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Diabetes Care 28:10-14, 2005
© 2005 by the American Diabetes Association, Inc.


Clinical Care/Education/Nutrition
Original Article

Randomized Controlled Clinical Trial of Glargine Versus Ultralente Insulin in the Treatment of Type 1 Diabetes

Yogish C. Kudva, MD, MBBS1, Ananda Basu, MD1, Gregory D. Jenkins, MS1, Guillermo M. Pons, MD2, Lori L. Quandt, RN1, Julie A. Gebel, RN1, Debra A. Vogelsang, NP2, Steven A. Smith, MD1, Robert A. Rizza, MD1 and William L. Isley, MD1

1 Division of Endocrinology, Mayo Clinic, Rochester, Minnesota
2 Division of Endocrinology, Immanuel St. Joseph’s Clinic, Mayo Health Care System, Mankato, Minnesota

Address correspondence and reprint requests to Yogish C. Kudva, MD, MBBS, W18A, Division of Endocrinology, Diabetes, Nutrition & Metabolism, Mayo Clinic, 200 First St., SW Rochester, MN 55905. E-mail: kudva.yogish{at}mayo.edu

OBJECTIVE—Multiple daily insulin injection programs are commonly accompanied by considerable glycemic variation and hypoglycemia. We conducted a randomized crossover design clinical trial to compare glargine with ultralente insulin as a basal insulin in type 1 diabetes.

RESEARCH DESIGN AND METHODS—To determine whether the use of glargine insulin as a basal insulin would result in a comparable HbA1c and less glycemic variation and hypoglycemia than ultralente insulin, 22 individuals (aged 44 ± 14 years [±SD], 55% men) with type 1 diabetes who were experienced with multiple daily insulin injections and had an HbA1c of <7.8% were randomized in a crossover design to receive either glargine or ultralente as the basal insulin for 4 months. Aspart insulin was used as the prandial insulin. Physicians providing insulin dose adjustment advice were masked to the type of basal insulin.

RESULTS—Treatment with glargine resulted in lower mean HbA1c (6.82 ± 0.13 vs. 7.02 ± 0.13, difference: 0.2 ± 0.08, P = 0.026), less nocturnal variability (plasma glucose 49.06 ± 4.74 vs. 62.36 ± 5.21 mg/dl, P = 0.04), and less hypoglycemia (24.5 ± 2.99 vs. 31.3 ± 4.04 events, P = 0.05), primarily due to less daytime hypoglycemia (P = 0.002). On the other hand, serious hypoglycemia and average glucose concentration measured with continuous subcutaneous glucose monitoring did not differ.

CONCLUSIONS—We conclude that while use of either ultralente or glargine as a basal insulin can result in excellent glycemic control, treatment with glargine is associated with slightly but significantly lower HbA1c and less nocturnal glycemic variability and hypoglycemia.

Abbreviations: CGMS, continuous subcutaneous glucose monitoring


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Copyright © 2005 by the American Diabetes Association.