 
         
         
         Abstract
         
         The efficacy and safety of the preprandial injection of insulin lispro was compared
            with the oral administration of glibenclamide in patients with early type 2 diabetes.
            In this open-label, multicenter study, 143 patients with a glucagon-stimulated increase
            in C-peptide of at least 0.4 nmol/L were randomized to receive preprandial insulin
            lispro (LP) or glibenclamide (GB) for 26 weeks. Seventy-five patients received LP
            (51 male/24 female; age 40 to 70 years, duration of diabetes 4.4 ± 2.9 years) and
            68 patients received GB (39 male/29 female; age 39 to 70 years; duration of diabetes
            4.3 ± 3.4 years). After 12 weeks, mean 90 minute blood glucose excursions were 0.9
            ± 1.0 mmol/L for LP and 1.8 ± 1.2 mmol/L for GB (p < 0.0001). After 24 weeks, mean
            blood glucose excursions were 1.0 ± 1.1 mmol/L for LP and 1.7 ± 1.2 mmol/L for GB
            (p = 0.002). Body weight decreased slightly from 87.2 ± 2.3 to 86.5 ± 12.2 kg in the
            LP group and increased from 84.1 ± 13.7 to 84.4 ± 13.3 kg in the GB group. LP versus
            GB induced changes from baseline to endpoint in fasting C-peptide (nmol/L), proinsulin
            and insulin levels (pmol/L) were - 0.2 ± 0.4 versus - 0.1 ± 0.6 (p = 0.04), - 11.2
            ± 26.0 versus - 1.1 ± 17.3 (p = 0.03), and - 27.8 ± 147.4 versus + 32.6 ± 286.2 (not
            significant), respectively. HbA1c at baseline was 7.5 ± 1.0 % for LP and 7.7 ± 1.2 % for GB and did not change significantly
            in either group during the investigation. No significant difference was observed between
            the groups with respect to hypoglycemic episodes. Treatment with LP improved postprandial
            blood glucose control more than GB without increasing body weight or hypoglycemic
            episodes. In addition, use of LP was associated with a decrease in fasting C-peptide
            and proinsulin levels, suggesting a potential down regulation of endogenous insulin
            production and improved proinsulin processing efficiency.
         
         
         
            
Key words
         
         
            Early diabetes type 2 - Insulin lispro - Glibenclamide - C-peptide - Proinsulin -
               HbA1c
               
          
      
    
   
      
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Priv. Doz. Dr. Thomas Forst
            Institute for Clinical Research and Development
            
            Parcusstraße 8
            
            55116 Mainz
            
            Germany
            
            Email: Thomasf@ikfe.de