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本文引用的文献

1
Indeterminate colitis.不确定性结肠炎。
J Clin Pathol. 2004 Dec;57(12):1233-44. doi: 10.1136/jcp.2003.015214.
2
Gene expression in mononuclear cells from patients with inflammatory bowel disease.炎症性肠病患者单核细胞中的基因表达。
Clin Immunol. 2004 Sep;112(3):247-57. doi: 10.1016/j.clim.2004.03.014.
3
Peripheral blood mononuclear cell fatty acid composition and inflammatory mediator production in adult Crohn's disease.成年克罗恩病患者外周血单个核细胞脂肪酸组成及炎症介质生成情况
Clin Nutr. 2004 Aug;23(4):647-55. doi: 10.1016/j.clnu.2003.10.017.
4
Platelets in inflammatory bowel disease: clinical, pathogenic, and therapeutic implications.炎症性肠病中的血小板:临床、致病及治疗意义
Am J Gastroenterol. 2004 May;99(5):938-45. doi: 10.1111/j.1572-0241.2004.04129.x.
5
Inflammatory bowel disease (ulcerative colitis and Crohn's disease): diagnostic criteria and differential diagnosis.炎症性肠病(溃疡性结肠炎和克罗恩病):诊断标准与鉴别诊断
Drugs Today (Barc). 1998 Nov;34(11):935-42. doi: 10.1358/dot.1998.34.11.487477.
6
Surrogate tissue analysis: monitoring toxicant exposure and health status of inaccessible tissues through the analysis of accessible tissues and cells.替代组织分析:通过分析可获取的组织和细胞来监测难以获取的组织的毒物暴露和健康状况。
Toxicol Appl Pharmacol. 2004 Jan 15;194(2):189-99. doi: 10.1016/j.taap.2003.09.005.
7
Systemic antibodies towards mucosal bacteria in ulcerative colitis and Crohn's disease differentially activate the innate immune response.溃疡性结肠炎和克罗恩病中针对黏膜细菌的全身抗体对先天免疫反应的激活作用存在差异。
Gut. 2004 Jan;53(1):91-8. doi: 10.1136/gut.53.1.91.
8
Disease-associated expression profiles in peripheral blood mononuclear cells from patients with advanced renal cell carcinoma.晚期肾细胞癌患者外周血单个核细胞中与疾病相关的表达谱
Cancer Res. 2003 Sep 15;63(18):6069-75.
9
The immunological and genetic basis of inflammatory bowel disease.炎症性肠病的免疫学和遗传学基础。
Nat Rev Immunol. 2003 Jul;3(7):521-33. doi: 10.1038/nri1132.
10
How could pathologists improve the initial diagnosis of colitis? Evidence from an international workshop.病理学家如何改善结肠炎的初始诊断?来自一次国际研讨会的证据。
J Clin Pathol. 2002 Dec;55(12):955-60. doi: 10.1136/jcp.55.12.955.

利用外周血单核细胞转录谱对克罗恩病和溃疡性结肠炎患者进行分子分类

Molecular classification of Crohn's disease and ulcerative colitis patients using transcriptional profiles in peripheral blood mononuclear cells.

作者信息

Burczynski Michael E, Peterson Ron L, Twine Natalie C, Zuberek Krystyna A, Brodeur Brendan J, Casciotti Lori, Maganti Vasu, Reddy Padma S, Strahs Andrew, Immermann Fred, Spinelli Walter, Schwertschlag Ulrich, Slager Anna M, Cotreau Monette M, Dorner Andrew J

机构信息

Molecular Profiling and Biomarker Discovery/Biomarker Laboratory, Wyeth Research, 500 Arcola Rd., Collegeville PA 19426, USA.

出版信息

J Mol Diagn. 2006 Feb;8(1):51-61. doi: 10.2353/jmoldx.2006.050079.

DOI:10.2353/jmoldx.2006.050079
PMID:16436634
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1867573/
Abstract

Ulcerative colitis (UC) and Crohn's disease (CD) are common inflammatory bowel diseases producing intestinal inflammation and tissue damage. Although emerging evidence suggests these diseases are distinct, approximately 10% of patients remain classified as indeterminate inflammatory bowel disease even after invasive colonoscopy intended for diagnosis. A molecular diagnostic assay using a clinically accessible tissue would greatly assist in the classification of these diseases. In the present study we assessed transcriptional profiles in peripheral blood mononuclear cells from 42 healthy individuals, 59 CD patients, and 26 UC patients by hybridization to microarrays interrogating more than 22,000 sequences. Supervised analysis identified a set of 12 genes that distinguished UC and CD patient samples with high accuracy. The alterations in transcript levels observed by microarray were verified by real-time polymerase chain reaction. The results suggest that a peripheral blood mononuclear cell-based gene expression signature can provide a molecular biomarker that can complement the standard diagnosis of UC and CD.

摘要

溃疡性结肠炎(UC)和克罗恩病(CD)是常见的炎症性肠病,会引发肠道炎症和组织损伤。尽管新出现的证据表明这些疾病有所不同,但即使在进行了旨在诊断的侵入性结肠镜检查后,仍有大约10%的患者被归类为不确定性炎症性肠病。使用临床可获取组织的分子诊断检测方法将极大地有助于这些疾病的分类。在本研究中,我们通过与检测超过22000个序列的微阵列杂交,评估了42名健康个体、59名CD患者和26名UC患者外周血单个核细胞中的转录谱。监督分析确定了一组12个基因,可高精度地区分UC和CD患者样本。通过实时聚合酶链反应验证了微阵列观察到的转录水平变化。结果表明,基于外周血单个核细胞的基因表达特征可以提供一种分子生物标志物,补充UC和CD的标准诊断。