Genetically engineered insulin analogs: diabetes in the new millenium.

Tight glucose control is essential to minimize complications in diabetic patients. However, the pharmacokinetic characteristics of the currently available rapid-, intermediate-, and long-acting preparations of human insulin make it almost impossible to achieve sustained normoglycemia. Until recently, improvements in insulin formulations were seriously limited as advances were only achieved in insulin purity, species, and characteristics of the retarding agent. The availability of molecular genetic techniques opened new windows to create insulin analogs by changing the structure of the native protein and to improve the therapeutic properties. The first clinically available insulin analog, Lispro, confirmed the hopes by showing that improved glycemic control can be achieved without an increase in hypoglycemic events. This requires, however, optimal basal insulin replacement, either by multiple daily injections of neutral protein Hagedorn (NPH) insulin or by insulin pump. Evidence suggests that short-acting insulin analogs would be better matched by a true basal insulin than by the erratically absorbed and rather short-acting NPH insulin. Therefore, future availability of long-acting analogs raises the hope to realize the true potential benefits of the currently available short-acting analog, Lispro, and of those still awaiting approval. The introduction of new short-acting and the first truly long-acting analogs, the development of analogs with increased stability, less variability and perhaps selective action will help to develop more individualized treatment strategies targeted to specific patient characteristics and to achieve further improvements in glycemic control.

[1]  S. Genuth,et al.  The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus. , 1993, The New England journal of medicine.

[2]  U. Ribel,et al.  Albumin binding of insulins acylated with fatty acids: characterization of the ligand-protein interaction and correlation between binding affinity and timing of the insulin effect in vivo. , 1995, The Biochemical journal.

[3]  L. Heinemann,et al.  Insulin Aspart in a 30/70 Premixed Formulation: Pharmacodynamic properties of a rapid-acting insulin analog in stable mixture , 1997, Diabetes Care.

[4]  B. Zinman,et al.  Insulin Lispro in CSII: Results of a Double-Blind Crossover Study , 1997, Diabetes.

[5]  S. Gammeltoft,et al.  Receptor Binding and Tyrosine Kinase Activation by Insulin Analogues With Extreme Affinities Studied in Human Hepatoma HepG2 Cells , 1991, Diabetes.

[6]  D. Brems,et al.  Improved insulin stability through amino acid substitution. , 1992, Protein engineering.

[7]  L. Vignati,et al.  Reduction of postprandial hyperglycemia and frequency of hypoglycemia in IDDM patients on insulin-analog treatment. Multicenter Insulin Lispro Study Group. , 1997 .

[8]  L. Heinemann,et al.  Do Insulin‐treated Diabetic Patients Use an Injection‐meal‐interval in Daily Life? , 1995, Diabetic medicine : a journal of the British Diabetic Association.

[9]  L. Heinemann,et al.  Variability of the metabolic effect of soluble insulin and the rapid-acting insulin analog insulin aspart. , 1998, Diabetes care.

[10]  L. Vignati,et al.  Reduction of Postprandial Hyperglycemia and Frequency of Hypoglycemia in IDDM Patients on Insulin-Analog Treatment , 1997, Diabetes.

[11]  H. Klein,et al.  Sustained signalling from the insulin receptor after stimulation with insulin analogues exhibiting increased mitogenic potency. , 1996, The Biochemical journal.

[12]  R. Landgraf,et al.  Use of insulin lispro in continuous subcutaneous insulin infusion treatment. Results of a multicenter trial. German Humalog-CSII Study Group. , 1999, Diabetes care.

[13]  Abstract , 1952 .

[14]  A. Vaag,et al.  NovoSol Basal: pharmacokinetics of a novel soluble long acting insulin analogue. , 1989, BMJ.

[15]  F. Shojaee-Moradie,et al.  Novel hepatoselective insulin analogues: studies with covalently linked thyroxyl‐insulin complexes , 1998, Diabetic medicine : a journal of the British Diabetic Association.

