New markers in ulcerative colitis.
Intestinal inflammation
Markers
Ulcerative colitis
Journal
Clinica chimica acta; international journal of clinical chemistry
ISSN: 1873-3492
Titre abrégé: Clin Chim Acta
Pays: Netherlands
ID NLM: 1302422
Informations de publication
Date de publication:
Oct 2019
Oct 2019
Historique:
received:
18
06
2019
revised:
26
07
2019
accepted:
26
07
2019
pubmed:
31
7
2019
medline:
12
2
2020
entrez:
31
7
2019
Statut:
ppublish
Résumé
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).
Identifiants
pubmed: 31361991
pii: S0009-8981(19)31982-5
doi: 10.1016/j.cca.2019.07.033
pii:
doi:
Substances chimiques
Biomarkers
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
141-146Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.