Current and emerging biomarkers for ulcerative colitis

被引:9
|
作者
Nowak, Jan K. [1 ]
Kalla, Rahul [2 ]
Satsangi, Jack [3 ,4 ]
机构
[1] Poznan Univ Med Sci, Dept Pediat Gastroenterol & Metab Dis, Poznan, Poland
[2] Univ Edinburgh, Queens Med Res Inst, Ctr Inflammat Res, MRC, Edinburgh, Scotland
[3] Univ Oxford, Nuffield Dept Med, Expt Med Div, Translat Gastroenterol Unit, Oxford, England
[4] John Radcliffe Hosp, Expt Med Div, Translat Gastroenterol Unit, Headley Way, Oxford OX3 9DU, England
关键词
Ulcerative colitis; biomarker; calprotectin; gene expression; inflammatory bowel disease; prognostication; INFLAMMATORY-BOWEL-DISEASE; C-REACTIVE PROTEIN; PRIMARY SCLEROSING CHOLANGITIS; FECAL CALPROTECTIN; CROHNS-DISEASE; ENDOSCOPIC ACTIVITY; DNA METHYLATION; PROGNOSTIC BIOMARKERS; ONCOSTATIN M; SEVERITY;
D O I
10.1080/14737159.2023.2279611
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Introduction: Ulcerative colitis (UC) is a chronic illness requiring lifelong management that could be enhanced by personalizing care using biomarkers.Areas covered: The main biomarker discovery modalities are reviewed, highlighting recent results across the spectrum of applications, including diagnostics (serum anti-alpha v beta 6 antibodies achieving an area under the curve [AUC] = 0.99; serum oncostatin M AUC = 0.94), disease activity assessment (fecal calprotectin and serum trefoil factor 3: AUC > 0.90), prognostication of the need for treatment escalation (whole blood transcriptomic panels and CLEC5A/CDH2 ratio: AUC > 0.90), prediction of treatment response, and early identification of patients with subclinical disease. The use of established biomarkers is discussed, along with new evidence regarding autoantibodies, proteins, proteomic panels, transcriptomic signatures, deoxyribonucleic acid methylation patterns, and UC-specific glycomic and metabolic disturbances.Expert opinion: Novel biomarkers will pave the way for optimized UC care. However, validation, simplification, and direct clinical translation of complex models may prove challenging. Currently, few candidates exist to assess key characteristics, such as UC susceptibility, histological disease activity, drug response, and long-term disease behavior. Further research will likely not only reveal new tools to tackle these issues but also contribute to understanding UC pathogenesis mechanisms.
引用
收藏
页码:1107 / 1119
页数:13
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