首页> 外文期刊>Journal of Crohn’s & colitis >Serum levels of soluble receptor for advanced glycation endproducts (sRAGE) are higher in ulcerative colitis and correlate with disease activity.
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Serum levels of soluble receptor for advanced glycation endproducts (sRAGE) are higher in ulcerative colitis and correlate with disease activity.

机译:溃疡性结肠炎中晚期糖基化终产物(sRAGE)的可溶性受体血清水平较高,并且与疾病活动相关。

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Interaction of the receptor for advanced glycation endproducts (RAGE) with its ligands results in expression of inflammatory mediators, activation of NF-kappaB, and induction of oxidative stress, all of which have been implicated in the pathogenesis of inflammatory bowel diseases (IBD). Soluble receptor for advanced glycation endproducts (sRAGE) has recently emerged as a reliable biomarker of inflammation in numerous RAGE-mediated disorders. OBJECTIVE: To assess sRAGE levels in adult patients with IBD. METHOD: Serum was collected from adult patients with Crohn's disease (CD, 56 patients), ulcerative colitis (UC, 60 patients), and healthy controls (HC, 113 subjects). Levels of sRAGE were determined by enzyme-linked immunosorbent assay. RESULTS: Serum sRAGE levels were elevated in IBD compared to HC and were higher in UC patients compared to CD and HC. Levels of sRAGE were significantly higher in the serum of UC patients with active disease compared to patients with inactive disease, but no association with the Montreal Classification was evident. Serum sRAGE was lower in CD patients with biological therapies. CONCLUSIONS: These findings suggest that serum levels of sRAGE are altered in patients with intestinal inflammation and may reflect distinct immunoinflammatory pathogenesis of UC and CD.
机译:晚期糖基化终产物(RAGE)受体与其配体的相互作用导致炎症介质的表达,NF-κB的活化和氧化应激的诱导,所有这些都与炎症性肠病(IBD)的发病机理有关。晚期糖基化终产物(sRAGE)的可溶性受体最近已成为许多RAGE介导的疾病中可靠的炎症生物标志物。目的:评估成人IBD患者的sRAGE水平。方法:从成年的克罗恩病(CD,56例),溃疡性结肠炎(UC,60例)和健康对照(HC,113例)的成人患者中收集血清。 sRAGE的水平通过酶联免疫吸附测定来确定。结果:与HC相比,IBD的血清sRAGE水平升高,而与CD和HC相比,UC患者的血清sRAGE水平升高。与无活动性疾病的患者相比,活动性疾病的UC患者血清中的sRAGE水平显着更高,但与蒙特利尔分类法无关。接受生物疗法的CD患者血清sRAGE较低。结论:这些发现表明,肠道炎症患者的血清sRAGE水平发生了改变,可能反映了UC和CD的独特的免疫炎症机制。

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