GLP-1 based therapies and disease course of inflammatory bowel disease

Background: The disease course of inflammatory bowel disease (IBD) following treatment with glucagon-like peptide (GLP)-1 based therapies is unclear. The aim of this study was to examine the disease course of IBD in patients treated with GLP-1 based therapies compared with treatment with other antid...

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Main Authors: Marie Villumsen, Astrid Blicher Schelde, Espen Jimenez-Solem, Tine Jess, Kristine Højgaard Allin
Format: Article
Language:English
Published: Elsevier 2021-07-01
Series:EClinicalMedicine
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2589537021002595
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spelling doaj-55481676362b458c9d47b0c372bf26762021-07-29T04:23:35ZengElsevierEClinicalMedicine2589-53702021-07-0137100979GLP-1 based therapies and disease course of inflammatory bowel diseaseMarie Villumsen0Astrid Blicher Schelde1Espen Jimenez-Solem2Tine Jess3Kristine Højgaard Allin4Center for Clinical Research and Prevention, Bispebjerg and Frederiksberg Hospital, The Capital Region, Copenhagen, Denmark; Corresponding author at: Center for Clinical Research and Prevention, Bispebjerg and Frederiksberg Hospital, Nordre Fasanvej 57, 2000 Frederiksberg, Denmark.Department of Clinical Pharmacology, Copenhagen University Hospital, Bispebjerg and Frederiksberg, Copenhagen, DenmarkDepartment of Clinical Pharmacology, Copenhagen University Hospital, Bispebjerg and Frederiksberg, Copenhagen, Denmark; Copenhagen Phase IV unit (Phase4CPH), Department of Clinical Pharmacology and Center of Clinical Research and Prevention, Bispebjerg and Frederiksberg Hospital, Copenhagen, DenmarkCenter for Molecular Prediction of Inflammatory Bowel Disease, Department of Clinical Medicine, Aalborg University, Copenhagen, DenmarkCenter for Molecular Prediction of Inflammatory Bowel Disease, Department of Clinical Medicine, Aalborg University, Copenhagen, DenmarkBackground: The disease course of inflammatory bowel disease (IBD) following treatment with glucagon-like peptide (GLP)-1 based therapies is unclear. The aim of this study was to examine the disease course of IBD in patients treated with GLP-1 based therapies compared with treatment with other antidiabetics. Methods: Using nationwide Danish registries, we identified patients with IBD and type 2 diabetes who received antidiabetic treatment between 1 January 2007 and 31 March 2019. The primary outcome was a composite of the need for oral corticosteroids, tumour necrosis factor-α inhibitors, IBD-related hospitalisation, or IBD-related surgery. In the setting of a new-user active comparator design, we used Poisson regression to estimate incidence rate ratios (IRR) comparing treatment with GLP-1 receptor agonists and dipeptidyl peptidase (DPP)-4 inhibitors with other antidiabetic therapies. The analyses were adjusted for age, sex, calendar year, IBD severity, and metformin use. Findings: We identified 3751 patients with a diagnosis of IBD and type 2 diabetes and with a prescription of an antidiabetic drug (GLP-1 receptor agonists/DPP-4 inhibitors: 982 patients; other antidiabetic treatment: 2769 patients). The adjusted IRR of the composite outcome was 0·52 (95% CI: 0·42–0·65) for patients exposed to GLP-1 receptor agonists/DPP-4 inhibitors compared with patients exposed to other antidiabetics. Interpretation: In patients with IBD and type 2 diabetes, we observed a lower risk of adverse clinical events amongst patients treated with GLP-1 based therapies compared with treatment with other antidiabetics. These findings suggest that treatment with GLP-1 based therapies may improve the disease course of IBD.http://www.sciencedirect.com/science/article/pii/S2589537021002595Colitis ulcerativeCrohn's diseaseGlucagon-like-peptide 1 receptor agonistsDipeptidyl peptidase-4 inhibitorsPharmacoepidemiologyPrognosis
collection DOAJ
language English
format Article
sources DOAJ
author Marie Villumsen
Astrid Blicher Schelde
Espen Jimenez-Solem
Tine Jess
Kristine Højgaard Allin
spellingShingle Marie Villumsen
Astrid Blicher Schelde
Espen Jimenez-Solem
Tine Jess
Kristine Højgaard Allin
GLP-1 based therapies and disease course of inflammatory bowel disease
EClinicalMedicine
Colitis ulcerative
Crohn's disease
Glucagon-like-peptide 1 receptor agonists
Dipeptidyl peptidase-4 inhibitors
Pharmacoepidemiology
Prognosis
author_facet Marie Villumsen
Astrid Blicher Schelde
Espen Jimenez-Solem
Tine Jess
Kristine Højgaard Allin
author_sort Marie Villumsen
title GLP-1 based therapies and disease course of inflammatory bowel disease
title_short GLP-1 based therapies and disease course of inflammatory bowel disease
title_full GLP-1 based therapies and disease course of inflammatory bowel disease
title_fullStr GLP-1 based therapies and disease course of inflammatory bowel disease
title_full_unstemmed GLP-1 based therapies and disease course of inflammatory bowel disease
title_sort glp-1 based therapies and disease course of inflammatory bowel disease
publisher Elsevier
series EClinicalMedicine
issn 2589-5370
publishDate 2021-07-01
description Background: The disease course of inflammatory bowel disease (IBD) following treatment with glucagon-like peptide (GLP)-1 based therapies is unclear. The aim of this study was to examine the disease course of IBD in patients treated with GLP-1 based therapies compared with treatment with other antidiabetics. Methods: Using nationwide Danish registries, we identified patients with IBD and type 2 diabetes who received antidiabetic treatment between 1 January 2007 and 31 March 2019. The primary outcome was a composite of the need for oral corticosteroids, tumour necrosis factor-α inhibitors, IBD-related hospitalisation, or IBD-related surgery. In the setting of a new-user active comparator design, we used Poisson regression to estimate incidence rate ratios (IRR) comparing treatment with GLP-1 receptor agonists and dipeptidyl peptidase (DPP)-4 inhibitors with other antidiabetic therapies. The analyses were adjusted for age, sex, calendar year, IBD severity, and metformin use. Findings: We identified 3751 patients with a diagnosis of IBD and type 2 diabetes and with a prescription of an antidiabetic drug (GLP-1 receptor agonists/DPP-4 inhibitors: 982 patients; other antidiabetic treatment: 2769 patients). The adjusted IRR of the composite outcome was 0·52 (95% CI: 0·42–0·65) for patients exposed to GLP-1 receptor agonists/DPP-4 inhibitors compared with patients exposed to other antidiabetics. Interpretation: In patients with IBD and type 2 diabetes, we observed a lower risk of adverse clinical events amongst patients treated with GLP-1 based therapies compared with treatment with other antidiabetics. These findings suggest that treatment with GLP-1 based therapies may improve the disease course of IBD.
topic Colitis ulcerative
Crohn's disease
Glucagon-like-peptide 1 receptor agonists
Dipeptidyl peptidase-4 inhibitors
Pharmacoepidemiology
Prognosis
url http://www.sciencedirect.com/science/article/pii/S2589537021002595
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