Glucagon-Like Peptide 1 Receptor Agonists and Chronic Lower Respiratory Disease Exacerbations Among Patients With Type 2 Diabetes.


Journal

Diabetes care
ISSN: 1935-5548
Titre abrégé: Diabetes Care
Pays: United States
ID NLM: 7805975

Informations de publication

Date de publication:
06 2021
Historique:
received: 17 07 2020
accepted: 01 03 2021
pubmed: 21 4 2021
medline: 12 11 2021
entrez: 20 4 2021
Statut: ppublish

Résumé

Emerging data from animal and human pilot studies suggest potential benefits of glucagon-like peptide 1 receptor agonists (GLP-1RA) on lung function. We aimed to assess the association of GLP-1RA and chronic lower respiratory disease (CLRD) exacerbation in a population with comorbid type 2 diabetes (T2D) and CLRD. A new-user active-comparator analysis was conducted with use of a national claims database of beneficiaries with employer-sponsored health insurance spanning 2005-2017. We included adults with T2D and CLRD who initiated GLP-1RA or dipeptidyl peptidase 4 inhibitors (DPP-4I) as an add-on therapy to their antidiabetes regimen. The primary outcome was time to first hospital admission for CLRD. The secondary outcome was a count of any CLRD exacerbation associated with an inpatient or outpatient visit. We estimated incidence rates using inverse probability of treatment weighting for each study group and compared via risk ratios. The study sample consisted of 4,150 GLP-1RA and 12,540 DPP-4I new users with comorbid T2D and CLRD. The adjusted incidence rate of first CLRD admission during follow-up was 10.7 and 20.3 per 1,000 person-years for GLP-1RA and DPP-4I users, respectively, resulting in an adjusted hazard ratio of 0.52 (95 GLP-1RA users had fewer CLRD exacerbations in comparison with DPP-4I users. Considering both plausible mechanistic pathways and this real-world evidence, potential beneficial effects of GLP-1RA may be considered in selection of an antidiabetes treatment regimen. Randomized clinical trials are warranted to confirm our findings.

Identifiants

pubmed: 33875487
pii: dc20-1794
doi: 10.2337/dc20-1794
pmc: PMC8247488
doi:

Substances chimiques

Dipeptidyl-Peptidase IV Inhibitors 0
Glucagon-Like Peptide-1 Receptor 0
Hypoglycemic Agents 0
Glucagon-Like Peptide 1 89750-14-1

Banques de données

figshare
['10.2337/figshare.14138138']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1344-1352

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

© 2021 by the American Diabetes Association.

Auteurs

Yasser Albogami (Y)

Department of Pharmaceutical Outcomes & Policy, College of Pharmacy, University of Florida, Gainesville, FL yalbogami@ksu.edu.sa.
Center for Drug Evaluation and Safety, University of Florida, Gainesville, FL.
Department of Clinical Pharmacy, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.

Kenneth Cusi (K)

Division of Endocrinology, Diabetes and Metabolism, University of Florida, Gainesville, FL.

Michael J Daniels (MJ)

Department of Statistics, University of Florida, Gainesville, FL.

Yu-Jung J Wei (YJ)

Department of Pharmaceutical Outcomes & Policy, College of Pharmacy, University of Florida, Gainesville, FL.
Center for Drug Evaluation and Safety, University of Florida, Gainesville, FL.

Almut G Winterstein (AG)

Department of Pharmaceutical Outcomes & Policy, College of Pharmacy, University of Florida, Gainesville, FL.
Center for Drug Evaluation and Safety, University of Florida, Gainesville, FL.

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Classifications MeSH