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炎症性肠病的疾病监测

Disease monitoring in inflammatory bowel disease.

作者信息

Chang Shannon, Malter Lisa, Hudesman David

机构信息

Shannon Chang, Lisa Malter, David Hudesman, Division of Gastroenterology, New York University, New York City, NY 10016, United States.

出版信息

World J Gastroenterol. 2015 Oct 28;21(40):11246-59. doi: 10.3748/wjg.v21.i40.11246.

DOI:10.3748/wjg.v21.i40.11246
PMID:26523100
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4616202/
Abstract

The optimal method for monitoring quiescent disease in patients with Crohn's disease (CD) and ulcerative colitis is yet to be determined. Endoscopic evaluation with ileocolonoscopy is the gold standard but is invasive, costly, and time-consuming. There are many commercially available biomarkers that may be used in clinical practice to evaluate disease status in patients with inflammatory bowel disease (IBD), but the most widely adopted biomarkers are C-reactive protein (CRP) and fecal calprotectin (FC). This review summarizes the evidence for utilizing CRP and FC for monitoring IBD during clinical remission and after surgical resection. Endoscopic correlation with CRP and FC is evaluated in each disease state. Advantages and drawbacks of each biomarker are discussed with special consideration of isolated ileal CD. Fecal immunochemical testing, traditionally used for colorectal cancer screening, is mentioned as a potential new alternative assay in the evaluation of IBD. Based on a mixture of information gleaned from biomarkers, clinical status, and endoscopic evaluation, the best treatment decisions can be made for the patient with IBD.

摘要

监测克罗恩病(CD)和溃疡性结肠炎患者静止期疾病的最佳方法尚未确定。回结肠镜检查的内镜评估是金标准,但具有侵入性、成本高且耗时。有许多可商购的生物标志物可用于临床实践,以评估炎症性肠病(IBD)患者的疾病状态,但应用最广泛的生物标志物是C反应蛋白(CRP)和粪便钙卫蛋白(FC)。本综述总结了在临床缓解期和手术切除后利用CRP和FC监测IBD的证据。在每种疾病状态下评估了CRP和FC与内镜检查的相关性。讨论了每种生物标志物的优缺点,并特别考虑了孤立性回肠CD。传统上用于结直肠癌筛查的粪便免疫化学检测被提及为评估IBD的一种潜在新替代检测方法。基于从生物标志物、临床状态和内镜评估中收集的综合信息,可以为IBD患者做出最佳治疗决策。

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本文引用的文献

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Biomarkers of Inflammation in Inflammatory Bowel Disease.炎症性肠病的炎症生物标志物。
Gastroenterology. 2015 Oct;149(5):1275-1285.e2. doi: 10.1053/j.gastro.2015.07.003. Epub 2015 Jul 9.
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C-Reactive Protein, Fecal Calprotectin, and Stool Lactoferrin for Detection of Endoscopic Activity in Symptomatic Inflammatory Bowel Disease Patients: A Systematic Review and Meta-Analysis.C反应蛋白、粪便钙卫蛋白和粪便乳铁蛋白用于检测有症状炎症性肠病患者的内镜活动:一项系统评价和荟萃分析。
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Evaluation of Mucosal Healing in Ulcerative Colitis by Fecal Calprotectin Vs. Fecal Immunochemical Test.通过粪便钙卫蛋白与粪便免疫化学检测评估溃疡性结肠炎的黏膜愈合情况
Am J Gastroenterol. 2015 Jun;110(6):873-80. doi: 10.1038/ajg.2015.66. Epub 2015 Mar 31.
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Serial fecal calprotectin measurements to detect endoscopic recurrence in postoperative Crohn's disease: is colonoscopic surveillance no longer needed?连续检测粪便钙卫蛋白以发现克罗恩病术后内镜复发:结肠镜监测是否不再必要?
Gastroenterology. 2015 May;148(5):889-92. doi: 10.1053/j.gastro.2015.03.022. Epub 2015 Mar 21.
5
High within-day variability of fecal calprotectin levels in patients with active ulcerative colitis: what is the best timing for stool sampling?活动期溃疡性结肠炎患者粪便钙卫蛋白水平日内变异性高:粪便采样的最佳时间是什么?
Inflamm Bowel Dis. 2015 May;21(5):1072-6. doi: 10.1097/MIB.0000000000000349.
6
Levels of Fecal Calprotectin Are Associated With the Severity of Postoperative Endoscopic Recurrence in Asymptomatic Patients With Crohn's Disease.粪便钙卫蛋白水平与无症状克罗恩病患者术后内镜复发的严重程度相关。
Am J Gastroenterol. 2015 Jun;110(6):865-72. doi: 10.1038/ajg.2015.30. Epub 2015 Mar 17.
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Fecal calprotectin concentrations in healthy children aged 1-18 months.1至18个月健康儿童的粪便钙卫蛋白浓度
PLoS One. 2015 Mar 5;10(3):e0119574. doi: 10.1371/journal.pone.0119574. eCollection 2015.
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Disease activity assessment in IBD: clinical indices and biomarkers fail to predict endoscopic remission.炎症性肠病的疾病活动度评估:临床指标和生物标志物无法预测内镜缓解。
Inflamm Bowel Dis. 2015 Apr;21(4):824-31. doi: 10.1097/MIB.0000000000000341.
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Intestinal stricture in Crohn's disease.克罗恩病中的肠道狭窄
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Pharmacological intervention based on fecal calprotectin levels in patients with ulcerative colitis at high risk of a relapse: A prospective, randomized, controlled study.基于粪钙卫蛋白水平的药物干预在溃疡性结肠炎高复发风险患者中的前瞻性、随机、对照研究。
United European Gastroenterol J. 2015 Feb;3(1):72-9. doi: 10.1177/2050640614560785.