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Factors predicting the therapeutic response to infliximab during maintenance therapy in Japanese patients with Crohn’s disease

机译:预测日本克罗恩病患者维持治疗期间对英夫利昔单抗治疗反应的因素

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摘要

Since anti-tumor necrosis factor (TNF)-α agents (TNF-α inhibitors) induce both clinical response and remission in patients with moderate to severe inflammatory bowel disease (IBD), the use of anti-TNF therapies has fundamentally changed the approach to treatment for patients with IBD. Infliximab (IFX) is a TNF-α inhibitor approved for the induction and remission of Crohn’s disease (CD). However, even among patients who initially demonstrate a clinical response to IFX therapy, secondary loss of response occurs, although the reason remains unknown. We therefore investigated predictive factors associated with the response to IFX in long-term maintenance treatment in Japanese CD patients. Eight types of single-nucleotide polymorphisms (SNPs) were investigated using the real-time PCR method, and patient characteristics were collected from the electronic medical records. The Crohn’s Disease Activity Index criteria were used as the response to IFX therapy. The observation period was 1 year after IFX had been administered for more than 1 year. Associations between the IFX response and patient characteristics were evaluated using the multivariate logistic regression model. We studied 121 unrelated adult Japanese with CD treated for more than 1 year with IFX as outpatients at Keio University Hospital from November 1, 2014 to November 30, 2015. Among them, 71 were classified as in remisson. In multivariate analysis, patients with the TNF-α 857C>T C/C genotype, shorter disease duration, without double dosing, and combination treatment with an immunomodulator had higher remisson rates than those with the C/T or T/T genotype, longer disease duration, with double dosing, and no combination treatment with an immunomodulator. The response to IFX in Japanese CD patients may therefore be predicted by these 4 characteristics in actual clinical practice.
机译:由于抗肿瘤坏死因子(TNF)-α药物(TNF-α抑制剂)可诱导中度至重度炎症性肠病(IBD)患者的临床反应和缓解,因此抗TNF治疗的使用从根本上改变了治疗的方法。 IBD患者的治疗。英夫利昔单抗(IFX)是一种被批准用于克罗恩病(CD)诱导和缓解的TNF-α抑制剂。然而,即使在最初对IFX治疗表现出临床反应的患者中,也会出现继发性反应丧失,尽管原因尚不清楚。因此,我们调查了日本CD患者长期维持治疗中与IFX反应相关的预测因素。使用实时PCR方法研究了八种类型的单核苷酸多态性(SNP),并从电子病历中收集了患者特征。将克罗恩病活动指数标准用作对IFX治疗的反应。观察期为IFX给药超过1年后的1年。使用多元逻辑回归模型评估了IFX反应与患者特征之间的关联。我们研究了2014年11月1日至2015年11月30日在庆应义Hospital大学医院作为门诊患者的IFX接受CD治疗1年以上的无关成年日本成年人的情况。其中有71名被归类为缓解。在多变量分析中,与C / T或T / T基因型的患者相比,TNF-α857C> TC / C基因型的患者,疾病持续时间较短,没有双重给药且与免疫调节剂联合治疗的患者具有更高的缓解率。持续时间,双重剂量和不与免疫调节剂联合治疗。因此,可以通过实际临床实践中的这四个特征来预测日本CD患者对IFX的反应。

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