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首页> 外文期刊>Pathology Research and Practice >Limited clinical significance of tissue calprotectin levels in bowel mucosa for the prediction of complicated course of the disease in children with ulcerative colitis
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Limited clinical significance of tissue calprotectin levels in bowel mucosa for the prediction of complicated course of the disease in children with ulcerative colitis

机译:肠粘膜中组织CalProtectin水平的有限意义,用于预测溃疡性结肠炎患儿疾病的复杂过程

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摘要

Background: Fecal calprotectin (F-CPT) represents one of the most widely used biomarkers for intestinal inflammation. However, the levels may be false negative or false positive in some situations. Aims: To evaluate the usefulness of immunohistochemical (IHC) detection of tissue calprotectin (T-CPT) in bowel mucosa in children with ulcerative colitis (UC). We focused at correlation of T-CPT with levels of F-CPT and endoscopic and microscopic disease activity at the time of diagnosis and tested whether T-CPT could serve as predictor of complicated course of the disease. Methods: Forty-nine children with newly diagnosed UC between 6/2010-1/2018 entered the study. Endoscopic activity was objectified using the Ulcerative Colitis Endoscopic Index of Severity (UCEIS), clinical activity by Pediatric Ulcerative Colitis Activity Index (PUCAI) and microscopic activity by Geboes and Nancy score. The IHC staining for CPT antigen was performed on bioptic samples from 6 bowel segments and the number of CPT + cells were counted per 1HPF. During the minimal follow-up of 12 months we searched for presence of complications. As outcome for Cox regression model we used composite endpoints: A) Acute Severe Colitis, colectomy, anti-TNF treatment; B) systemic corticotherapy; C) systemic 5-aminosalicylic acid therapy. Results: Neither levels of T-CPT nor values of UCEIS, Geboes or Nancy score predicted the given complications. We found F-CPT levels (HR 2.42 and 2.52) and PUCAI > 40 points (HR 2.98) as predictors of time to endpoints B and C. Good correlation was found between T-CPT levels and Geboes score (k = 0.65) and Nancy score (k = 0.62) and modest with F-CPT (k = 0.44), UCEIS (k = 0.38) and PUCAI (k = 0.42). Conclusions: T-CPT correlated well with microscopic scores. F-CPT and PUCAI appear to be better predictors of unfavorable outcome in patients with UC.
机译:背景:粪便酸蛋白酶(F-CPT)代表肠炎最广泛使用的生物标志物之一。然而,在某些情况下,水平可能是假阴性或假阳性。目的:评估免疫组织化学(IHC)检测溃疡性结肠炎(UC)肠粘膜组织CalProtectin(T-CPT)的有用性。我们专注于T-CPT在诊断时与F-CPT水平和内窥镜和微观疾病活动的相关性,并测试T-CPT是否可以作为疾病复杂过程的预测因子。方法:2010年至2010-1 / 2018年间新诊断的UC儿童进入了该研究。内镜活性使用严重程度(UNYIS)的溃疡性结肠炎内窥镜指数,通过易核和南希评分进行小儿溃疡性结肠炎活性指数(PUCAI)和微观活性的临床活性。 CPT抗原的IHC染色在来自6个肠道段的生物光学样品上进行,每1HPF计算CPT +细胞的数量。在最小的随访期间,我们搜索了并发症的存在。作为Cox回归模型的结果,我们使用复合终点:a)急性严重结肠炎,脱乳糖,抗TNF治疗; b)全身性皮质疗法; c)系统性5-氨基水杨酸治疗。结果:既不是T-CPT水平,也不是uceis的价值,盖伯斯或南希评分预测给定的并发症。我们发现F-CPT水平(HR 2.42和2.52)和PUCAI> 40分(HR 2.98),作为端点的预测因子B和C.在T-CPT水平和GEBOES评分(K = 0.65)和南希之间发现了良好的相关性分数(k = 0.62)和F-CPT(k = 0.44),uceis(k = 0.38)和pucai(k = 0.42)。结论:T-CPT与微观评分相关。 F-CPT和PUCAI似乎是UC患者的不利结果的更好预测因素。

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