[16]  D. Howey,et al.  Biosynthetic Human Proinsulin: Review of Chemistry, in Vitro and in Vivo Receptor Binding, Animal and Human Pharmacology Studies, and Clinical Trial Experience , 1992, Diabetes Care.

[17]  M. Trautmann,et al.  Intensive insulin therapy with insulin lispro in patients with type 1 diabetes reduces the frequency of hypoglycemic episodes. , 2009, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

[18]  M. Trautmann,et al.  Severe insulin resistance treated with insulin lispro , 1996, The Lancet.

[19]  P. Brunetti,et al.  Use of the short‐acting insulin analogue lispro in intensive treatment of Type 1 diabetes mellitus: importance of appropriate replacement of basal insulin and time‐interval injection‐meal , 1998, Diabetic medicine : a journal of the British Diabetic Association.

[20]  P. Brunetti,et al.  Contribution of postprandial versus interprandial blood glucose to HbA1c in type 1 diabetes on physiologic intensive therapy with lispro insulin at mealtime. , 1999, Diabetes care.

[21]  O Faber,et al.  Insulin Pharmacokinetics , 1984, Diabetes Care.

[22]  Warszawski Uniwersytet Medyczny,et al.  Diabetes care , 2019, Health at a Glance.

[23]  M. Davidson,et al.  The Variability in the Action of Unmodified Insulin is More Dependent on Changes in Tissue Insulin Sensitivity than on Insulin Absorption , 1988, Diabetic medicine : a journal of the British Diabetic Association.

[24]  B. Zinman,et al.  Stability of Insulin Lispro in Insulin Infusion Systems , 1997, Diabetes Care.

[25]  M. Burge,et al.  Optimal administration of lispro insulin in hyperglycemic type 1 diabetes. , 1999, Diabetes care.

[26]  N. Fineberg,et al.  Immunologic Effects of Insulin Lispro [Lys (B28), Pro (B29) Human Insulin] in IDDM and NIDDM Patients Previously Treated With Insulin , 1996, Diabetes.

[27]  P. Home,et al.  Improved glycemic control with insulin aspart: a multicenter randomized double-blind crossover trial in type 1 diabetic patients. UK Insulin Aspart Study Group. , 1998, Diabetes care.

[28]  A. Lindholm,et al.  Improved postprandial glycemic control with insulin aspart. A randomized double-blind cross-over trial in type 1 diabetes. , 1999, Diabetes care.

[29]  S. R. Myers,et al.  Acylation of Human Insulin With Palmitic Acid Extends the Time Action of Human Insulin in Diabetic Dogs , 1997, Diabetes.

[30]  J. Rosenstock,et al.  Efficacy and Safety of HOE 901 (Insulin Glargine) in Subjects with Type 2 DM: A 28-Week Randomized, NPH Insulin-Controlled Trial , 1999 .

[31]  P. Brunetti,et al.  Long-term intensive treatment of type 1 diabetes with the short-acting insulin analog lispro in variable combination with NPH insulin at mealtime. , 1999, Diabetes care.

[32]  L. Slieker,et al.  Insulin and IGF-I analogs: novel approaches to improved insulin pharmacokinetics. , 1993, Advances in experimental medicine and biology.

[33]  H. Häring,et al.  The long acting human insulin analog HOE 901: characteristics of insulin signalling in comparison to Asp(B10) and regular insulin. , 1998, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

[34]  W. Duckworth,et al.  Differences in the cellular processing of AspB10 human insulin compared with human insulin and LysB28ProB29 human insulin. , 1999, Metabolism: clinical and experimental.

[35]  S. Havelund,et al.  Effect of fatty acids and selected drugs on the albumin binding of a long-acting, acylated insulin analogue. , 1997, Journal of pharmaceutical sciences.

[36]  Gareth R. Williams,et al.  Severe insulin resistance treated with insulin lispro , 1997, The Lancet.

[37]  H. Chase,et al.  Long‐term efficacy of Humalogã in subjects with Type 1 diabetes mellitus , 1999, Diabetic medicine : a journal of the British Diabetic Association.

[38]  K. Drejer The bioactivity of insulin analogues from in vitro receptor binding to in vivo glucose uptake. , 1992, Diabetes/metabolism reviews.

