Impact of fibre and red/processed meat intake on treatment outcomes among patients with chronic inflammatory diseases initiating biological therapy: A prospective cohort study.

biologic therapy chronic inflammatory disease diet fibre inflammatory bowel disease processed meat red meat rheumatoid arthritis

Journal

Frontiers in nutrition
ISSN: 2296-861X
Titre abrégé: Front Nutr
Pays: Switzerland
ID NLM: 101642264

Informations de publication

Date de publication:
2022
Historique:
received: 04 07 2022
accepted: 20 09 2022
entrez: 31 10 2022
pubmed: 1 11 2022
medline: 1 11 2022
Statut: epublish

Résumé

Biologic disease-modifying drugs have revolutionised the treatment of a number of chronic inflammatory diseases (CID). However, up to 60% of the patients do not have a sufficient response to treatment and there is a need for optimization of treatment strategies. To investigate if the treatment outcome of biological therapy is associated with the habitual dietary intake of fibre and red/processed meat in patients with a CID. In this multicentre prospective cohort study, we consecutively enrolled 233 adult patients with a diagnosis of Crohn's Disease, Ulcerative Colitis, Rheumatoid Arthritis (RA), Axial Spondyloarthritis, Psoriatic Arthritis and Psoriasis, for whom biologic therapy was planned, over a 3 year period. Patients with completed baseline food frequency questionnaires were stratified into a high fibre/low red and processed meat exposed group (HFLM) and an unexposed group (low fibre/high red and processed meat intake = LFHM). The primary outcome was the proportion of patients with a clinical response to biologic therapy after 14-16 weeks of treatment. Of the 193 patients included in our primary analysis, 114 (59%) had a clinical response to biologic therapy. In the HFLM group ( Habitual HFLM intake did not affect the clinical response to biological treatment across CIDs. HFLM diet in RA patients might be associated with better odds for responding to biological treatment, but this would need confirmation in a randomised trial. (clinicaltrials.gov), identifier [NCT03173144].

Sections du résumé

Background UNASSIGNED
Biologic disease-modifying drugs have revolutionised the treatment of a number of chronic inflammatory diseases (CID). However, up to 60% of the patients do not have a sufficient response to treatment and there is a need for optimization of treatment strategies.
Objective UNASSIGNED
To investigate if the treatment outcome of biological therapy is associated with the habitual dietary intake of fibre and red/processed meat in patients with a CID.
Methods UNASSIGNED
In this multicentre prospective cohort study, we consecutively enrolled 233 adult patients with a diagnosis of Crohn's Disease, Ulcerative Colitis, Rheumatoid Arthritis (RA), Axial Spondyloarthritis, Psoriatic Arthritis and Psoriasis, for whom biologic therapy was planned, over a 3 year period. Patients with completed baseline food frequency questionnaires were stratified into a high fibre/low red and processed meat exposed group (HFLM) and an unexposed group (low fibre/high red and processed meat intake = LFHM). The primary outcome was the proportion of patients with a clinical response to biologic therapy after 14-16 weeks of treatment.
Results UNASSIGNED
Of the 193 patients included in our primary analysis, 114 (59%) had a clinical response to biologic therapy. In the HFLM group (
Conclusion UNASSIGNED
Habitual HFLM intake did not affect the clinical response to biological treatment across CIDs. HFLM diet in RA patients might be associated with better odds for responding to biological treatment, but this would need confirmation in a randomised trial.
Trial registration UNASSIGNED
(clinicaltrials.gov), identifier [NCT03173144].

Identifiants

pubmed: 36313095
doi: 10.3389/fnut.2022.985732
pmc: PMC9609158
doi:

Banques de données

ClinicalTrials.gov
['NCT03173144']

Types de publication

Journal Article

Langues

eng

Pagination

985732

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Copyright © 2022 Overgaard, Sørensen, Munk, Nexøe, Glerup, Henriksen, Guldmann, Pedersen, Saboori, Hvid, Dahlerup, Hvas, Jawhara, Andersen, Pedersen, Nielsen, Bergenheim, Brodersen, Heitmann, Halldorsson, Holmskov, Bygum, Christensen, Kjeldsen, Ellingsen and Andersen.

Déclaration de conflit d'intérêts

Author CH has received speaker fee from Takeda Pharma and Tillotts Pharma (unrelated to the present work). The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Silja H Overgaard (SH)

The Molecular Diagnostics and Clinical Research Unit, Departement of Blood Samples, Biochemistry and Immunology, University Hospital of Southern Denmark, Aabenraa, Denmark.
Section for Biostatistics and Evidence-Based Research, The Parker Institute, Bispebjerg and Frederiksberg Hospital, Copenhagen, Denmark.
Department of Regional Health Research, University of Southern Denmark, Odense, Denmark.

