Inhaled insulin using the AERx Insulin Diabetes Management System in healthy and asthmatic subjects.

OBJECTIVE The AERx insulin Diabetes Management System (AERx iDMS) (Aradigm, Hayward, CA) delivers an aerosol of liquid human insulin to the deep lung for systemic absorption. This study examined the effects on pulmonary function, pharmacokinetics, and pharmacodynamics of inhaled insulin in asthmatic and nonasthmatic subjects without diabetes. RESEARCH DESIGN AND METHODS A total of 28 healthy and 17 asthmatic (forced expiratory volume during the first second [ FEV(1)] 50-80% of predicted value) subjects were enrolled in a two-part, open-label trial. To assess insulin pharmacokinetics and pharmacodynamics, a single inhalation dose of 1.57 mg (45 IU) was given on each of the 2 dosing days in part 1. A dose of 4.7 mg (135 IU) of insulin was inhaled in part 2 to assess effects on pulmonary function. RESULTS Inhaled insulin showed area under the curve (AUC)((0-360 min)) values that were significantly greater for healthy subjects than for asthmatic subjects (P = 0.013), whereas no difference was observed for maximum concentration (C(max)) in the two groups. A greater reduction of serum glucose as indicated by area over the curve (AOC)((0-360 min)) was observed in healthy subjects (P = 0.007). Asthmatic subjects had greater intrasubject variations in insulin AUC((0-360 min)) and C(max) values than healthy subjects, but similar variations in glucose AOC((0-360 min)). No significant changes in FEV(1), forced vital capacity (FVC), and FEV(1)/FVC were observed from pre- to postdose times, and there were no observed safety issues. CONCLUSIONS After inhaling insulin using the AERx iDMS, asthmatic subjects absorbed less insulin than healthy subjects, resulting in less reduction of serum glucose. No effects on airway reactivity were observed. Diabetic patients with asthma may need to inhale more insulin than patients with normal respiratory function in order to achieve similar glycemic control.

[1]  S. Mudaliar,et al.  Insulin aspart (B28 asp-insulin): a fast-acting analog of human insulin: absorption kinetics and action profile compared with regular human insulin in healthy nondiabetic subjects. , 1999, Diabetes care.

[2]  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.

[3]  I. Gonda,et al.  Design and testing of aerosol delivery systems for reproducible clinical performance. , 1998, Journal of aerosol medicine : the official journal of the International Society for Aerosols in Medicine.

[4]  A. McElduff,et al.  Pulmonary insulin administration using the AERx system: physiological and physicochemical factors influencing insulin effectiveness in healthy fasting subjects. , 2000, Diabetes technology & therapeutics.

[5]  R J Roberts,et al.  Human insulin. , 1984, Iowa medicine : journal of the Iowa Medical Society.

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

[7]  R. Turner,et al.  Homeostasis model assessment: insulin resistance and β-cell function from fasting plasma glucose and insulin concentrations in man , 1985, Diabetologia.

[8]  L. Heinemann,et al.  Time–action Profile of Inhaled Insulin , 1997, Diabetic medicine : a journal of the British Diabetic Association.

[9]  P. Wollmer,et al.  Quantitative evaluation of aerosol deposition pattern in the lung in patients with chronic bronchitis. , 1994, Physiological measurement.

[10]  John L. Hankinson,et al.  Standardization of Spirometry, 1994 Update. American Thoracic Society. , 1995, American journal of respiratory and critical care medicine.

[11]  D. Owens,et al.  Human Insulin: Clinical Pharmacological Studies in Normal Man , 1986 .

[12]  R M Gardner,et al.  Reference spirometric values using techniques and equipment that meet ATS recommendations. , 2015, The American review of respiratory disease.

[13]  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 .

[14]  R. Holman,et al.  Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33). UK Prospective Diabetes Study (UKPDS) Group. , 1998 .

[15]  T. Isawa,et al.  Effect of bronchodilation on the deposition and clearance of radioaerosol in bronchial asthma in remission. , 1987, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[16]  S J Farr,et al.  Inhalation delivery systems with compliance and disease management capabilities. , 1998, Journal of controlled release : official journal of the Controlled Release Society.

[17]  W. Bria,et al.  Hemodynamic, cardiac, and electrolyte effects of low-dose aerosolized terbutaline sulfate in asthmatic patients. , 1998, Chest.

[18]  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.

[19]  Uk-Prospective-Diabetes-Study-Group Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33) , 1998, The Lancet.

[20]  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.

[21]  A. Lindholm,et al.  Clinical Pharmacokinetics and Pharmacodynamics of Insulin Aspart , 2001, Clinical pharmacokinetics.

[22]  W. Cefalu,et al.  Inhaled Human Insulin Treatment in Patients with Type 2 Diabetes Mellitus , 2001, Annals of Internal Medicine.

[23]  E. Daviskas,et al.  Deposition of aqueous aerosol of technetium-99m diethylene triamine penta-acetic acid generated and delivered by a novel system (AERx) in healthy subjects , 1999, European Journal of Nuclear Medicine.

[24]  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.

[25]  W. Cefalu,et al.  Efficacy of inhaled human insulin in type 1 diabetes mellitus: a randomised proof-of-concept study , 2001, The Lancet.

[26]  G. Bolli,et al.  Insulin analogues and their potential in the management of diabetes mellitus , 1999, Diabetologia.

[27]  R. Blouin,et al.  In Vivo and In Vitro β2‐Adrenergic Receptor Responsiveness in Young and Elderly Asthmatics , 1992, Pharmacotherapy.

[28]  Jeff Schuster,et al.  The AERX™ Aerosol Delivery System , 1997, Pharmaceutical Research.

[29]  M. Ellmerer,et al.  Dose-response relation of liquid aerosol inhaled insulin in Type I diabetic patients , 2001, Diabetologia.

[30]  R. Ahrens,et al.  Albuterol: An Adrenergic Agent for Use in the Treatment of Asthma Pharmacology, Pharmacokinetics and Clinical Use , 1984, Pharmacotherapy.

[31]  D. Howey,et al.  Comparative Pharmacokinetics and Glucodynamics of Two Human Insulin Mixtures 70/30 and 50/50 insulin mixtures , 1994, Diabetes Care.