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Characterization of Serum Cytokine Profile in Predominantly Colonic Inflammatory Bowel Disease to Delineate Ulcerative and Crohn’s Colitides

机译:表征主要为结肠炎性肠病的血清细胞因子谱,以描绘溃疡性和克罗恩氏结肠炎

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Background: As accessible diagnostic approaches fail to differentiate between ulcerative colitis (UC) and Crohn’s colitis (CC) in one-third of patients with predominantly colonic inflammatory bowel disease (IBD), leading to inappropriate therapy, we aim to investigate the serum cytokine levels in these patients in search of molecular biometric markers delineating UC from CC.Methods: We measured 38 cytokines, chemokines, and growth factors using magnetic-bead-based multiplex immunoassay in 25 UC patients, 28 CC patients, and 30 controls. Our results are compared with those from a review of current literature regarding advances in serum cytokine profiles and associated challenges preventing their use for diagnostic/prognostic purposes.Results: Univariate analysis showed statistically significant increases of eotaxin, GRO, and TNF-α in UC patients compared to controls (Ctrl); interferon γ, interleukin (IL)-6, and IL-7 in CC group compared to Ctrl; and IL-8 in both UC and CC versus Ctrl. No cytokines were found to be different between UC and CC. A generalized linear model identified combinations of cytokines, allowing the identification of UC and CC patients, with area under the curve (AUC) = 0.936, as determined with receiver operating characteristic (ROC) analysis.Conclusions: The current knowledge available about circulating cytokines in IBD is often contradictory. The development of an evidence-based tool using cytokines for diagnostic accuracy is still preliminary.
机译:背景:由于可利用的诊断方法无法区分以结肠炎性肠病(IBD)为主的患者中三分之一的溃疡性结肠炎(UC)和克罗恩氏结肠炎(CC),导致治疗不当,因此我们旨在研究血清细胞因子水平在这些患者中寻找从CC中划定UC的分子生物标志物。方法:我们使用基于磁珠的多重免疫测定法在25例UC患者,28例CC患者和30例对照中测量了38种细胞因子,趋化因子和生长因子。将我们的结果与当前文献中有关血清细胞因子谱的进展以及阻止将其用于诊断/预后目的的相关挑战进行综述的结果进行比较。与控件(Ctrl)相比; CC组的干扰素γ,白介素(IL)-6和IL-7与Ctrl比较;和UC和CC中的IL-8和Ctrl。 UC和CC之间没有发现细胞因子不同。广义线性模型确定了细胞因子的组合,从而可以确定UC和CC患者,曲线下面积(AUC)= 0.936,这是通过接受者工作特征(ROC)分析确定的。 IBD通常是矛盾的。利用细胞因子提高诊断准确性的循证工具仍处于初步开发阶段。

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