Signe B Sørensen (SB)

The Molecular Diagnostics and Clinical Research Unit, Departement of Blood Samples, Biochemistry and Immunology, University Hospital of Southern Denmark, Aabenraa, Denmark.
Department of Molecular Medicine, University of Southern Denmark, Odense, Denmark.

Heidi L Munk (HL)

Research Unit of Rheumatology, Department of Clinical Research, University of Southern Denmark, Odense University Hospital, Odense, Denmark.

Anders B Nexøe (AB)

Department of Molecular Medicine, University of Southern Denmark, Odense, Denmark.
Department of Cancer and Inflammation Research, Odense University Hospital, Odense, Denmark.
Department of Medical Gastroenterology, Odense University Hospital, Odense, Denmark.

Henning Glerup (H)

University Research Clinic for Innovative Patient Pathways, Silkeborg Regional Hospital, Silkeborg, Denmark.

Rikke H Henriksen (RH)

University Research Clinic for Innovative Patient Pathways, Silkeborg Regional Hospital, Silkeborg, Denmark.

Tanja Guldmann (T)

University Research Clinic for Innovative Patient Pathways, Silkeborg Regional Hospital, Silkeborg, Denmark.

Natalia Pedersen (N)

Department of Gastroenterology, Slagelse Hospital, Slagelse, Denmark.

Sanaz Saboori (S)

Department of Gastroenterology, Slagelse Hospital, Slagelse, Denmark.

Lone Hvid (L)

Department of Dermatology and Allergy Centre, Odense University Hospital, Odense, Denmark.

Jens F Dahlerup (JF)

Department of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus, Denmark.

Christian L Hvas (CL)

Department of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus, Denmark.

Mohamad Jawhara (M)

The Molecular Diagnostics and Clinical Research Unit, Departement of Blood Samples, Biochemistry and Immunology, University Hospital of Southern Denmark, Aabenraa, Denmark.
Department of Molecular Medicine, University of Southern Denmark, Odense, Denmark.
Department of Surgery, University Hospital of Southern Denmark, Aabenraa, Denmark.

Karina W Andersen (KW)

The Molecular Diagnostics and Clinical Research Unit, Departement of Blood Samples, Biochemistry and Immunology, University Hospital of Southern Denmark, Aabenraa, Denmark.
Department of Surgery, University Hospital of Southern Denmark, Aabenraa, Denmark.

Andreas K Pedersen (AK)

Department of Research and Learning, University Hospital of Southern Denmark, Aabenraa, Denmark.

Ole H Nielsen (OH)

Department of Gastroenterology, Herlev Hospital, University of Copenhagen, Herlev, Denmark.

Fredrik Bergenheim (F)

Department of Gastroenterology, Herlev Hospital, University of Copenhagen, Herlev, Denmark.

Jacob B Brodersen (JB)

Department of Regional Health Research, University of Southern Denmark, Odense, Denmark.
Department of Gastroenterology, Hospital of Southwest Jutland, Esbjerg, Denmark.

Berit L Heitmann (BL)

Research Unit for Dietary Studies, The Parker Institute, Bispebjerg and Frederiksberg Hospital, Copenhagen, Denmark.
Section for General Practice, Department of Public Health, University of Copenhagen, Copenhagen, Denmark.

Thorhallur I Halldorsson (TI)

Faculty of Food Science and Nutrition, School of Health Sciences, University of Iceland, Reykjavík, Iceland.

Uffe Holmskov (U)

Department of Molecular Medicine, University of Southern Denmark, Odense, Denmark.

Anette Bygum (A)

Department of Dermatology and Allergy Centre, Odense University Hospital, Odense, Denmark.
Clinical Institute, University of Southern Denmark, Odense, Denmark.

Robin Christensen (R)

Section for Biostatistics and Evidence-Based Research, The Parker Institute, Bispebjerg and Frederiksberg Hospital, Copenhagen, Denmark.
Research Unit of Rheumatology, Department of Clinical Research, University of Southern Denmark, Odense University Hospital, Odense, Denmark.

Jens Kjeldsen (J)

Department of Medical Gastroenterology, Odense University Hospital, Odense, Denmark.
Research Unit of Medical Gastroenterology, Department of Clinical Research, University of Southern Denmark, Odense, Denmark.

Torkell Ellingsen (T)

Research Unit of Rheumatology, Department of Clinical Research, University of Southern Denmark, Odense University Hospital, Odense, Denmark.

Vibeke Andersen (V)

The Molecular Diagnostics and Clinical Research Unit, Departement of Blood Samples, Biochemistry and Immunology, University Hospital of Southern Denmark, Aabenraa, Denmark.
Department of Molecular Medicine, University of Southern Denmark, Odense, Denmark.
Open Patient Data Explorative Network, Department of Clinical Research, University of Southern, Odense, Denmark.

Classifications MeSH