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Diabetes Care 25:883-888, 2002
© 2002 by the American Diabetes Association, Inc.


Pathophysiology/Complications
Original Article

Improved Postprandial Glycemic Control With Biphasic Insulin Aspart Relative to Biphasic Insulin Lispro and Biphasic Human Insulin in Patients With Type 2 Diabetes

Kjeld Hermansen, MD, DMSC, Michele Colombo, MD, Heidi Storgaard, MD, Anette Østergaard, MSC PHARM, Klaus Kølendorf, MD and Sten Madsbad, MD

University Department of Endocrinology and Metabolism, Aarhus Amtssygehus, Aarhus, Denmark

OBJECTIVE—The rapid-acting insulin analogs aspart and lispro have now been developed in biphasic formulations. This trial compared the postprandial serum glucose control of biphasic insulin aspart 30 (BIAsp 30: 30% aspart, 70% protaminated aspart) with that of biphasic insulin lispro 25 (Mix25: 25% lispro, 75% protaminated lispro) and biphasic human insulin 30 (BHI 30: 30% regular insulin, 70% NPH insulin) in insulin-treated subjects with type 2 diabetes.

RESEARCH DESIGN AND METHODS—This was an open-labeled, randomized, single-dose, three-way crossover trial of 61 insulin-treated subjects with type 2 diabetes who had no significant late diabetic complications. BIAsp 30 and Mix25 were injected subcutaneously immediately before a test meal, and BHI 30 was injected 15 min before a test meal. The primary target of analysis was serum glucose excursion 0–5 h after a meal.

RESULTS—The postprandial glycemic control with BIAsp 30, as assessed by the 5-h postmeal serum glucose excursion, was superior to that with both BHI 30 and Mix25 (16.6 ± 4.5 vs. 20.1 ± 4.9 and 18.9 ± 6.1 mmol/l per hour, respectively; P < 0.001 and P < 0.05). For BIAsp 30 versus BHI 30, this was supported by a reduced maximum glucose concentration [Cmax(SG)] (-5%; P < 0.05) occurring earlier (-13 min; P < 0.01). Furthermore, BIAsp 30 displayed a higher maximum serum insulin concentration (+101%; P < 0.001) occurring earlier (-55 min; P < 0.001) compared with BHI 30. Compared with Mix25, there was a shorter time to Cmax(SG) (-11 min; P < 0.05) after treatment with BIAsp 30.

CONCLUSIONS—This trial demonstrates that BIAsp 30 improves postprandial glycemic control compared with both Mix25 and BHI 30 in subjects with type 2 diabetes.

Abbreviations: AUC, area under the curve • BHI 30, biphasic human insulin 30 • BIAsp 30, biphasic insulin apart 30 • DCCT, Diabetes Control and Complications Trial • DECODE, Diabetes Epidemiology: Collaborative Analysis Of Diagnostic Criteria in Europe • IAsp, insulin aspart • Mix25, biphasic insulin lispro 25 • PP, per protocol


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