[39]  L. Vignati,et al.  Health-Related Quality-of-Life Results From Multinational Clinical Trials of Insulin Lispro: Assessing benefits of a new diabetes therapy , 1997, Diabetes Care.

[40]  M. Knip,et al.  Severe Antibody-Mediated Human Insulin Resistance: Successful Treatment With the Insulin Analog Lispro: A case report , 1997, Diabetes Care.

[41]  M. Trautmann,et al.  Improved postprandial blood glucose control and reduced nocturnal hypoglycemia during treatment with two novel insulin lispro-protamine formulations, insulin lispro mix25 and insulin lispro mix50. Mix50 Study Group. , 1999, Clinical therapeutics.

[42]  William V Tamborlane,et al.  Comparison of Human Regular and Lispro Insulins After Interruption of Continuous Subcutaneous Insulin Infusion and in the Treatment of Acutely Decompensated IDDM , 1998, Diabetes Care.

[43]  Y. Shechter,et al.  New concept for long-acting insulin: spontaneous conversion of an inactive modified insulin to the active hormone in circulation: 9-fluorenylmethoxycarbonyl derivative of insulin. , 1999, Diabetes.

[44]  P. Katsoyannis,et al.  A superactive insulin : [ B 10-Aspartic acid ] insulin ( human ) ( insulin analogue / peptide synthesis / biological activity ) , 2022 .

[45]  W. Duckworth Tumor necrosis factor and insulin resistance: specificity of sequence accounts of inhibition of insulin action. , 1997, The Journal of laboratory and clinical medicine.

[46]  Novel Hepatoselective Insulin Analog , 2001 .

[47]  D. Howey,et al.  [Lys(B28), Pro(B29)]-Human Insulin: A Rapidly Absorbed Analogue of Human Insulin , 1994, Diabetes.

[48]  M. Berger Towards more physiological insulin therapy in the 1990s. A comment. , 1989, Diabetes research and clinical practice.

[49]  D. Leroith,et al.  Current Directions in Insulin-Like Growth Factor Research , 2013, Advances in Experimental Medicine and Biology.

[50]  M. Lavelle-Jones,et al.  Selective suppression of hepatic glucose output by human proinsulin in the dog. , 1987, The American journal of physiology.

[51]  J. M. Beals,et al.  LYS(B28)PRO(B29)-HUMAN INSULIN , 1996 .

[52]  D. Cohen,et al.  Metabolically inactive insulin analog prevents type I diabetes in prediabetic NOD mice. , 1997, The Journal of clinical investigation.

[53]  D. Rogers,et al.  The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus , 1994 .

[54]  R. Heine,et al.  Nighttime Insulin Kinetics and Glycemic Control in Type 1 Diabetes Patients Following Administration of an Intermediate-Acting Lispro Preparation , 1997, Diabetes Care.

[55]  V. Koivisto,et al.  Meta-Analysis of the Effect of Insulin Lispro on Severe Hypoglycemia in Patients With Type 1 Diabetes , 1998, Diabetes Care.

[56]  L. Vignati,et al.  Basal activity profiles of NPH and [Nɛ-palmitoyl Lys (B29)] human insulins in subjects with IDDM , 1998, Diabetologia.

[57]  K. Polonsky,et al.  The Effects of Biosynthetic Human Proinsulin on Carbohydrate Metabolism , 1984, Diabetes.

[58]  J. Brange,et al.  Monomeric insulins obtained by protein engineering and their medical implications , 1988, Nature.

[59]  L. Heinemann,et al.  Time‐action profile of the soluble, fatty acid acylated, long‐acting insulin analogue NN304 , 1999, Diabetic medicine : a journal of the British Diabetic Association.

[60]  F. Matsuzaki,et al.  GROWTH-PROMOTING AND METABOLIC EFFECTS OF GROWTH HORMONE. , 1964, Metabolism: clinical and experimental.

[61]  G. Park,et al.  Long-acting insulin analogs. , 1999, Diabetes care.