Proteomics and metabolomics in inflammatory bowel disease

被引:35
作者
Yau, Yunki [1 ,2 ]
Leong, Rupert W. [2 ,3 ]
Zeng, Ming [1 ]
Wasinger, Valerie C. [1 ]
机构
[1] Univ New S Wales, Bioanalyt Mass Spectrometry Facil, Mark Wainwright Analyt Ctr, Sydney, NSW 2052, Australia
[2] Concord Repatriat Gen Hosp, Dept Gastroenterol & Liver Serv, Corcord, Australia
[3] Bankstown Lidcombe Hosp, Dept Gastroenterol, Bankstown, NSW, Australia
关键词
Crohn's disease; inflammatory bowel disease; mass spectrometry; metabolomics; proteomics; ulcerative colitis; TUMOR-NECROSIS-FACTOR; CARCINOEMBRYONIC ANTIGEN CEA; CROHNS-DISEASE; ULCERATIVE-COLITIS; MASS-SPECTROMETRY; SYSTEMS BIOLOGY; FACTOR-ALPHA; DIAGNOSTIC-ACCURACY; SUSCEPTIBILITY LOCI; ESCHERICHIA-COLI;
D O I
10.1111/jgh.12193
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Genome-wide studies in inflammatory bowel disease (IBD) have allowed us to understand Crohn's disease and ulcerative colitis as forms of related autoinflammatory disorders that arise from a multitude of pathogenic origins. Proteomics and metabolomics are the offspring of genomics that possess unprecedented possibilities to characterize unknown pathogenic pathways. It has been about a decade since proteomics was first applied to IBD, and 5 years for metabolomics. These techniques have yielded novel and potentially important findings, but turning these results into beneficial patient outcomes remains challenging. This review recounts the history and context of clinical IBD developments before and after proteomics and metabolomics IBD in this field, discusses the challenges in consolidating high complexity data with physiological understanding, and provides an outlook on the emerging principles that will help interface the bioanalytical laboratory with IBD prognosis.
引用
收藏
页码:1076 / 1086
页数:11
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