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8
Gastrointestinal endoscopy biopsy derived proteomic patterns predict indeterminate colitis into ulcerative colitis and Crohn's colitis.胃肠道内镜活检衍生的蛋白质组学模式可预测不确定性结肠炎发展为溃疡性结肠炎和克罗恩氏结肠炎。
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本文引用的文献

1
Inflammatory bowel disease: an expanding global health problem.炎症性肠病:一个日益严重的全球健康问题。
Clin Med Insights Gastroenterol. 2013 Aug 14;6:33-47. doi: 10.4137/CGast.S12731. eCollection 2013.
2
Quantitative whole-body autoradiography, LC-MS/MS and MALDI for drug-distribution studies in biological samples: the ultimate matrix trilogy.用于生物样品中药物分布研究的定量全身放射自显影、液相色谱-串联质谱法和基质辅助激光解吸电离飞行时间质谱法:终极基质三部曲。
Bioanalysis. 2014 Feb;6(3):377-91. doi: 10.4155/bio.13.336.
3
Crohn's disease presenting as enterovesical fistula.以肠膀胱瘘为表现的克罗恩病。
BMJ Case Rep. 2013 Nov 18;2013:bcr2013201899. doi: 10.1136/bcr-2013-201899.
4
Fecal microbiota transplantation for severe enterocolonic fistulizing Crohn's disease.粪便微生物群移植治疗严重的肠-结肠瘘型克罗恩病。
World J Gastroenterol. 2013 Nov 7;19(41):7213-6. doi: 10.3748/wjg.v19.i41.7213.
5
The burden of comedication among patients with inflammatory bowel disease.炎症性肠病患者的共用药负担。
Inflamm Bowel Dis. 2013 Dec;19(13):2725-36. doi: 10.1097/01.MIB.0000435442.07237.a4.
6
Imaging mass spectrometry: a new tool for pathology in a molecular age.成像质谱技术:分子时代病理学的新工具。
Proteomics Clin Appl. 2013 Dec;7(11-12):733-8. doi: 10.1002/prca.201300055.
7
Drug delivery strategies in the therapy of inflammatory bowel disease.炎症性肠病治疗中的药物输送策略。
Adv Drug Deliv Rev. 2014 May;71:58-76. doi: 10.1016/j.addr.2013.10.001. Epub 2013 Oct 22.
8
New mechanisms and targets for IBD Therapy: translational gastroenterology comes of age.炎症性肠病治疗的新机制与靶点:转化胃肠病学走向成熟。
Curr Drug Targets. 2013 Nov;14(12):1377-8. doi: 10.2174/13894501113146660220.
9
Challenging question: can we diagnose Crohn's disease without histology?挑战性问题:我们能否不进行组织学检查而诊断克罗恩病?
Dig Dis. 2013;31(2):202-6. doi: 10.1159/000353368. Epub 2013 Sep 6.
10
Mechanisms of tissue remodeling in inflammatory bowel disease.炎症性肠病中的组织重构机制。
Dig Dis. 2013;31(2):186-93. doi: 10.1159/000353364. Epub 2013 Sep 6.

炎症性肠病的诊断:分子生物标志物的潜在作用。

Diagnosis of inflammatory bowel disease: Potential role of molecular biometrics.

机构信息

Amosy E M'Koma, Department of Biochemistry and Cancer Biology, Meharry Medical College School of Medicine, Nashville, TN 37208-3599, United States.

出版信息

World J Gastrointest Surg. 2014 Nov 27;6(11):208-19. doi: 10.4240/wjgs.v6.i11.208.

DOI:10.4240/wjgs.v6.i11.208
PMID:25429322
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4241488/
Abstract

Accurate diagnosis of predominantly colonic inflammatory bowel disease (IBD) is not possible in 30% of patients. For decades, scientists have worked to find a solution to improve diagnostic accuracy for IBD, encompassing Crohn's colitis and ulcerative colitis. Evaluating protein patterns in surgical pathology colectomy specimens of colonic mucosal and submucosal compartments, individually, has potential for diagnostic medicine by identifying integrally independent, phenotype-specific cellular and molecular characteristics. Mass spectrometry (MS) and imaging (I) MS are analytical technologies that directly measure molecular species in clinical specimens, contributing to the in-depth understanding of biological molecules. The biometric-system complexity and functional diversity is well suited to proteomic and diagnostic studies. The direct analysis of cells and tissues by Matrix-Assisted-Laser Desorption/Ionization (MALDI) MS/IMS has relevant medical diagnostic potential. MALDI-MS/IMS detection generates molecular signatures obtained from specific cell types within tissue sections. Herein discussed is a perspective on the use of MALDI-MS/IMS and bioinformatics technologies for detection of molecular-biometric patterns and identification of differentiating proteins. I also discuss a perspective on the global challenge of transferring technologies to clinical laboratories dealing with IBD issues. The significance of serologic-immunometric advances is also discussed.

摘要

在 30%的患者中,无法准确诊断主要为结肠的炎症性肠病 (IBD)。几十年来,科学家们一直致力于寻找一种解决方案,以提高 IBD 的诊断准确性,包括克罗恩病结肠炎和溃疡性结肠炎。评估结肠黏膜和黏膜下层单独的手术病理学结肠切除标本中的蛋白质模式,通过识别完整独立的、表型特异性的细胞和分子特征,具有诊断医学的潜力。质谱 (MS) 和成像 (I) MS 是直接测量临床标本中分子种类的分析技术,有助于深入了解生物分子。生物计量系统的复杂性和功能多样性非常适合蛋白质组学和诊断研究。基质辅助激光解吸/电离 (MALDI) MS/IMS 直接分析细胞和组织,具有相关的医学诊断潜力。MALDI-MS/IMS 检测生成从组织切片中特定细胞类型获得的分子特征。本文讨论了 MALDI-MS/IMS 和生物信息学技术在检测分子生物计量模式和识别区分蛋白中的应用前景。我还讨论了将技术转移到处理 IBD 问题的临床实验室的全球挑战的前景。还讨论了血清免疫计量学进展的意义。