Faecal biomarkers for diagnosis and prediction of disease course in treatment-naïve patients with IBDShow others and affiliations
2024 (English)In: Alimentary Pharmacology and Therapeutics, ISSN 0269-2813, E-ISSN 1365-2036, Vol. 60, no 6, p. 765-777Article in journal (Refereed) Published
Abstract [en]
Background Faecal biomarkers can be used to assess inflammatory bowel disease (IBD). Aim To explore the performance of some promising biomarkers in diagnosing and predicting disease course in IBD. Methods We included 65 patients with treatment-na & iuml;ve, new-onset Crohn's disease (CD), 90 with ulcerative colitis (UC), 67 symptomatic controls (SC) and 41 healthy controls (HC) in this prospective observational study. We analysed faecal samples for calprotectin (FC), myeloperoxidase (MPO), human neutrophil lipocalin (HNL), eosinophil cationic protein ECP and eosinophil-derived neurotoxin (EDN) and compared markers among groups. We assessed the diagnostic capability of biomarkers with receiver operating characteristic curves. Clinical disease course was determined for each patient with IBD and analysed the association with biomarkers by logistic regression. Results All markers were elevated at inclusion in patients with IBD compared with HC (p < 0.001) and SC (p < 0.001). FC (AUC 0.85, 95% CI: 0.79-0.89) and MPO (AUC 0.85, 95% CI: 0.80-0.89) showed the highest diagnostic accuracy in distinguishing IBD from SC. The diagnostic ability of biomarkers differed between IBD subtypes with the highest performance for FC and MPO in CD. The diagnostic accuracy was further improved by combining FC and MPO (p = 0.02). Levels of FC, MPO and HNL at inclusion were predictive of an aggressive disease course with MPO showing the strongest association (p = 0.006). Conclusions This study provides new insight into the diagnostic and prognostic capability of neutrophil and eosinophil biomarkers in IBD and suggests that MPO, alone or in combination with FC, may add to the diagnostic power of faecal biomarkers.
Place, publisher, year, edition, pages
WILEY , 2024. Vol. 60, no 6, p. 765-777
National Category
Gastroenterology and Hepatology
Identifiers
URN: urn:nbn:se:liu:diva-206364DOI: 10.1111/apt.18154ISI: 001270545300001PubMedID: 38997818OAI: oai:DiVA.org:liu-206364DiVA, id: diva2:1889781
Note
Funding Agencies|Swedish Foundation for Strategic Research [RB13-016]; Swedish Research Council [2020- 02021]; Orebro University Hospital Research Foundation [OLL- 890291]; Medical Faculty, Uppsala University, Uppsala, Sweden M.C
2024-08-162024-08-162025-04-14Bibliographically approved