4.7 Article

Addition of Liraglutide to Insulin in Patients With Type 1 Diabetes: A Randomized Placebo-Controlled Clinical Trial of 12 Weeks

Journal

DIABETES CARE
Volume 39, Issue 6, Pages 1027-1035

Publisher

AMER DIABETES ASSOC
DOI: 10.2337/dc15-1136

Keywords

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Funding

  1. Endocrine Fellows Foundation
  2. National Institutes of Health
  3. Centers for Disease Control and Prevention
  4. John R. Oishei Foundation
  5. William G. McGowan Charitable Fund
  6. Millard Fillmore Foundation

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OBJECTIVETo investigate whether addition of three different doses of liraglutide to insulin in patients with type 1 diabetes (T1D) results in significant reduction in glycemia, body weight, and insulin dose.RESEARCH DESIGN AND METHODSWe randomized 72 patients (placebo = 18, liraglutide = 54) with T1D to receive placebo and 0.6, 1.2, and 1.8 mg liraglutide daily for 12 weeks.RESULTSIn the 1.2-mg and 1.8-mg groups, the mean weekly reduction in average blood glucose was -0.55 0.11 mmol/L (10 +/- 2 mg/dL) and -0.55 +/- 0.05 mmol/L (10 +/- 1 mg/dL), respectively (P < 0.0001), while it remained unchanged in the 0.6-mg and placebo groups. In the 1.2-mg group, HbA(1c) fell significantly (-0.78 +/- 15%, -8.5 +/- 1.6 mmol/mol, P < 0.01), while it did not in the 1.8-mg group (-0.42 +/- 0.15%, -4.6 +/- 1.6 mmol/mol, P = 0.39) and 0.6-mg group (-0.26 +/- 0.17%, -2.8 +/- 1.9 mmol/mol, P = 0.81) vs. the placebo group (-0.3 +/- 0.15%, -3.3 +/- 1.6 mmol/mol). Glycemic variability was reduced by 5 +/- 1% (P < 0.01) in the 1.2-mg group only. Total daily insulin dose fell significantly only in the 1.2-mg and 1.8-mg groups (P < 0.05). There was a 5 +/- 1 kg weight loss in the two higher-dose groups (P < 0.05) and by 2.7 +/- 0.6 kg (P < 0.01) in the 0.6-mg group vs. none in the placebo group. In the 1.2- and 1.8-mg groups, postprandial plasma glucagon concentration fell by 72 +/- 12% and 47 +/- 12%, respectively (P < 0.05). Liraglutide led to higher gastrointestinal adverse events (P < 0.05) and 1% increases (not significant) in percent time spent in hypoglycemia (<55 mg/dL, 3.05 mmol/L).CONCLUSIONSAddition of 1.2 mg and 1.8 mg liraglutide to insulin over a 12-week period in overweight and obese patients with T1D results in modest reductions of weekly mean glucose levels with significant weight loss, small insulin dose reductions, and frequent gastrointestinal side effects. These findings do not justify the use of liraglutide in all patients with T1D.

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