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Basal insulin peglispro versus insulin glargine in insulin-naïve type 2 diabetes: IMAGINE 2 randomized trial.
Davies, M J; Russell-Jones, D; Selam, J-L; Bailey, T S; Kerényi, Z; Luo, J; Bue-Valleskey, J; Iványi, T; Hartman, M L; Jacobson, J G; Jacober, S J.
Afiliación
  • Davies MJ; Department of Health Sciences, Diabetes Research Centre, University of Leicester, Leicester, UK.
  • Russell-Jones D; Department of Endocrinology and Diabetes, Royal Surrey County Hospital, Guildford, UK.
  • Selam JL; Diabetes Research Center, Tustin, California.
  • Bailey TS; AMCR Institute, Escondido, California.
  • Kerényi Z; Csepel Health Service, Budapest, Hungary.
  • Luo J; Eli Lilly and Company, Indianapolis, Indiana.
  • Bue-Valleskey J; Eli Lilly and Company, Indianapolis, Indiana.
  • Iványi T; Eli Lilly and Company, Budapest, Hungary.
  • Hartman ML; Eli Lilly and Company, Indianapolis, Indiana.
  • Jacobson JG; Eli Lilly and Company, Indianapolis, Indiana.
  • Jacober SJ; Eli Lilly and Company, Indianapolis, Indiana. sjacober@lilly.com.
Diabetes Obes Metab ; 18(11): 1055-1064, 2016 11.
Article en En | MEDLINE | ID: mdl-27349219
AIMS: To compare, in a double-blind, randomized, multi-national study, 52- or 78-week treatment with basal insulin peglispro or insulin glargine, added to pre-study oral antihyperglycaemic medications, in insulin-naïve adults with type 2 diabetes. MATERIAL AND METHODS: The primary outcome was non-inferiority of peglispro to glargine with regard to glycated haemoglobin (HbA1c) reduction (margin = 0.4%). Six gated secondary objectives with statistical multiplicity adjustments focused on other measures of glycaemic control and safety. Liver fat content was measured using MRI, in a subset of patients. RESULTS: Peglispro was non-inferior to glargine in HbA1c reduction [least-squares (LS) mean difference: -0.29%, 95% confidence interval (CI) -0.40, -0.19], and had a lower nocturnal hypoglycaemia rate [relative rate 0.74 (95% CI 0.60, 0.91); p = .005), more patients achieving HbA1c <7.0% without nocturnal hypoglycaemia [odds ratio (OR) 2.15 (95% CI 1.60, 2.89); p < .001], greater HbA1c reduction (p < .001), and more patients achieving HbA1c<7.0% [OR 1.97 (95% CI 1.57, 2.47); p < .001]. Total hypoglycaemia rate and fasting serum glucose did not achieve statistical superiority. At 52 weeks, peglispro-treated patients had higher triglyceride (1.9 vs 1.7 mmol/L). alanine transaminase (34 vs 27 IU/L), and aspartate transaminase levels (27 vs 24 IU/L). LS mean liver fat content was unchanged with peglispro at 52 weeks but decreased 3.1% with glargine [difference: 2.6% (0.9, 4.2); p = .002]. More peglispro-treated patients experienced adverse injection site reactions (3.5% vs 0.6%, p < .001). CONCLUSIONS: Compared with glargine at 52 weeks, peglispro resulted in a statistically superior reduction in HbA1c, more patients achieving HbA1c targets, less nocturnal hypoglycaemia, no improvement in total hypoglycaemia, higher triglyceride levels, higher aminotransferase levels, and more injection site reactions.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polietilenglicoles / Diabetes Mellitus Tipo 2 / Insulina Lispro / Insulina Glargina / Hipoglucemiantes Tipo de estudio: Clinical_trials Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Diabetes Obes Metab Asunto de la revista: ENDOCRINOLOGIA / METABOLISMO Año: 2016 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polietilenglicoles / Diabetes Mellitus Tipo 2 / Insulina Lispro / Insulina Glargina / Hipoglucemiantes Tipo de estudio: Clinical_trials Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Diabetes Obes Metab Asunto de la revista: ENDOCRINOLOGIA / METABOLISMO Año: 2016 Tipo del documento: Article Pais de publicación: Reino Unido