组织钙保护蛋白在儿童克罗恩病中的作用——一项初步研究

IF 0.9 Q4 GASTROENTEROLOGY & HEPATOLOGY Gastrointestinal disorders (Basel, Switzerland) Pub Date : 2023-01-12 DOI:10.3390/gidisord5010003
E. Szymańska, S. Szymańska, A. Karkucińska-Więckowska, A. Wierzbicka, J. Kierkuś, M. Dądalski
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引用次数: 0

摘要

背景:粪钙保护蛋白(FCP)是一种高度敏感的肠道炎症生物标志物,广泛用于炎症性肠病(IBD)的诊断和监测。肠黏膜钙保护蛋白的免疫组化评价不是诊断标准。因此,本研究的目的是评估组织钙保护蛋白(TCP)作为一种潜在的标志物,为克罗恩病(CD)儿科患者提供更多的见解。方法:测定CD患儿粪便和组织钙保护蛋白水平,并与疾病活动性和患者内镜活检组织病理学改变相关。使用儿童克罗恩病活动性指数(PCDAI)评估疾病活动性;采用ELISA法测定粪钙保护蛋白(FCP)含量。对六个肠段的活检样本进行钙保护蛋白抗原免疫组化(IHC)染色,每高倍视野(HPF)计数TCP细胞的数量。采用非参数统计检验进行数据分析。结果:57例中位年龄为10.5(1-17)岁的CD患儿接受了粪便和组织钙保护蛋白检测。患者PCDAI评分中位数为10 (0 ~ 63.5),FCP中位数为535 (30 ~ 600)μg/g。我们观察到疾病活动性(PCDAI)与炎性病变和隐窝中的FCP、TCP之间的相关性。FCP与TCP、上皮内TCP与PCDAI均无相关性。结论:免疫组化检测肠黏膜钙保护蛋白对评估疾病行为可能是有用的。FCP是IBD诊断、监测和预后的金标准生物标志物,其水平与我们研究组的临床活动密切相关。
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The Usefulness of Tissue Calprotectin in Pediatric Crohn’s Disease—A Pilot Study
Background: Fecal calprotectin (FCP) is a highly sensitive biomarker of intestinal inflammation widely used in diagnostics and monitoring of inflammatory bowel disease (IBD). Immunohistochemical assessment of calprotectin in the bowel mucosa is not a diagnostic standard. Therefore, the aim of this study was to evaluate tissue calprotectin (TCP) as a potential marker providing added insight for pediatric patients with Crohn’s disease (CD). Methods: Fecal and tissue calprotectin were measured in children with CD. The values were correlated with disease activity and histopathological changes of the patients’ endoscopic biopsies. Disease activity was assessed using the Pediatric Crohn’s Disease Activity Index (PCDAI); fecal calprotectin (FCP) was measured with the ELISA test. Immunohistochemical (IHC) staining for calprotectin antigen was performed on the biopsy samples from six bowel segments, and the number of TCP cells was counted per high power field (HPF). Non-parametric statistical tests were used for data analysis. Results: Fifty-seven children with CD with a median age of 10.5 (1–17) years (yrs) were examined for fecal and tissue calprotectin. The patients’ median PCDAI score was 10 (0–63.5), while median FCP was 535 (30–600) μg/g. We observed a correlation between disease activity (PCDAI) and FCP, TCP in inflammatory lesions and in crypts. There was no association either between FCP and TCP or between TCP in epithelium and PCDAI. Conclusion: It seems that IHC detection of calprotectin in bowel mucosa to assess disease behavior may be useful. FCP is a gold-standard biomarker in the diagnosis, monitoring and prognosis of IBD, and its levels correlated well with clinical activity in our study group.
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