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Effects of biphasic, basal-bolus or basal insulin analogue treatments on carotid intima-media thickness in patients with type 2 diabetes mellitus: the randomised Copenhagen Insulin and Metformin Therapy (CIMT) trial.
Lundby-Christensen, Louise; Vaag, Allan; Tarnow, Lise; Almdal, Thomas P; Lund, Søren S; Wetterslev, Jørn; Gluud, Christian; Boesgaard, Trine W; Wiinberg, Niels; Perrild, Hans; Krarup, Thure; Snorgaard, Ole; Gade-Rasmussen, Birthe; Thorsteinsson, Birger; Røder, Michael; Mathiesen, Elisabeth R; Jensen, Tonny; Vestergaard, Henrik; Hedetoft, Christoffer; Breum, Leif; Duun, Elsebeth; Sneppen, Simone B; Pedersen, Oluf; Hemmingsen, Bianca; Carstensen, Bendix; Madsbad, Sten.
Afiliação
  • Lundby-Christensen L; Steno Diabetes Center, Gentofte, Denmark Department of Endocrinology, Hvidovre, Copenhagen University Hospital, Hvidovre, Denmark Copenhagen Trial Unit, Centre for Clinical Intervention Research, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark Department of Paediatrics, Hvidovre,
  • Vaag A; Steno Diabetes Center, Gentofte, Denmark Department of Endocrinology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark University of Copenhagen, Copenhagen, Denmark.
  • Tarnow L; Steno Diabetes Center, Gentofte, Denmark Department of Cardiology, Nephrology and Endocrinology, Nordsjællands University Hospital-Hillerød, Hillerød, Denmark Department of Health, University of Aarhus, Aarhus, Denmark.
  • Almdal TP; Department of Endocrinology, Hvidovre, Copenhagen University Hospital, Hvidovre, Denmark Department of Endocrinology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
  • Lund SS; Steno Diabetes Center, Gentofte, Denmark Boehringer Ingelheim Pharma GmbH & Co KG, Ingelheim, Germany.
  • Wetterslev J; Copenhagen Trial Unit, Centre for Clinical Intervention Research, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
  • Gluud C; Copenhagen Trial Unit, Centre for Clinical Intervention Research, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
  • Boesgaard TW; Steno Diabetes Center, Gentofte, Denmark.
  • Wiinberg N; Department of Physiology and Nuclear Medicine, Frederiksberg, Copenhagen University Hospital, Frederiksberg, Denmark.
  • Perrild H; Department of Endocrinology, Bispebjerg, Copenhagen University Hospital, Copenhagen, Denmark.
  • Krarup T; Department of Endocrinology, Bispebjerg, Copenhagen University Hospital, Copenhagen, Denmark.
  • Snorgaard O; Department of Endocrinology, Hvidovre, Copenhagen University Hospital, Hvidovre, Denmark.
  • Gade-Rasmussen B; Department of Endocrinology, Hvidovre, Copenhagen University Hospital, Hvidovre, Denmark.
  • Thorsteinsson B; University of Copenhagen, Copenhagen, Denmark Department of Cardiology, Nephrology and Endocrinology, Nordsjællands University Hospital-Hillerød, Hillerød, Denmark.
  • Røder M; Department of Cardiology, Nephrology and Endocrinology, Nordsjællands University Hospital-Hillerød, Hillerød, Denmark Department of Medicine, Gentofte, Copenhagen University Hospital, Gentofte, Denmark.
  • Mathiesen ER; Department of Endocrinology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark University of Copenhagen, Copenhagen, Denmark.
  • Jensen T; Department of Endocrinology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
  • Vestergaard H; University of Copenhagen, Copenhagen, Denmark Department of Endocrinology, Herlev, Copenhagen University Hospital, Herlev, Denmark Section of Metabolic Genetics, The Novo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen, Copenhagen, Denmark.
  • Hedetoft C; Department of Medicine, University Hospital Køge, Køge, Denmark.
  • Breum L; Department of Medicine, University Hospital Køge, Køge, Denmark.
