首页> 外文期刊>Scandinavian journal of clinical and laboratory investigation. >Anti-inflammatory effect of biological treatment in patients with inflammatory bowel diseases: calprotectin and IL-6 changes do not correspond to sRAGE changes.
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Anti-inflammatory effect of biological treatment in patients with inflammatory bowel diseases: calprotectin and IL-6 changes do not correspond to sRAGE changes.

机译:生物治疗炎症性肠病的抗炎作用:钙卫蛋白和IL-6的变化与sRAGE的变化不符。

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AIM: The main objective was to examine the relationship between the soluble receptor for advanced glycation end products (sRAGE) and calprotectin concentrations in faeces and serum of patients with inflammatory bowel diseases (IBD) during biological treatment with infliximab. MATERIALS AND METHODS: A total of 29 IBD patients treated with infliximab were evaluated. Calprotectin and sRAGE in serum and faeces and serum IL-6 and CRP were measured during the induction regimen of infliximab treatment at weeks (W) 0, 2 and 10. RESULTS: At W0, a significant increase in faecal calprotectin was found in IBD compared to healthy persons (690 +/- 696 microg/g and 23 +/- 7 microg/g, respectively, p < 0.001). No clear difference was found in serum sRAGE levels in IBD cohort compared to healthy controls (772 +/- 274 pg/mL and 720 +/- 107 pg/mL, respectively, p = 0.159); however, a significant negative correlation was found between faecal calprotectin levels and serum concentrations of sRAGE in the active IBD cohort (r = -0.518, p = 0.004). In the stool eluates, sRAGE levels were non-measurable. In the group of responders-to-treatment, the initial surge in both faecal and serum calprotectin levels as well as CRP and IL-6 was followed by a significant decrease on W10. Surprisingly, no significant changeovers were seen in serum sRAGE concentrations in responders neither in W2 nor in W10. CONCLUSIONS: Unlike other examined local and systemic inflammatory markers, serum sRAGE did not change during the infliximab treatment, despite the initial correlation with the degree of mucosal inflammation.
机译:目的:主要目的是研究英夫利昔单抗生物治疗过程中炎症性肠病(IBD)患者粪便和血清中晚期糖基化终产物的可溶性受体(sRAGE)与钙卫蛋白浓度之间的关系。材料与方法:共评估了29例英夫利昔单抗治疗的IBD患者。在第0、2和10周的英夫利昔单抗治疗诱导过程中,测量了血清和粪便中的钙卫蛋白和sRAGE以及血清IL-6和CRP。结果:与WBD相比,IBD粪便中钙卫蛋白的含量显着增加对于健康人(分别为690 +/- 696微克/克和23 +/- 7微克/克,p <0.001)。与健康对照组相比,IBD队列的血清sRAGE水平没有明显差异(分别为772 +/- 274 pg / mL和720 +/- 107 pg / mL,p = 0.159);然而,在活跃的IBD人群中,粪便钙卫蛋白水平与血清​​sRAGE浓度之间存在显着的负相关(r = -0.518,p = 0.004)。在粪便洗脱液中,sRAGE水平不可测量。在治疗反应者组中,粪便和血清钙卫蛋白水平以及CRP和IL-6的初始激增随后是W10的显着下降。令人惊讶的是,在第2周和第10周中,应答者的血清sRAGE浓度均未见明显变化。结论:与其他检查的局部和全身炎症标志物不同,英夫利昔单抗治疗期间血清sRAGE并未改变,尽管其与粘膜炎症的程度初步相关。

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