Department of Gastroenterology, Tsaritsa Yoanna University Hospital, Medical University of Sofia, Bulgaria.
Clin Chim Acta. 2019 Oct;497:141-146. doi: 10.1016/j.cca.2019.07.033. Epub 2019 Jul 27.
A new target in the treatment of UC is mucosal healing (MH), which is related to long-term remission, reduced rates of hospitalisation, and colectomy. Despite the advantages in the management of UC over the past few decades, much less has been achieved in the diagnosis and monitoring of the disease where colonoscopy remains the "gold standard" method. Therefore, a non-invasive marker correlating with MH is being sought [14]. Non-invasive markers have the potential to avoid invasive diagnostic tests and inhibit potential complications. Although several noninvasive and easily accessible biomarkers for UC are available, their sensitivity and specificity are not adequate to be used as single markers and do not overrule the need for endoscopic evaluation. Consequently, there is still need for new markers of intestinal inflammation in UC. In the current review Based on a literature search using PubMed, we reviewed eight new potential markers in UC studied mainly in the last five years: trefoil factor 3 (TFF3), leucine-rich Α-2 glycoprotein (LRG), high mobility group box 1 protein (HMGB1), soluble ST2 (sST2), B cell-activating factor (BAFF), annexin A1 (ANXA1), matrix metalloproteinases (MMP), and neutrophil gelatinase-associated lipocalin (NGAL).
治疗 UC 的新靶点是黏膜愈合(MH),它与长期缓解、降低住院率和结肠切除术有关。尽管在过去几十年中 UC 的治疗取得了许多进展,但在疾病的诊断和监测方面取得的进展却很少,结肠镜检查仍然是“金标准”方法。因此,正在寻找与 MH 相关的非侵入性标志物[14]。非侵入性标志物有可能避免侵入性诊断测试并抑制潜在的并发症。尽管有几种用于 UC 的非侵入性和易于获取的生物标志物,但它们的灵敏度和特异性不足以用作单一标志物,并且不能排除对内镜评估的需求。因此,UC 仍需要新的肠道炎症标志物。在目前的综述中,我们基于使用 PubMed 进行的文献检索,综述了过去五年中在 UC 中研究的八种新的潜在标志物:三叶因子 3(TFF3)、富含亮氨酸的 Α-2 糖蛋白(LRG)、高迁移率族蛋白 B1(HMGB1)、可溶性 ST2(sST2)、B 细胞激活因子(BAFF)、膜联蛋白 A1(ANXA1)、基质金属蛋白酶(MMP)和中性粒细胞明胶酶相关脂质运载蛋白(NGAL)。