Metformin versus placebo in combination with insulin analogues in patients with type 2 diabetes mellitus-the randomised, blinded Copenhagen Insulin and Metformin Therapy (CIMT) trial

Louise Lundby-Christensen, Lise Tarnow, Trine W Boesgaard, Søren S Lund, Niels Wiinberg, Hans Perrild, Thure Krarup, Ole Snorgaard, Birthe Gade-Rasmussen, Birger Thorsteinsson, Michael Røder, Elisabeth R Mathiesen, Tonny Jensen, Henrik Vestergaard, Christoffer Hedetoft, Leif Breum, Elsebeth Duun, Simone B Sneppen, Oluf Pedersen, Bianca Hemmingsen, Bendix Carstensen, Sten Madsbad, Christian Gluud, Jørn Wetterslev, Allan Vaag, Thomas P Almdal, Louise Lundby-Christensen, Lise Tarnow, Trine W Boesgaard, Søren S Lund, Niels Wiinberg, Hans Perrild, Thure Krarup, Ole Snorgaard, Birthe Gade-Rasmussen, Birger Thorsteinsson, Michael Røder, Elisabeth R Mathiesen, Tonny Jensen, Henrik Vestergaard, Christoffer Hedetoft, Leif Breum, Elsebeth Duun, Simone B Sneppen, Oluf Pedersen, Bianca Hemmingsen, Bendix Carstensen, Sten Madsbad, Christian Gluud, Jørn Wetterslev, Allan Vaag, Thomas P Almdal

Abstract

Objective: To assess the effect of metformin versus placebo both in combination with insulin analogue treatment on changes 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 eight hospitals in Denmark.

Participants and interventions: 412 participants with type 2 diabetes (glycated haemoglobin (HbA1c) ≥ 7.5% (≥ 58 mmol/mol); body mass index >25 kg/m2) were in addition to open-labelled insulin treatment randomly assigned 1:1 to 18 months blinded metformin (1 g twice daily) versus placebo, aiming at an HbA1c ≤ 7.0% (≤ 53 mmol/mol).

Outcomes: The primary outcome was change in the mean carotid IMT (a marker of subclinical cardiovascular disease). HbA1c, insulin dose, weight and hypoglycaemic and serious adverse events were other prespecified outcomes.

Results: Change in the mean carotid IMT did not differ significantly between the groups (between-group difference 0.012 mm (95% CI -0.003 to 0.026), p=0.11). HbA1c was more reduced in the metformin group (between-group difference -0.42% (95% CI -0.62% to -0.23%), p<0.001)), despite the significantly lower insulin dose at end of trial in the metformin group (1.04 IU/kg (95% CI 0.94 to 1.15)) compared with placebo (1.36 IU/kg (95% CI 1.23 to 1.51), p<0.001). The metformin group gained less weight (between-group difference -2.6 kg (95% CI -3.3 to -1.8), p<0.001). The groups did not differ with regard to number of patients with severe or non-severe hypoglycaemic or other serious adverse events, but the metformin group had more non-severe hypoglycaemic episodes (4347 vs 3161, p<0.001).

Conclusions: Metformin in combination with insulin did not reduce carotid IMT despite larger reduction in HbA1c, less weight gain, and smaller insulin dose compared with placebo plus insulin. However, the trial only reached 46% of the planned sample size and lack of power may therefore have affected our results.

Trial registration number: NCT00657943; Results.

Keywords: ULTRASONOGRAPHY.

Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/

Figures

Figure 1
Figure 1
Flow of participants through trial.
Figure 2
Figure 2
Changes in the mean carotid intima-media thickness (IMT) (mean (95% CI)) in the metformin+insulin group (red), placebo+insulin group (blue) group, and the intervention effect (yellow) from the random effects model with baseline as the covariate using multiply imputed data, adjusted for stratification variables.
Figure 3
Figure 3
Changes (mean (95% CI)) during 18 months of intervention with metformin+insulin (red) and placebo+insulin (blue) in HbA1c (A), fasting plasma glucose (B), insulin dose (C), and weight (D). Numbers on the right-hand side of the graphs indicate the absolute/relative changes from trial entry to end of trial.

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