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Dimethyl fumarate in the treatment of relapsing–remitting multiple sclerosis: an overview

机译:富马酸二甲酯治疗复发性多发性硬化症的概述

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摘要

Multiple sclerosis (MS) shares an immune-mediated origin with psoriasis. Long-term safety and efficacy data generated in Europe from usage of fumaric acid formulations in the latter disease constituted grounds to investigate their effects in MS patients. Dimethyl fumarate (DMF) was found to be the active principle in those formulations and in vitro studies have demonstrated that DMF has immune-modulatory properties exerted through abilities to divert cytokine production toward a Th2 profile, both on lymphocytes and microglial cells. More importantly, DMF was discovered to impact the anti-oxidative stress cell machinery promoting the transcription of genes downstream to the activation of the nuclear factor (erythroid derived 2)-like2 (NRF2). DMF exposure increases the cytosol concentrations of NRF2, which besides immune regulatory effects, has the potential for cytoprotection on glial cells, oligodendrocytes and neurons. Extensive and rigorous clinical trials have assessed the efficacy and safety of DMF at the dose of 240 mg twice and three times a day in relapsing-remitting MS patients during one phase IIb and two phase III trials. Robust, positive results were obtained across a number of clinical and paraclinical parameters. In one study (DEFINE), the relative reductions of the adjusted annualized relapse rate of the low and high dose regimens in comparison with placebo were 53% and 48%, respectively (p < 0.001 for both comparisons). In the other trial (CONFIRM), DMF decreased the annualized relapse rate in comparison with placebo by 44% in the lower and by 51% in higher dosage group (also p < 0.001). The number and size of lesions as detected by magnetic resonance imaging were also significantly decreased in comparison with the patients receiving DMF at every dosage. Multiple post hoc and subgroup analyses corroborated the clinical data, rendering DMF an appealing medication whose potential for impacting the degenerative aspects of MS remains to be explored.
机译:多发性硬化症(MS)与牛皮癣共享免疫介导的起源。在欧洲,由于在后者疾病中使用富马酸制剂而产生的长期安全性和有效性数据构成了研究其在MS患者中的作用的基础。富马酸二甲酯(DMF)被发现是这些制剂中的活性成分,体外研究表明,DMF具有免疫调节特性,可通过将淋巴细胞和小胶质细胞上的细胞因子产生转移至Th2谱的能力发挥作用。更重要的是,发现DMF会影响抗氧化应激细胞机制,从而促进下游核因子(类胡萝卜素衍生2)-like2(NRF2)激活基因的转录。暴露于DMF会增加NRF2的胞浆浓度,除了免疫调节作用外,还具有对神经胶质细胞,少突胶质细胞和神经元进行细胞保护的潜力。在一项IIb期和两项III期临床试验中,广泛而严格的临床试验已经评估了DMF在复发缓解型MS患者中每天两次,每天两次240 mg的疗效和安全性。在许多临床和副临床参数中均获得了稳健的积极结果。在一项研究(DEFINE)中,与安慰剂相比,低剂量和高剂量方案的调整后的年复发率分别相对降低了53%和48%(两个比较均p <0.001)。在另一项试验(CONFIRM)中,与安慰剂相比,DMF在较低剂量组中使年复发率降低了44%,而在较高剂量组中则下降了51%(p <0.001)。与在每种剂量下接受DMF的患者相比,通过磁共振成像检测到的病变数量和大小也明显减少。多个事后和亚组分析证实了临床数据,使DMF成为一种有吸引力的药物,其影响MS退行性的潜力仍有待探索。

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