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基质金属蛋白酶-9和金属蛋白酶组织抑制剂-1作为新诊断溃疡性结肠炎患儿诊断管理标志物是否有用?

Are Matrix Metalloproteinase-9 and Tissue Inhibitor of Metalloproteinase-1 Useful as Markers in Diagnostic Management of Children with Newly Diagnosed Ulcerative Colitis?

作者信息

Czajkowska Aleksandra, Guzinska-Ustymowicz Katarzyna, Pryczynicz Anna, Lebensztejn Dariusz, Daniluk Urszula

机构信息

Department of Pediatrics, Gastroenterology, Hepatology, Nutrition and Allergology, Medical University of Bialystok, 17 Waszyngtona Street, 15-274 Bialystok, Poland.

Department of General Pathomorphology, Medical University of Bialystok, 15-089 Bialystok, Poland.

出版信息

J Clin Med. 2022 May 9;11(9):2655. doi: 10.3390/jcm11092655.

Abstract

Matrix Metaloproteinase-9 (MMP-9) and Tissue Inhibitor of Metaloproteinase-1 (TIMP-1), enzymes involved in tissue remodelling, have been previously reported to be overexpressed in the colonic mucosa of patients with Ulcerative colitis (UC). The aim of this study was to determine the relation of MMP-9 and TIMP-1 with UC phenotypes, the disease activity index and routinely tested inflammatory markers in newly diagnosed paediatric patients. The study group comprised 35 children diagnosed with UC and 20 control groups. Serum and faecal concentrations of MMP-9 and TIMP-1 were estimated using enzyme-like immunosorbent assay kits and correlated to the disease activity index (Paediatric Ulcerative Colitis Activity Index, PUCAI), UC phenotype (Paris Classification), inflammatory markers and endoscopic score (Mayo score). Children with UC presented with significantly higher serum and faecal concentrations of studied markers compared to the control group. Both serums, MMP-9 and TIMP-1, were higher in children with more extended and severe lesions in the colon. Furthermore, serum MMP-9 correlated with the Mayo score, Paris classification and C-reactive protein (CRP) levels. Serum TIMP-1 showed correlation with PUCAI, Paris Classification, CRP levels and the erythrocyte sedimentation rate. Serum and faecal levels of MMP-9 and TIMP-1 are useful in discriminating UC patients and non-invasive assessments of disease phenotypes. It seemed that simultaneous measurement of these proteins in combination with other common markers of inflammation could be applied in clinical practice.

摘要

基质金属蛋白酶-9(MMP-9)和金属蛋白酶组织抑制剂-1(TIMP-1)是参与组织重塑的酶,此前有报道称它们在溃疡性结肠炎(UC)患者的结肠黏膜中过度表达。本研究的目的是确定MMP-9和TIMP-1与UC表型、疾病活动指数以及新诊断的儿科患者常规检测的炎症标志物之间的关系。研究组包括35名诊断为UC的儿童和20名对照组。使用酶联免疫吸附测定试剂盒估计血清和粪便中MMP-9和TIMP-1的浓度,并将其与疾病活动指数(儿童溃疡性结肠炎活动指数,PUCAI)、UC表型(巴黎分类)、炎症标志物和内镜评分(梅奥评分)相关联。与对照组相比,UC患儿的血清和粪便中研究标志物的浓度明显更高。在结肠病变范围更广、更严重的儿童中,血清MMP-9和TIMP-1均较高。此外,血清MMP-9与梅奥评分、巴黎分类和C反应蛋白(CRP)水平相关。血清TIMP-1与PUCAI、巴黎分类、CRP水平和红细胞沉降率相关。血清和粪便中MMP-9和TIMP-1的水平有助于区分UC患者,并对疾病表型进行非侵入性评估。似乎同时检测这些蛋白质并结合其他常见的炎症标志物可应用于临床实践。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1747/9103541/bc4d8d321b1a/jcm-11-02655-g001.jpg

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