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GLP-1 based therapies and disease course of inflammatory bowel disease
- Source :
- EClinicalMedicine, Vol 37, Iss, Pp 100979-(2021), Villumsen, M, Schelde, A B, Jimenez-Solem, E, Jess, T & Allin, K H 2021, ' GLP-1 based therapies and disease course of inflammatory bowel disease ', EClinicalMedicine, vol. 37, 100979 . https://doi.org/10.1016/j.eclinm.2021.100979, EClinicalMedicine
- Publication Year :
- 2021
- Publisher :
- Elsevier, 2021.
-
Abstract
- Background: The disease course of inflammatory bowel disease (IBD) following treatment with glucagon-like peptide (GLP)-1 based therapies is unclear. Objectives: To examine clinical outcomes of IBD in patients with IBD and type 2 diabetes 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 (IRRs) 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. Results: 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. Conclusion: In patients with IBD and type 2 diabetes, treatment with GLP-1 receptor agonists/DPP-4 inhibitors are associated with a lower risk of adverse clinical events compared with treatment with other antidiabetics. Funding Information: The study was funded by the Novo Nordisk Foundation [grant number NNF16OC0022586 and NNF17OC0029768]. Declaration of Interests: None of the authors have any conflicts of interest to disclose. Ethics Approval Statement: The study was approved by the Danish Data Protection Agency, and data were analysed on a secure research server at the Danish Health Data Authority. In Denmark, ethical approval is not required for research using pre-existing, routinely collected data.
- Subjects :
- Drug
medicine.medical_specialty
Medicine (General)
IMID, immune-mediated inflammatory disease
media_common.quotation_subject
Colitis ulcerative
GLP, glucagon-like-peptide
Type 2 diabetes
SGLT2, Sodium-glucose Cotransporter-2
Lower risk
01 natural sciences
TNF, tumour necrosis factor
Inflammatory bowel disease
03 medical and health sciences
0302 clinical medicine
R5-920
Internal medicine
Dipeptidyl peptidase-4 inhibitors
medicine
030212 general & internal medicine
0101 mathematics
Medical prescription
media_common
Glucagon-like-peptide 1 receptor agonists
ATC, Anatomical Therapeutic Chemical
Crohn's disease
IBD, inflammatory bowel disease
business.industry
Pharmacoepidemiology
010102 general mathematics
General Medicine
medicine.disease
Prognosis
Ulcerative colitis
PY, person-years
ICD, International Classification of Diseases
IR, incidence rate
Metformin
UC, ulcerative colitis
IRR, incidence rate ratios
DPP, dipeptidyl peptidase
CD, Crohn's disease
business
Research Paper
medicine.drug
Subjects
Details
- Language :
- English
- ISSN :
- 25895370
- Volume :
- 37
- Database :
- OpenAIRE
- Journal :
- EClinicalMedicine
- Accession number :
- edsair.doi.dedup.....2d588da1ce421d40f30054039e714cee
- Full Text :
- https://doi.org/10.1016/j.eclinm.2021.100979