To Örebro University

oru.seÖrebro University Publications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Alterations in the relative abundance of Faecalibacterium prausnitzii correlate with changes in fecal calprotectin in patients with ileal Crohn's disease: a longitudinal study
Örebro University, School of Medical Sciences.ORCID iD: 0000-0002-4329-1659
Örebro University, School of Medical Sciences.ORCID iD: 0000-0002-7173-5579
Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
Earth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland WA, USA.
Show others and affiliations
2019 (English)In: Scandinavian Journal of Gastroenterology, ISSN 0036-5521, E-ISSN 1502-7708, Vol. 54, no 4, p. 577-585Article in journal (Refereed) Published
Abstract [en]

Objectives: Crohn's disease is characterized by a gut dysbiosis with decreased abundance of butyrate producers such as Faecalibacterium prausnitzii. Although F. prausnitzii secretes anti-inflammatory molecules, few studies have addressed the importance of F. prausnitzii in a longitudinal setting. We aimed to examine the relationship between temporal profiles of F. prausnitzii, the C. leptum group, overall butyrate production, and inflammatory activity.

Material and methods: Fecal samples (n = 59) were collected every third month from nine patients with ileal Crohn's disease. The abundance of F. prausnitzii and C. leptum was quantified relative to the total amount of bacteria using quantitative-PCR. To assess butyrate production of gut microbiota, gene copy numbers of the butyryl-CoA:acetate-CoA transferase (BCoAT) gene were quantified by qPCR. The inflammatory activity was defined by fecal (f)-calprotectin.

Results: No correlation between the relative abundance of F. prausnitzii, the C. leptum group, or copy numbers of the BCoAT gene, and f-calprotectin was observed in the total sample set. By analyzing alterations between consecutive samples, a negative correlation between changes in the relative abundance of F. prausnitzii and f-calprotectin was observed (R = -0.39; p = .009). Changes in C. leptum (R = -0.18, p = .23) and number of copies of the BCoAT gene (R = -0.12; p = .42) did not correlate with f-calprotectin.

Conclusions: There was an inverse correlation between temporal changes in the relative abundance of F. prausnitzii, but not overall butyrate producing capacity, and changes in inflammatory activity in ileal Crohn's disease. These findings indicate that F. prausnitzii may play a role in gut homeostasis, even though causality is still to be demonstrated.

Place, publisher, year, edition, pages
Taylor & Francis, 2019. Vol. 54, no 4, p. 577-585
Keywords [en]
Faecalibacterium prausnitzii, Crohn's disease, calprotectin, butyrate, dysbiosis
National Category
Gastroenterology and Hepatology
Identifiers
URN: urn:nbn:se:oru:diva-74541DOI: 10.1080/00365521.2019.1599417ISI: 000468702300001PubMedID: 31104514Scopus ID: 2-s2.0-85066076241OAI: oai:DiVA.org:oru-74541DiVA, id: diva2:1319832
Funder
Swedish Foundation for Strategic Research, RB13-0160Available from: 2019-06-03 Created: 2019-06-03 Last updated: 2025-08-25Bibliographically approved
In thesis
1. Characterising the Phases of Inflammatory Bowel Disease: From Genetic Predisposition to Established Disease
Open this publication in new window or tab >>Characterising the Phases of Inflammatory Bowel Disease: From Genetic Predisposition to Established Disease
2025 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Background: Inflammatory bowel disease (IBD) is a common and lifelong condition, but the phases of IBD development remain poorly understood.

Aims and methods: We aimed to characterise the distinct phases of IBD, encompassing (1) genetic predisposition, (2) preclinical disease, (3) diagnosis, (4) early disease course, and (5) established disease. To this end, we used twin methodology, proteomic profiling and characterisation of the gut microbiome.

Results: In Study I, the heritability was estimated to be 0.78 for Crohn’s disease (CD) and 0.57 for ulcerative colitis (UC). Study II identified protein signatures capable of predicting a future diagnosis of CD (area under the curve [AUC] = 0.77) and UC (AUC = 0.67). Study III revealed a restricted diagnostic potential of gut microbiome signatures for CD (AUC = 0.62) and UC (AUC = 0.59). Study IV yielded a risk score that could predict the future disease course of patients with newly diagnosed UC (AUC = 0.77). Study V was a longitudinal investigation of patients with ileal CD. We observed a negative correlation between temporal changes in the relative abundance of the commensal bacteria Faecalibacterium prausnitzii and changes in faecal calprotectin levels (R = -0.39; p = .009).

Conclusions:

1. A strong genetic predisposition to IBD is evident, with markedly higher heritability observed in CD relative to UC.

2. The circulating proteome can be used to prognosticate CD more than 16 years before its diagnosis.

3. The mucosa-associated gut microbiome's diagnostic capacity seems limited.

4. A proteomics-based risk score offers a means of predicting the early disease course of UC.

5. Temporal changes in the relative abundance of F. prausnitzii are associated with changes in inflammatory activity in ileal CD.

Place, publisher, year, edition, pages
Örebro: Örebro University, 2025. p. 93
Series
Örebro Studies in Medicine, ISSN 1652-4063 ; 325
National Category
General Medicine
Identifiers
urn:nbn:se:oru:diva-119660 (URN)9789175296593 (ISBN)9789175296609 (ISBN)
Public defence
2025-05-28, Örebro universitet, Campus USÖ, hörsal X1, Södra Grev Rosengatan 32, Örebro, 13:00 (English)
Opponent
Supervisors
Available from: 2025-03-04 Created: 2025-03-04 Last updated: 2025-08-25Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textPubMedScopus

Authority records

Björkqvist, OlleRepsilber, DirkRangel, IgnacioHalfvarson, Jonas

Search in DiVA

By author/editor
Björkqvist, OlleRepsilber, DirkRangel, IgnacioHalfvarson, Jonas
By organisation
School of Medical Sciences
In the same journal
Scandinavian Journal of Gastroenterology
Gastroenterology and Hepatology

Search outside of DiVA

GoogleGoogle Scholar

doi
pubmed
urn-nbn

Altmetric score

doi
pubmed
urn-nbn
Total: 530 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf