Bridging dose of U-100 glargine with first dose of insulin degludec improves glycaemia in the 48 h after transition in twice-daily glargine users.

basal insulin continuous glucose monitoring (CGM) glycaemic control type 1 diabetes

Journal

Diabetes, obesity & metabolism
ISSN: 1463-1326
Titre abrégé: Diabetes Obes Metab
Pays: England
ID NLM: 100883645

Informations de publication

Date de publication:
28 Feb 2024
Historique:
revised: 01 02 2024
received: 22 11 2023
accepted: 02 02 2024
medline: 29 2 2024
pubmed: 29 2 2024
entrez: 28 2 2024
Statut: aheadofprint

Résumé

To study the effects of a bridging dose of U-100 glargine (U-100G) with the first dose of degludec in type 1 diabetes (T1D) patients transitioning from glargine to degludec, by comparing the glucose metrics 48 h before and after the transition. Patients with T1D on a stable U-100G regimen and with glycated haemoglobin concentration <75 mmol/mol were randomized (double-blind) to one dose of placebo or U-100G with first dose of degludec, administered at 9:00 pm. Patients on once-daily U-100G at baseline received 50% of total U-100G dose (bridging dose), while patients on twice-daily U-100G received 50% of the evening U-100G dose. Participants wore a continuous glucose monitor during the study. Forty participants were randomized, of whom 37 completed the study. The cohort was 65% male, the mean age was 47 years, duration of T1D 22 years, BMI 26 kg/m A subgroup of well-controlled twice-daily U-100G users transitioning to degludec benefited from a 50% bridging dose of evening U-100G with the first dose of degludec in a small pilot study.

Identifiants

pubmed: 38418413
doi: 10.1111/dom.15502
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Novo Nordisk Pharma, NNI Investigator Sponsored Studies Program, Contra

Informations de copyright

© 2024 John Wiley & Sons Ltd.

Références

Heise T, Nosek L, Bottcher SG, Hastrup H, Haahr H. Ultra-long-acting insulin degludec has a flat and stable glucose-lowering effect in type 2 diabetes. Diabetes Obes Metab. 2012;14(10):944-950.
Haahr H, Heise T. A review of the pharmacological properties of insulin degludec and their clinical relevance. Clin Pharmacokinet. 2014;53(9):787-800.
Heise T, Hermanski L, Nosek L, Feldman A, Rasmussen S, Haahr H. Insulin degludec: four times lower pharmacodynamic variability than insulin glargine under steady-state conditions in type 1 diabetes. Diabetes Obes Metab. 2012;14(9):859-864.
Lane W, Bailey TS, Gerety G, et al. Effect of insulin Degludec vs insulin glargine U100 on hypoglycemia in patients with type 1 diabetes: the SWITCH 1 randomized clinical trial. JAMA. 2017;318(1):33-44.
Liu W, Yang X, Huang J. Efficacy and safety of insulin Degludec versus insulin glargine: a systematic review and meta-analysis of fifteen clinical trials. Int J Endocrinol. 2018;2018: 8726046.
Hamamoto Y, Honjo S, Fujimoto K, et al. Basal and bolus insulin dose changes after switching basal insulin to insulin Degludec in patients with type 1 diabetes mellitus: a pilot study. Clin Drug Investig. 2017;37(9):845-852.
Bohn B, Zimmermann A, Wagner C, et al. Real-life experience of patients starting insulin degludec. A multicenter analysis of 1064 subjects from the German/Austrian DPV registry. Diabetes Res Clin Pract. 2017;129:52-58.
Lane WS, Weatherall J, Gundgaard J, Pollock RF. Insulin degludec versus insulin glargine U100 for patients with type 1 or type 2 diabetes in the US: a budget impact analysis with rebate tables. J Med Econ. 2018;21(2):144-151.
Lecumberri E, Ortega M, Iturregui M, Quesada JA, Vazquez C, Orozco D. Quality-of-life and treatment satisfaction in actual clinical practice of patients with type 1 diabetes mellitus (T1DM) and hypoglycemia treated with insulin degludec. Curr Med Res Opin. 2018;34(6):1053-1059.
Heise T, Korsatko S, Nosek L, et al. Steady state is reached within 2-3 days of once-daily administration of degludec, a basal insulin with an ultralong duration of action. J Diabetes. 2016;8(1):132-138.
Lepore M, Pampanelli S, Fanelli C, et al. Pharmacokinetics and pharmacodynamics of subcutaneous injection of long-acting human insulin analog glargine, NPH insulin, and ultralente human insulin and continuous subcutaneous infusion of insulin lispro. Diabetes. 2000;49(12):2142-2148.
Ashwell SG, Gebbie J, Home PD. Optimal timing of injection of once-daily insulin glargine in people with type 1 diabetes using insulin lispro at meal-times. Diabet Med. 2006;23(1):46-52.
Ashwell SG, Gebbie J, Home PD. Twice-daily compared with once-daily insulin glargine in people with type 1 diabetes using meal-time insulin aspart. Diabet Med. 2006;23(8):879-886.

Auteurs

Arthi Thirumalai (A)

Division of Metabolism, Endocrinology and Nutrition, University of Washington, Seattle, Washington, USA.

Jing H Chao (JH)

Division of Metabolism, Endocrinology and Nutrition, University of Washington, Seattle, Washington, USA.

Thanmai Kaleru (T)

Internal Medicine Residency, Trios Health, Kennewick, Washington, USA.

Xiaofu Dong (X)

University of Washington Medicine Diabetes Institute, Seattle, Washington, USA.

Patali Mandava (P)

University of Washington Medicine Diabetes Institute, Seattle, Washington, USA.

Dori Khakpour (D)

University of Washington Medicine Diabetes Institute, Seattle, Washington, USA.

Irl B Hirsch (IB)

Division of Metabolism, Endocrinology and Nutrition, University of Washington, Seattle, Washington, USA.

Classifications MeSH