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Circadian profiles of blood glucose and plasma free insulin during treatment with Semisynthetic and Biosynthetic human insulin, and comparison with conventional monocomponent preparations

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Summary

Sixteen hospitalized insulin requiring diabetics treated with a single daily subcutaneous injection were randomly allocated either to a mixture of porcine Actrapid+Lente MC or a mixture of Regular+NPH—Biosynthetic human insulin (Study 1). In Study 2, 10 patients receiving two daily insulin injections were treated at random with either porcine Actrapid+Monotard, or Actrapid+Monotard—Semisynthetic human insulin or Regular+NPH—Biosynthetic human insulin. Once an optimal insulin regimen was obtained, circadian blood glucose and plasma free insulin profiles (7–9 time points) were determined with the two (Study 1) or three (Study 2) insulin preparations, keeping the doses of insulin constant. In Study 1 no significant difference in blood glucose (BG) or plasma free insulin (FIRI) profiles was observed. The mean daily blood glucose, the mean amplitude of glycaemic excursions (MAGE), the index of blood glucose control (M-value of Schlichtkrull), as well as the post-breakfast increases in blood glucose and mean free IRI, were similar with both types of insulin. In Study 2, BG and FIRI profiles were also similar, except for a significantly lower (p<0.02) BG at 8.30 p.m. with both human insulins. No significant differences were found in free IRI at that time. Mean BG, M index, MAGE and mean FIRI were similar but the postbreakfast increase was significantly smaller with SHI. In conclusion, the pharmacokinetics of animal monocomponent, semisynthetic and biosynthetic human insulin appear similar, but evening BG control was better with both types of human insulins given twice daily.

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References

  1. Markusen J, Damgaard U, Pingel M, Snel L, Sørensen AR, Sørensen E (1983) Human insulin (Novo): chemistry and characteristics. Diabetes Care [Suppl 1]: 4–8

  2. Chance RE, Kroeff EP, Hoffmann IA, Frank BH (1981) Chemical, physical and biologic properties of biosynthetic human insulin. Diabetes Care 4: 147–154

    Google Scholar 

  3. Owens DR, Jones MK, Hayes TM, Heding LG, Alberti KGMM, Homer PD, Burrin JM, Newcombe RG (1981) Human insulin: study of safety and efficacy in man. Br Med J 282: 1264–1266

    Google Scholar 

  4. Keen H, Glynne A, Pickup JC, Viberti GC, Bilous RW, Jarrett RJ, Marsden R (1980) Human insulin produced by recombinant DNA technology: safety and hypoglycaemic potency in healthy men. Lancet 2: 398–401

    Google Scholar 

  5. Nakagawa S, Nakayama H, Sasaki T, Yoshimo K, Yu Y, Shimoza KI, Aoki S, Mashima K (1973) Simple method for the determination of serum free insulin levels in insulin treated patients. Diabetes 22: 590–600

    Google Scholar 

  6. Heding LG (1975) Radioimmunological determination of human C-peptide in serum. Diabetologia 11: 541–548

    Google Scholar 

  7. Christiansen AH (1973) Radioimmunoelectroforesis in the determination of insulin binding to IgG. Methodological studies. Horm Metab Res 5: 147–154

    Google Scholar 

  8. Schoos R, Schoos-Barbette S, Lambotte C (1978) Dosage of hemoglobin A1c by isoelectrofocusing. Clin Chim Acta 86: 61–65

    Google Scholar 

  9. Schlichtkrull J, Munck O, Jersild M (1965) The M-value, an index of blood sugar control in diabetes. Acta Med Scand 177: 95–102

    Google Scholar 

  10. Service FJ, Molnar GD, Rosevear JW, Ackermann E, Gatewood LC, Taylor WF (1970) Mean amplitude of glycaemic excursions, a measure of diabetic instability. Diabetes 19: 644–655

    Google Scholar 

  11. Skyler JS (1982) Human insulin of recombinant DNA origin: clinical potential. Diabetes Care 5 [Suppl 2]: 181–186

    Google Scholar 

  12. Pickup JC, Bilous RW, Viberti GC, Keen H, Jarrett RJ, Glynne A, Cauldwell J, Root M, Rubenstein AH (1982) Plasma insulin and C-peptide after subcutaneous and intravenous administration of human insulin (recombinant DNA) and purified porcine insulin in healthy men. Diabetes Care 5 [Suppl 2]: 29–34

    Google Scholar 

  13. Kemmer FW, Sonnenberg G, Cuppers HJ, Berger M (1982) Absorption kinetics of semisynthetic human insulin and biosynthetic (recombinant DNA) human insulin. Diabetes Care 5 [Suppl 2]: 23–28

    Google Scholar 

  14. Botterman P, Gyaran H, Wahl K, Ermler R, Lebender A (1982) Insulin concentrations and time-action profiles of three different intermediate-acting insulin preparations in non diabetic volunteers under glucose-controlled glucose infusion technique. Diabetes Care 5 [Suppl 2]: 43–52

    Google Scholar 

  15. Colagiuri S, Kotowicz MA, Steinbeck AW, Kidson W (1983) Metabolic profiles in diabetic subjects treated with human insulin (Novo) and porcine insulin. Diabetes Care 6 [Suppl 1]: 49–52

    Google Scholar 

  16. Turner RC, Philips M, Jones R, Dornan IL, Holmes RR (1982) Ultralente-based insulin regimens in insulin dependent diabetics. In: Skyler JS (ed) Insulin update 1982. Excerpta Medica, Princeton, pp 157–174

    Google Scholar 

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Castillo, M., Nemery, A., Verdin, E. et al. Circadian profiles of blood glucose and plasma free insulin during treatment with Semisynthetic and Biosynthetic human insulin, and comparison with conventional monocomponent preparations. Eur J Clin Pharmacol 25, 767–771 (1983). https://doi.org/10.1007/BF00542517

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  • DOI: https://doi.org/10.1007/BF00542517

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