Chen Peng, Zhou Gaoshi, Lin Jingxia, Li Li, Zeng Zhirong, Chen Minhu, Zhang Shenghong
Division of Gastroenterology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Division of Blood Transfusion, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Front Med (Lausanne). 2020 Apr 22;7:123. doi: 10.3389/fmed.2020.00123. eCollection 2020.
Inflammatory bowel disease (IBD), including Crohn's disease and ulcerative colitis, is a chronic, inflammatory disorder of the gastrointestinal tract. As the novel therapeutic goal and biologicals are widely recognized, accurate assessment of disease and prediction of therapeutic response have become a crucial challenge in clinical practice. Also, because of the continuously rising incidence, convenient and economical methods of diagnosis and clinical assessment are urgently needed. Recently, serum biomarkers have made a great progress and become a focus in IBD study because they are non-invasive, convenient, and relatively inexpensive than are markers in biopsy tissue, stool, breath, and other body fluids. To review the available data on serological biomarkers for IBD. We searched PubMed using predefined key words on relevant literatures of serum biomarkers regarding diagnosis, evaluation of therapeutic efficacy, surveillance of disease activity, and assessment of prognosis for IBD. We reviewed serological biomarkers that are well-established and widely used (e.g., C-reactive protein), newly discovered biomarkers (e.g., cytokines, antibodies, and non-coding RNAs), and also recently advancements in serological biomarkers (e.g., metabolomics and proteomics) that are used in different aspects of IBD management. With such a wealth of researches, to date, there are still no ideal serum biomarkers for IBD. Serum profiling and non-coding RNAs are just starting to blossom but reveal great promise for future clinical practice. Combining different biomarkers can be valuable in improving performance of disease evaluation.
炎症性肠病(IBD),包括克罗恩病和溃疡性结肠炎,是一种胃肠道的慢性炎症性疾病。随着新的治疗目标和生物制剂得到广泛认可,准确评估疾病和预测治疗反应已成为临床实践中的一项关键挑战。此外,由于发病率持续上升,迫切需要方便且经济的诊断和临床评估方法。最近,血清生物标志物取得了很大进展,并成为IBD研究的一个焦点,因为它们是非侵入性的,方便,并且比活检组织、粪便、呼气和其他体液中的标志物相对便宜。为了综述IBD血清生物标志物的现有数据。我们使用预定义的关键词在PubMed上搜索了关于血清生物标志物的相关文献,这些文献涉及IBD的诊断、治疗效果评估、疾病活动监测和预后评估。我们综述了已确立且广泛使用的血清生物标志物(例如,C反应蛋白)、新发现的生物标志物(例如,细胞因子、抗体和非编码RNA),以及最近在IBD管理不同方面使用的血清生物标志物(例如,代谢组学和蛋白质组学)的进展。尽管有如此丰富的研究,但迄今为止,仍没有理想的IBD血清生物标志物。血清谱分析和非编码RNA才刚刚起步,但对未来临床实践显示出巨大的前景。联合使用不同的生物标志物对于提高疾病评估的性能可能是有价值的。