Better Glycaemic Control and Less Hypoglycaemia with Insulin Glargine 300 U/mL Vs Glargine 100 U/mL: 1-year Patient-level Meta-analysis of the EDITION Clinical Studies in People with Type 2 Diabetes
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Aims: To investigate the efficacy and safety of insulin glargine 300 U/mL (Gla-300) vs insulin glargine 100 U/mL (Gla-100) over 12 months in a patient-level meta-analysis, using data from the EDITION studies in people with type 2 diabetes (T2DM).
Methods: EDITION 1, 2 and 3 were multicentre, randomized, open-label, 2-arm, parallel-group, treat-to-target phase IIIa studies. Similar study designs and endpoints enabled a meta-analysis to be conducted.
Results: Reductions in glycated haemoglobin (HbA1c) were better sustained over 12 months with Gla-300 than with Gla-100 (least squares [LS] mean difference in change from baseline: -0.10 % [95% confidence interval {CI} -0.18 to -0.02] or -1.09 mmol/mol [95% CI -2.01 to -0.20]; P = .0174). Risk of confirmed (≤3.9 mmol/L) or severe hypoglycaemia was 15% lower with Gla-300 vs Gla-100 at night (relative risk 0.85 [95% CI 0.77-0.92]) and 6% lower at any time of day (relative risk 0.94 [95% CI 0.90-0.98]). Rates of hypoglycaemia were 18% lower with Gla-300 vs Gla-100 at night (rate ratio 0.82 [95% CI 0.67-0.99]), but comparable at any time of day. HbA1c <7.0 % without nocturnal hypoglycaemia was achieved by 24% more participants with Gla-300 than with Gla-100 (relative risk 1.24 [95% CI 1.03-1.50]). Severe hypoglycaemia was rare; in both treatment groups the incidence of events at any time of day was ≤3.6%, while rates were ≤0.08 events per participant-year.
Conclusions: In a broad population of people with T2DM over 12 months, use of Gla-300 provided more sustained glycaemic control and significantly lower hypoglycaemia risk at night and at any time of day compared with Gla-100.
Ilie I, Vonica-Tincu A, Dobrea C, Butuca A, Frum A, Morgovan C Biomedicines. 2024; 12(10).
PMID: 39457586 PMC: 11504911. DOI: 10.3390/biomedicines12102273.
Hong E, Min K, Lim J, Ahn K, Ahn C, Yu J Adv Ther. 2024; 41(5):1967-1982.
PMID: 38512540 PMC: 11052798. DOI: 10.1007/s12325-024-02830-z.
Alhmoud E, Saad M, Omar N Front Endocrinol (Lausanne). 2024; 14:1285147.
PMID: 38313835 PMC: 10836592. DOI: 10.3389/fendo.2023.1285147.
[Injection therapy of diabetes].
Lechleitner M, Roden M, Weitgasser R, Ludvik B, Fasching P, Hoppichler F Wien Klin Wochenschr. 2023; 135(Suppl 1):45-52.
PMID: 37101024 PMC: 10133050. DOI: 10.1007/s00508-023-02171-x.
Proteomic Changes to the Updated Discovery of Engineered Insulin and Its Analogs: Pros and Cons.
Hanif N, Wu H, Xu P, Li Y, Bibi A, Zulfiqar A Curr Issues Mol Biol. 2022; 44(2):867-888.
PMID: 35723344 PMC: 8929101. DOI: 10.3390/cimb44020059.