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
Molecular Profiling and Biomarker Discovery/Biomarker Laboratory, Wyeth Research, 500 Arcola Rd., Collegeville PA 19426, USA.
J Mol Diagn. 2006 Feb;8(1):51-61. doi: 10.2353/jmoldx.2006.050079.
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.
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。