Gut Mycobiome in Inflammatory Bowel Disease: A Systematic Review of Case-Control StudiesShow others and affiliations
2025 (English)In: Inflammatory Bowel Diseases, ISSN 1078-0998, E-ISSN 1536-4844, Vol. 31, no 11, p. 3213-3224Article, review/survey (Refereed) Published
Abstract [en]
BACKGROUND: The bacterial composition of the microbiome in inflammatory bowel disease (IBD) has been the focus of substantial interest. In contrast, the fungal part of the microbiome, the mycobiome, has only rarely been investigated-although anti-Saccharomyces cerevisiae antibodies, an antibody against fungal mannan, have been known for years as a biomarker for Crohn's disease (CD), but not for ulcerative colitis (UC).
METHODS: A systematic review of case-control studies on the human gut mycobiome in IBD was conducted using searches in EMBASE and MEDLINE.
RESULTS: Twenty-seven studies, with a total of 1406 IBD patients and 1060 controls were identified. The differences in alpha diversity varied across studies and were related to geography, whereas differences in beta diversity between cases and controls were found in a large majority of the studies. Overall, the results were inconsistent at different taxonomic levels, and the studied populations were heterogeneous, as were the methodological approaches. The most consistent finding was an increase of Candida for both CD and UC and of Malassezia in CD, where it was often linked to a decrease of Saccharomyces.
CONCLUSIONS: The mycobiome is altered in IBD, as differences in beta diversity were found between cases and controls consistently. Future studies should carefully standardize every step from sample collection through analysis and data processing, allowing external validation of findings. Inclusion of treatment naïve patients and symptomatic controls could further advance this field.
Place, publisher, year, edition, pages
Oxford University Press, 2025. Vol. 31, no 11, p. 3213-3224
Keywords [en]
Crohn’s disease, case-control studies, mycobiome, systematic review, ulcerative colitis
National Category
Gastroenterology and Hepatology
Identifiers
URN: urn:nbn:se:oru:diva-124059DOI: 10.1093/ibd/izaf217ISI: 001577522000001PubMedID: 40990048Scopus ID: 2-s2.0-105022732647OAI: oai:DiVA.org:oru-124059DiVA, id: diva2:2002269
Funder
NordForsk, 90569 NORDTREATThe Research Council of Norway, 2988039Vinnova, 2019-01185 NORDTREATGerman Research Foundation (DFG), EXC 2167German Research Foundation (DFG)
Note
Funding Agencies:
This work was supported by the Odense University Hospital PhD Fund [grant number A5031 to J.D.F.]; NordForsk [grant number 90569 NORDTREAT to J.H.]; Innovation Fund Denmark [grant number 8114-00026B to J.K. and V.A.]; the Research Council of Norway [grant number 2988039 to M.L.H.]; the Vinnova [grant number 2019-01185 NORDTREAT to J.H.]; the Region of Southern Denmark’s Pulje for Fri og Strategisk Forskning [grant number A1381 to J.K. and J.D.F.]; the Deutsche Forschungsgemeinschaft Cluster of Excellence “Precision Medicine in Chronic Inflammation” [EXC 2167]; and the Deutsche Forschungsgemeinschaft Research Unit 5042 miTarget.
2025-09-302025-09-302026-01-23Bibliographically approved