Real-world clinical outcomes following treatment intensification with GLP-1 RA, OADs or insulin in patients with type 2 diabetes on two oral agents (PATHWAY 2-OADs).


Journal

BMJ open diabetes research & care
ISSN: 2052-4897
Titre abrégé: BMJ Open Diabetes Res Care
Pays: England
ID NLM: 101641391

Informations de publication

Date de publication:
12 2020
Historique:
received: 17 08 2020
revised: 16 11 2020
accepted: 17 11 2020
entrez: 30 12 2020
pubmed: 31 12 2020
medline: 22 6 2021
Statut: ppublish

Résumé

Most patients with type 2 diabetes require sequential addition of glucose-lowering agents to maintain long-term glycemic control. In this retrospective, observational study, we compared intensification with a glucagon-like peptide-1 receptor agonist (GLP-1 RA), oral antidiabetic drugs (OADs), and insulin in patients receiving two OADs, using US electronic health records and claims data. For inclusion, patients in the IBM MarketScan Explorys database were required to have claims for two different OADs in the 180-day baseline period and ≥1 claim for a different OAD/GLP-1 RA/insulin at index date (treatment intensification). Changes in glycated hemoglobin (HbA Significantly more patients intensifying with a GLP-1 RA achieved HbA In propensity score-matched cohorts, GLP-1 RAs demonstrated significant benefits for both glycemic control and weight management over additional OAD(s) or insulin, respectively, indicating that they may represent the optimal choice at these points in the treatment pathway.

Identifiants

pubmed: 33376084
pii: 8/2/e001830
doi: 10.1136/bmjdrc-2020-001830
pmc: PMC7778743
pii:
doi:

Substances chimiques

Hypoglycemic Agents 0
Insulin 0
Glucagon-Like Peptide 1 89750-14-1

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: CD has performed consultancy for AstraZeneca, Bayer AG and Novo Nordisk A/S. ARK and MLW are employees of, and shareholders in, Novo Nordisk A/S. KKM is an employee of Novo Nordisk Global Service Centre India, which is part of Novo Nordisk A/S. IL has performed consultancy for AstraZeneca, Boehringer Ingelheim Pharmaceuticals, Eli Lilly and Company, Intarcia Therapeutics, Janssen Pharmaceuticals, MannKind Corporation, Novo Nordisk A/S, Sanofi, TARGET PharmaSolutions and Valeritas.

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Auteurs

Cyrus Desouza (C)

Division of Diabetes, Endocrinology, and Metabolism, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska, USA cdesouza@unmc.edu.

Andreas R Kirk (AR)

Novo Nordisk A/S, Søborg, Denmark.

Kamal K Mangla (KK)

Novo Nordisk Global Service Centre India Pvt. Ltd, Bangalore, India.

Michael L Wolden (ML)

Novo Nordisk A/S, Søborg, Denmark.

Ildiko Lingvay (I)

Department of Internal Medicine and Population and Data Sciences, University of Texas Southwestern Medical Center, Dallas, Texas, USA.

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Classifications MeSH