  • Duun E; Department of Medicine, Gentofte, Copenhagen University Hospital, Gentofte, Denmark.
  • Sneppen SB; Department of Medicine, Gentofte, Copenhagen University Hospital, Gentofte, Denmark.
  • Pedersen O; Steno Diabetes Center, Gentofte, Denmark University of Copenhagen, Copenhagen, Denmark Section of Metabolic Genetics, The Novo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen, Copenhagen, Denmark.
  • Hemmingsen B; Copenhagen Trial Unit, Centre for Clinical Intervention Research, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark Department of Cardiology, Nephrology and Endocrinology, Nordsjællands University Hospital-Hillerød, Hillerød, Denmark.
  • Carstensen B; Steno Diabetes Center, Gentofte, Denmark.
  • Madsbad S; Department of Endocrinology, Hvidovre, Copenhagen University Hospital, Hvidovre, Denmark University of Copenhagen, Copenhagen, Denmark.
BMJ Open ; 6(2): e008377, 2016 Feb 25.
Article em En | MEDLINE | ID: mdl-26916685
OBJECTIVE: To assess the effect of 3 insulin analogue regimens on change in carotid intima-media thickness (IMT) in patients with type 2 diabetes. DESIGN AND SETTING: Investigator-initiated, randomised, placebo-controlled trial with a 2 × 3 factorial design, conducted at 8 hospitals in Denmark. PARTICIPANTS AND INTERVENTIONS: Participants with type 2 diabetes (glycated haemoglobin (HbA1c) ≥ 7.5% (≥ 58 mmol/mol), body mass index >25 kg/m(2)) were, in addition to metformin versus placebo, randomised to 18 months open-label biphasic insulin aspart 1-3 times daily (n=137) versus insulin aspart 3 times daily in combination with insulin detemir once daily (n=138) versus insulin detemir alone once daily (n=137), aiming at HbA1c ≤ 7.0% (≤ 53 mmol/mol). OUTCOMES: Primary outcome was change in mean carotid IMT (a marker of subclinical cardiovascular disease). HbA1c, insulin dose, weight, and hypoglycaemic and serious adverse events were other prespecified outcomes. RESULTS: Carotid IMT change did not differ between groups (biphasic -0.009 mm (95% CI -0.022 to 0.004), aspart+detemir 0.000 mm (95% CI -0.013 to 0.013), detemir -0.012 mm (95% CI -0.025 to 0.000)). HbA1c was more reduced with biphasic (-1.0% (95% CI -1.2 to -0.8)) compared with the aspart+detemir (-0.4% (95% CI -0.6 to -0.3)) and detemir (-0.3% (95% CI -0.4 to -0.1)) groups (p<0.001). Weight gain was higher in the biphasic (3.3 kg (95% CI 2.7 to 4.0) and aspart+detemir (3.2 kg (95% CI 2.6 to 3.9)) compared with the detemir group (1.9 kg (95% CI 1.3 to 2.6)). Insulin dose was higher with detemir (1.6 IU/kg/day (95% CI 1.4 to 1.8)) compared with biphasic (1.0 IU/kg/day (95% CI 0.9 to 1.1)) and aspart+detemir (1.1 IU/kg/day (95% CI 1.0 to 1.3)) (p<0.001). Number of participants with severe hypoglycaemia and serious adverse events did not differ. CONCLUSIONS: Carotid IMT change did not differ between 3 insulin regimens despite differences in HbA1c, weight gain and insulin doses. The trial only reached 46% of planned sample size and lack of power may therefore have affected our results. TRIAL REGISTRATION NUMBER: NCT00657943.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Espessura Intima-Media Carotídea / Insulina Tipo de estudo: Clinical_trials Limite: Female / Humans / Male / Middle aged País como assunto: Europa Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Espessura Intima-Media Carotídea / Insulina Tipo de estudo: Clinical_trials Limite: Female / Humans / Male / Middle aged País como assunto: Europa Idioma: En Ano de publicação: 2016 Tipo de documento: Article