Terbutaline and the Prevention of Nocturnal Hypoglycemia in Type 1 Diabetes
- Benjamin A. Cooperberg, M.D.,
- Suzanne M. Breckenridge, M.D.,
- Ana Maria Arbelaez, M.D. and
- Philip E. Cryer, M.D. (pcryer{at}wustl.edu)
- 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
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- Received March 12, 2008.
- Accepted August 26, 2008.
- Copyright © American Diabetes Association














