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分子方法治疗炎症性肠病的未来。

The future of molecular approaches to inflammatory bowel disease.

机构信息

Mount Sinai Hospital Inflammatory Bowel Disease Group, Dr Zane Cohen Digestive Diseases Clinical Research Centre, University of Toronto, Toronto, Ontario, Canada.

出版信息

Mol Diagn Ther. 2009;13(4):217-23. doi: 10.1007/BF03256328.

DOI:10.1007/BF03256328
PMID:19712002
Abstract

Technological advances in genomics and transcriptomics have resulted in the introduction of molecular tests into the clinical arena. Despite established uses of such tests in the oncology field, their integration into the management of complex diseases has not been widely evaluated. Progress in the field of inflammatory bowel disease (IBD) genetics has been rapid in recent years, and these advances have provided more urgent impetus to investigating the role of molecular tests in IBD. This article summarizes the current state of molecular testing available for IBD, and the potential utility of such tests as research in the area widens.

摘要

基因组学和转录组学的技术进步使得分子检测得以引入临床领域。尽管此类检测在肿瘤学领域的应用已经得到确立,但它们在复杂疾病管理中的整合尚未得到广泛评估。近年来,炎症性肠病 (IBD) 遗传学领域的进展迅速,这些进展为研究分子检测在 IBD 中的作用提供了更迫切的动力。本文总结了目前可用于 IBD 的分子检测方法,以及随着该领域研究的扩大,此类检测的潜在应用。

相似文献

1
The future of molecular approaches to inflammatory bowel disease.分子方法治疗炎症性肠病的未来。
Mol Diagn Ther. 2009;13(4):217-23. doi: 10.1007/BF03256328.
2
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Have genomic discoveries in inflammatory bowel disease translated into clinical progress?炎症性肠病的基因组学发现是否已转化为临床进展?
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[Diagnostic biomarkers in inflammatory bowel disease].[炎症性肠病中的诊断生物标志物]
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Genes (Basel). 2021 Sep 18;12(9):1438. doi: 10.3390/genes12091438.

引用本文的文献

1
Have genomic discoveries in inflammatory bowel disease translated into clinical progress?炎症性肠病的基因组学发现是否已转化为临床进展?
Curr Gastroenterol Rep. 2012 Apr;14(2):139-45. doi: 10.1007/s11894-012-0248-6.

本文引用的文献

1
Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.通过全基因组关联研究发现的1号染色体p36区域和12号染色体q15区域的溃疡性结肠炎风险基因座。
Nat Genet. 2009 Feb;41(2):216-20. doi: 10.1038/ng.275. Epub 2009 Jan 4.
2
Predictors of severe Crohn's disease.重度克罗恩病的预测因素。
Scand J Gastroenterol. 2008 Aug;43(8):948-54. doi: 10.1080/00365520801957149.
3
Predictive value of serologic markers in a population-based Norwegian cohort with inflammatory bowel disease.基于挪威人群的炎症性肠病队列中血清学标志物的预测价值。
Inflamm Bowel Dis. 2009 Mar;15(3):406-14. doi: 10.1002/ibd.20781.
4
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.全基因组关联研究确定了30多个克罗恩病的不同易感基因座。
Nat Genet. 2008 Aug;40(8):955-62. doi: 10.1038/ng.175. Epub 2008 Jun 29.
5
Multigene analysis can discriminate between ulcerative colitis, Crohn's disease, and irritable bowel syndrome.多基因分析能够区分溃疡性结肠炎、克罗恩病和肠易激综合征。
Gastroenterology. 2008 Jun;134(7):1869-81; quiz 2153-4. doi: 10.1053/j.gastro.2008.02.083. Epub 2008 Mar 2.
6
Transcriptomic analysis of intestinal fibrosis-associated gene expression in response to medical therapy in Crohn's disease.克罗恩病中肠道纤维化相关基因表达对药物治疗反应的转录组学分析
Inflamm Bowel Dis. 2008 Sep;14(9):1197-204. doi: 10.1002/ibd.20482.
7
Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease.溃疡性结肠炎的遗传决定因素包括ECM1基因座和与克罗恩病相关的五个基因座。
Nat Genet. 2008 Jun;40(6):710-2. doi: 10.1038/ng.145. Epub 2008 Apr 27.
8
Replication of signals from recent studies of Crohn's disease identifies previously unknown disease loci for ulcerative colitis.克罗恩病近期研究信号的复制确定了溃疡性结肠炎先前未知的疾病位点。
Nat Genet. 2008 Jun;40(6):713-5. doi: 10.1038/ng.148. Epub 2008 Apr 27.
9
From model cell line to in vivo gene expression: disease-related intestinal gene expression in IBD.从模型细胞系到体内基因表达:炎症性肠病中与疾病相关的肠道基因表达
Genes Immun. 2008 Apr;9(3):240-8. doi: 10.1038/gene.2008.11. Epub 2008 Mar 13.
10
Association of IL23R, TNFRSF1A, and HLA-DRB1*0103 allele variants with inflammatory bowel disease phenotypes in the Finnish population.芬兰人群中白细胞介素23受体(IL23R)、肿瘤坏死因子受体超家族成员1A(TNFRSF1A)及人类白细胞抗原DRB1*0103等位基因变异与炎症性肠病表型的关联
Inflamm Bowel Dis. 2008 Aug;14(8):1118-24. doi: 10.1002/ibd.20431.