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One-year sustained glycaemic control and less hypoglycaemia with new insulin glargine 300 U/ml compared with 100 U/ml in people with type 2 diabetes using basal plus meal-time insulin: the EDITION 1 12-month randomized trial, including 6-month extension.
Riddle, M C; Yki-Järvinen, H; Bolli, G B; Ziemen, M; Muehlen-Bartmer, I; Cissokho, S; Home, P D.
Afiliação
  • Riddle MC; Department of Medicine, Oregon Health and Science University, Portland, OR, USA.
  • Yki-Järvinen H; Department of Medicine, University of Helsinki, Helsinki, Finland.
  • Bolli GB; Department of Medicine, Perugia University Medical School, Perugia, Italy.
  • Ziemen M; Sanofi-Aventis Deutschland GmbH, Frankfurt am Main, Germany.
  • Muehlen-Bartmer I; Sanofi-Aventis Deutschland GmbH, Frankfurt am Main, Germany.
  • Cissokho S; Keyrus Biopharma, Levallois-Perret, France.
  • Home PD; Department of Medicine, Newcastle University, Newcastle upon Tyne, UK.
Diabetes Obes Metab ; 17(9): 835-42, 2015 Sep.
Article em En | MEDLINE | ID: mdl-25846721
ABSTRACT

AIMS:

To evaluate the maintenance of efficacy and safety of insulin glargine 300 U/ml (Gla-300) versus glargine 100 U/ml (Gla-100) in people with type 2 diabetes mellitus (T2DM) using basal plus meal-time insulin for 12 months in the EDITION 1 trial.

METHODS:

EDITION 1 was a multicentre, randomized, open-label, two-arm, phase IIIa study. Participants completing the initial 6-month treatment period continued to receive Gla-300 or Gla-100, as previously randomized, once daily for a further 6-month open-label extension phase. Changes in glycated haemoglobin (HbA1c) and fasting plasma glucose concentrations, insulin dose, hypoglycaemic events and body weight were assessed.

RESULTS:

Of 807 participants enrolled in the initial phase, 89% (359/404) assigned to Gla-300 and 88% (355/403) assigned to Gla-100 completed 12 months. Glycaemic control was sustained in both groups (mean HbA1c Gla-300, 7.24%; Gla-100, 7.42%), with more sustained HbA1c reduction for Gla-300 at 12 months least squares mean difference Gla-300 vs Gla-100 HbA1c -0.17 [95% confidence interval (CI) -0.30 to -0.05]%. The mean daily basal insulin dose at 12 months was 1.03 U/kg for Gla-300 and 0.90 U/kg for Gla-100. Lower percentages of participants had ≥1 confirmed [≤3.9 mmol/l (≤70 mg/dl)] or severe hypoglycaemic event with Gla-300 than Gla-100 at any time of day [24 h; 86 vs 92%; relative risk 0.94 (95% CI 0.89-0.99)] and during the night [54 vs 65%; relative risk 0.84 (95% CI 0.75-0.94)], while the annualized rates of such hypoglycaemic events were similar. No between-treatment differences in adverse events were apparent.

CONCLUSION:

During 12 months of treatment of T2DM requiring basal and meal-time insulin, glycaemic control was better sustained and fewer individuals reported hypoglycaemia with Gla-300 than with Gla-100. The mean basal insulin dose was higher with Gla-300 compared with Gla-100, but total numbers of hypoglycaemic events and overall tolerability did not differ between treatments.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Insulina Glargina / Hipoglicemia / Hipoglicemiantes / Insulina Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Insulina Glargina / Hipoglicemia / Hipoglicemiantes / Insulina Idioma: En Ano de publicação: 2015 Tipo de documento: Article