退热疗法是否会影响FLS的发展,进行了一项前瞻性观察性研究在190名未接受过治疗的多发性硬化症患者中,每周一次开始IMIFNβ-1a30mcg。 IL-6 -174 G> C和TNF-α-376 G> A多态性的鉴定是通过进行扩增-不应突变系统来实现的。在治疗前以及随后的第一次和最后一次IFNβ-1a注射后,使用酶联免疫吸附测定法测量血液样本中的血清IL-6水平。患者在治疗的前12周内每周一次将FLS相关症状记录在一份自我报告的日记中。我们发现,在IL-6基因启动子的-174位携带至少一个C等位基因拷贝的患者产生的IL-6水平较低,不易发展FLS,病情也较轻。相反,TNF-α的多态性对FLS没有影响。在围注射期(1小时内)服用第一剂抗炎/解热疗法的患者的FLS严重程度降低。总之,对IL-6 -174 G> C多态性的研究将有助于鉴定两个等位基因中缺乏C核苷酸的患者,这些等位基因有更严重的FLS风险,并可能针对及时而更强的抗炎作用/解热疗法可更有效地预防FLS。

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