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Terbutaline and the Prevention of Nocturnal Hypoglycemia in Type 1 Diabetes

  1. Benjamin A. Cooperberg, M.D.,
  2. Suzanne M. Breckenridge, M.D.,
  3. Ana Maria Arbelaez, M.D. and
  4. Philip E. Cryer, M.D. (pcryer{at}wustl.edu)
  1. Division of Endocrinology, Metabolism and Lipid Research, Washington University School of Medicine, St. Louis, Missouri, U.S.A

    Abstract

    Objective – Bedtime administration of 5.0 mg of the β2-adrenergic agonist terbutaline prevents nocturnal hypoglycemia but causes morning hyperglycemia in type 1 diabetes. We tested the hypothesis that 2.5 mg of terbutaline prevents nocturnal hypoglycemia without causing morning hyperglycemia.

    Research Design and Methods – Randomized, double blind, crossover pilot study – placebo, terbutaline 2.5 mg, terbutaline 5.0 mg – in 15 patients with type 1 diabetes.

    Results – Mean (±SE) nadir nocturnal plasma glucose concentrations were 87±14 mg/dL following placebo, 100±14 mg/dL following terbutaline 2.5 mg and 122±13 mg/dL following terbutaline 5.0 mg (P<0.05 vs. placebo). Nadir levels were <50 mg/dL in 5, 2 and 0 patients (P<0.05 vs. placebo) respectively. Morning levels were 113±18, 127±17 and 183±19 mg/dL (P<0.02 vs. placebo) respectively.

    Conclusions – Terbutaline may be shown to be effective and safe in the prevention of nocturnal hypoglycemia in type 1 diabetes in a suitably powered randomized controlled trial.

    Footnotes

      • Received March 12, 2008.
      • Accepted August 26, 2008.

    This Article

    1. Diabetes Care
    1. All Versions of this Article:
      1. dc08-0520v1
      2. 31/12/2271 most recent
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