Diabetes Research and Clinical Practice
Volume 62, Issue 3 , Pages 187-195, December 2003

Therapy after single oral agent failure: adding a second oral agent or an insulin mixture?

  • James K. Malone

      Affiliations

    • Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA
    • Corresponding Author InformationCorresponding author. Tel.: +1-317-277-6472; fax: +1-317-277-5458
  • ,
  • Scott D. Beattie

      Affiliations

    • Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA
  • ,
  • Barbara N. Campaigne

      Affiliations

    • Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA
  • ,
  • Patricia A. Johnson

      Affiliations

    • Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA
  • ,
  • Andrew S. Howard

      Affiliations

    • Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA
  • ,
  • Zvonko Milicevic

      Affiliations

    • Eli Lilly and Company, Regional Operations GES, M.B.H., Vienna, Austria

Received 2 May 2002; received in revised form 19 June 2003; accepted 4 August 2003.

Abstract 

Aim: to compare the glycemic response to an insulin lispro mixture (25% insulin lispro and 75% NPL) twice daily plus metformin (Mix25+M) with glibenclamide plus metformin (G+M), in patients with type 2 diabetes inadequately controlled with a single oral agent. Methods: 597 patients treated in a randomized, open-label, 16-week parallel study. Variables evaluated: hemoglobin A1C (A1C), patient symptoms, hypoglycemia rate (episodes/patient/30 days), and incidence (% patients experiencing ≥1 episode). For a subset of patients (N=120), fasting, 1-h, and 2-h postprandial plasma glucose (FPG, 1-h ppPG, 2-h ppPG) in response to a standardized test meal (STM) and self-monitored blood glucose (BG) profiles were measured. Results: improved A1C at endpoint for both groups, and A1C changes from baseline to endpoint were not significantly different between treatments (Mix25+M, −1.87±1.35% vs. G+M, −1.98±1.28%; p=0.288). Among patients completing STM; endpoint 2-h ppPG was significantly lower with Mix25+M (9.05±3.32 mmol/l vs. 12.31±3.65 mmol/l; p<0.001), as was 2-h ppPG excursion (2-h ppPGex)(0.38±3.23 mmol/l vs. 2.88±1.98 mmol/l; p<0.001). Percentage of patients achieving postprandial BG targets (<10 mmol/l) at endpoint was significantly greater with Mix25+M (80% vs. 48%; p<0.001). Although, overall hypoglycemia rates were similar, percentage of patients experiencing and rate of nocturnal hypoglycemia was less with Mix25+M (1% vs. 5%; p<0.01, and 0.01 vs. 0.08 episodes/pt/30 d; p=0.007). Patients reported less polyuria with Mix25+M (p<0.001). Conclusion: in patients with type 2 diabetes failing on metformin or a sulfonylurea, Mix25+M provided similar overall glycemic control, lower ppPG, reduced nocturnal hypoglycemia, and fewer hyperglycemic symptoms compared to G+M.

Keywords: Type 2 diabetes, Oral agents, Insulin mixtures

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PII: S0168-8227(03)00181-5

doi:10.1016/j.diabres.2003.08.003

Diabetes Research and Clinical Practice
Volume 62, Issue 3 , Pages 187-195, December 2003