From pumps to prevention: recent advances in the treatment of type 1 diabetes

Drug Discov Today. 2009 Oct;14(19-20):973-81. doi: 10.1016/j.drudis.2009.06.011. Epub 2009 Jul 4.

Abstract

Treatment options for pediatric patients living with type 1 diabetes mellitus (T1DM) have drastically changed over the past 30 years. Technological advances including the development of continuous subcutaneous insulin infusion (CSII) and continuous glucose monitoring (CGM) have allowed for improved insulin delivery and a better understanding of blood glucose fluctuations. Manipulations of CSII and CGM will allow for the development of an artificial pancreas; initial studies of this technology will be reviewed. New medications for the treatment of T1DM have been developed, such as rapid-acting insulins. Another area of exploration is the autoimmune process that causes beta-cell destruction. Immunomodulators used for T1DM prevention and secondary intervention will be reviewed.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Autoimmunity / drug effects
  • Biosensing Techniques
  • Blood Glucose / drug effects
  • Blood Glucose Self-Monitoring
  • Diabetes Mellitus, Type 1 / blood
  • Diabetes Mellitus, Type 1 / drug therapy*
  • Diabetes Mellitus, Type 1 / immunology
  • Diabetes Mellitus, Type 1 / prevention & control
  • Drug Therapy, Combination
  • Glycated Hemoglobin / metabolism
  • Humans
  • Hypoglycemic Agents / administration & dosage
  • Hypoglycemic Agents / pharmacokinetics
  • Hypoglycemic Agents / therapeutic use*
  • Immunologic Factors / therapeutic use*
  • Infusion Pumps
  • Insulin / administration & dosage
  • Insulin / analogs & derivatives
  • Insulin / pharmacokinetics
  • Insulin / therapeutic use
  • Insulin-Secreting Cells / drug effects*
  • Insulin-Secreting Cells / immunology
  • Insulin-Secreting Cells / metabolism
  • Pancreas, Artificial*
  • Primary Prevention
  • Treatment Outcome

Substances

  • Blood Glucose
  • Glycated Hemoglobin A
  • Hypoglycemic Agents
  • Immunologic Factors
  • Insulin
  • hemoglobin A1c protein, human