Tolerability and Effectiveness of Switching to Dulaglutide in Patients With Type 2 Diabetes Inadequately Controlled With Insulin Therapy.


Journal

Frontiers in endocrinology
ISSN: 1664-2392
Titre abrégé: Front Endocrinol (Lausanne)
Pays: Switzerland
ID NLM: 101555782

Informations de publication

Date de publication:
2022
Historique:
received: 21 02 2022
accepted: 12 05 2022
entrez: 5 7 2022
pubmed: 6 7 2022
medline: 7 7 2022
Statut: epublish

Résumé

Glucagon-like peptide 1 (GLP-1) receptor agonists have demonstrated strong glycemic control. However, few studies have investigated the effects of switching from insulin to GLP-1 receptor agonists. We aimed to investigate, using real-world data, whether switching to dulaglutide improves glycemic control in patients with type 2 diabetes mellitus (T2D) inadequately controlled with conventional insulin treatment. We retrospectively evaluated 138 patients with T2D who were switched from insulin to dulaglutide therapy. We excluded 20 patients who dropped out during the follow-up period. The participants were divided into two groups according to whether they resumed insulin treatment at 6 months after switching to a GLP-1 receptor agonist (group I) or not (group II). A multiple logistic regression analysis was performed to evaluate the parameters associated with the risk of resuming insulin after replacement with dulaglutide. Of 118 patients initiated on the GLP-1 receptor agonist, 62 (53%) resumed insulin treatment (group I), and 53 (47%) continued with GLP-1 receptor agonists or switched to oral anti-hypoglycemic agents (group II). Older age, a higher insulin dose, and lower postprandial glucose levels while switching to the GLP-1 receptor agonist were associated with failure to switch to the GLP-1 receptor agonist from insulin. A considerable proportion of patients with T2D inadequately controlled with insulin treatment successfully switched to the GLP-1 receptor agonist. Younger age, a lower dose of insulin, and a higher baseline postprandial glucose level may be significant predictors of successful switching from insulin to GLP-1 receptor agonist therapy.

Identifiants

pubmed: 35784534
doi: 10.3389/fendo.2022.880164
pmc: PMC9248324
doi:

Substances chimiques

Blood Glucose 0
Glucagon-Like Peptide-1 Receptor 0
Immunoglobulin Fc Fragments 0
Insulin 0
Recombinant Fusion Proteins 0
Glucagon-Like Peptides 62340-29-8
dulaglutide WTT295HSY5

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

880164

Informations de copyright

Copyright © 2022 Kim, Huh, Lee, Kang, Cha and Lee.

Déclaration de conflit d'intérêts

The 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

Youngsook Kim (Y)

Division of Endocrinology and Metabolism, Department of Internal Medicine, Yonsei, University College of Medicine, Seoul, South Korea.

Ji Hye Huh (JH)

Division of Endocrinology and Metabolism, Department of Internal Medicine, Hallym University Sacred Heart Hospital, Anyang, South Korea.

Minyoung Lee (M)

Division of Endocrinology and Metabolism, Department of Internal Medicine, Yonsei, University College of Medicine, Seoul, South Korea.

Eun Seok Kang (ES)

Division of Endocrinology and Metabolism, Department of Internal Medicine, Yonsei, University College of Medicine, Seoul, South Korea.

Bong-Soo Cha (BS)

Division of Endocrinology and Metabolism, Department of Internal Medicine, Yonsei, University College of Medicine, Seoul, South Korea.

Byung-Wan Lee (BW)

Division of Endocrinology and Metabolism, Department of Internal Medicine, Yonsei, University College of Medicine, Seoul, South Korea.

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Classifications MeSH