Efficacy and safety of insulin glargine 300 U/mL vs insulin degludec in patients with type 2 diabetes: A randomized, open-label, cross-over study using continuous glucose monitoring profiles.


Journal

Journal of diabetes investigation
ISSN: 2040-1124
Titre abrégé: J Diabetes Investig
Pays: Japan
ID NLM: 101520702

Informations de publication

Date de publication:
Mar 2019
Historique:
received: 25 03 2018
revised: 06 06 2018
accepted: 19 06 2018
pubmed: 28 6 2018
medline: 10 7 2019
entrez: 28 6 2018
Statut: ppublish

Résumé

Compared with glargine 100 U/mL (Gla100), glargine 300 U/mL (Gla300) and degludec (Deg) - the ultralong-acting insulins - reportedly have more stable effects and reduce the risk of hypoglycemia. Currently, they are considered to be the most useful basal insulins. The present study aimed to compare the efficacy and safety of Gla300 and Deg on glycemic control using continuous glucose monitoring. In this single-center, open-label, parallel-group, two-period, cross-over study, 30 patients with type 2 diabetes were randomized to once-daily Gla300 followed by Deg with the same units (n = 15) or vice versa (n = 15). The primary end-points of this study were the mean percentage of time within the target glucose range of 70-180 mg/dL as efficacy and hypoglycemia of <70 mg/dL as safety indicators, as measured using continuous glucose monitoring during each treatment period. The mean percentage of time within the target glucose range was not different between Gla300 and Deg (77.8 ± 19.2 vs 76.9 ± 18.3%, P = 0.848). However, the mean percentage of time of hypoglycemia with Gla300 was significantly lower than that of Deg (1.3 ± 2.7 vs 5.5 ± 6.4%, P = 0.002). In the secondary safety end-points, the mean percentage of time of severe hypoglycemia (<54 mg/dL) or nocturnal hypoglycemia with Gla300 was also significantly lower than that of Deg. The present study showed the comparable efficacy of Gla300 and Deg on glycemic control; however, the risk of hypoglycemia was markedly lower for Gla300 than for Deg.

Identifiants

pubmed: 29947060
doi: 10.1111/jdi.12884
pmc: PMC6400202
doi:

Substances chimiques

Biomarkers 0
Blood Glucose 0
Glycated Hemoglobin A 0
Hypoglycemic Agents 0
Insulin, Long-Acting 0
hemoglobin A1c protein, human 0
Insulin Glargine 2ZM8CX04RZ
insulin degludec 54Q18076QB

Types de publication

Clinical Trial Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

343-351

Informations de copyright

© 2018 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd.

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Auteurs

Yuji Kawaguchi (Y)

Department of Internal Medicine, Minami Osaka Hospital, Osaka, Japan.

Jun Sawa (J)

Department of Internal Medicine, Minami Osaka Hospital, Osaka, Japan.

Noriko Sakuma (N)

Department of Internal Medicine, Minami Osaka Hospital, Osaka, Japan.

Yasuro Kumeda (Y)

Department of Internal Medicine, Minami Osaka Hospital, Osaka, Japan.

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Classifications MeSH