HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Efficacy and safety of incretin based therapies: clinical trial data.

AbstractOBJECTIVE:
Provide a comprehensive overview of efficacy and safety data on incretin-based agents in the treatment of type 2 diabetes.
DATA SOURCES:
A PubMed search was conducted for the years 2000-2009, using as keywords the names of glucagon-like peptide-1 (GLP-1) receptor agonists (exenatide and liraglutide) and dipeptidyl peptidase-4 (DPP-4) inhibitors (sitagliptin, alogliptin, and saxagliptin). World Diabetes Congress abstracts from 2008 to 2009 were also searched for clinical studies of these agents.
STUDY SELECTION:
The author included randomized controlled trials of incretin therapies that were published in English and enrolled > or =100 participants.
DATA EXTRACTION:
Data on the effects of incretins on glycemic control, weight, beta-cell function, blood pressure, lipid levels, safety, and tolerability were extracted and summarized.
DATA SYNTHESIS:
A total of 27 randomized controlled studies of incretin therapy were identified and included in the review. GLP-1 receptor agonists and DPP-4 inhibitors were evaluated at different points in the diabetes treatment spectrum, i.e., added to diet and exercise alone (monotherapy) or added to oral antihyperglycemic regimens (combination therapy).
CONCLUSION:
In addition to decreasing glycemia in type 2 diabetes, incretin therapies may improve other important parameters, including beta-cell function, blood pressure, and lipid levels, with a low risk for hypoglycemia. A comparison of the study data differentiates the clinical profiles of the GLP-1 receptor agonists, which are associated with weight loss, and DPP-4 inhibitors, which are weight neutral, as well as the individual agents within each class.
AuthorsJohn White
JournalJournal of the American Pharmacists Association : JAPhA (J Am Pharm Assoc (2003)) 2009 Sep-Oct Vol. 49 Suppl 1 Pg. S30-40 ISSN: 1544-3450 [Electronic] United States
PMID19801363 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
Chemical References
  • Blood Glucose
  • Dipeptidyl-Peptidase IV Inhibitors
  • GLP1R protein, human
  • Glucagon-Like Peptide-1 Receptor
  • Glycated Hemoglobin A
  • Hypoglycemic Agents
  • Incretins
  • Insulin
  • Lipids
  • Receptors, Glucagon
  • hemoglobin A1c protein, human
  • DPP4 protein, human
  • Dipeptidyl Peptidase 4
Topics
  • Blood Glucose (drug effects)
  • Blood Pressure (drug effects)
  • Diabetes Mellitus, Type 2 (drug therapy, metabolism)
  • Dipeptidyl Peptidase 4 (metabolism)
  • Dipeptidyl-Peptidase IV Inhibitors (administration & dosage, adverse effects, therapeutic use)
  • Drug Administration Schedule
  • Evidence-Based Medicine
  • Glucagon-Like Peptide-1 Receptor
  • Glycated Hemoglobin (metabolism)
  • Humans
  • Hypoglycemic Agents (administration & dosage, adverse effects, therapeutic use)
  • Incretins (metabolism)
  • Insulin (metabolism)
  • Insulin-Secreting Cells (drug effects, metabolism)
  • Lipids (blood)
  • Randomized Controlled Trials as Topic
  • Receptors, Glucagon (agonists, metabolism)
  • Treatment Outcome
  • Weight Loss (drug effects)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: