Pharmacology, efficacy and safety of liraglutide in the management of type 2 diabetes
Joshua J Neumiller1, Travis E Sonnett2, Lindy D Wood1, Stephen M Setter1, R Keith Campbell21Department of Pharmacotherapy, College of Pharmacy, Washington State University, Spokane, Washington; 2Department of Pharmacotherapy, College of Pharmacy, Washington State University, Pullman, Washington, USA...
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Dove Medical Press
2010
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oai:doaj.org-article:5e09cbf896884ef599e1aa2aec7e23ea2021-12-02T01:07:20ZPharmacology, efficacy and safety of liraglutide in the management of type 2 diabetes1178-7007https://doaj.org/article/5e09cbf896884ef599e1aa2aec7e23ea2010-07-01T00:00:00Zhttps://www.dovepress.com/pharmacology-efficacy-and-safety-of-liraglutide-in-the-management-of-t-peer-reviewed-article-DMSOhttps://doaj.org/toc/1178-7007Joshua J Neumiller1, Travis E Sonnett2, Lindy D Wood1, Stephen M Setter1, R Keith Campbell21Department of Pharmacotherapy, College of Pharmacy, Washington State University, Spokane, Washington; 2Department of Pharmacotherapy, College of Pharmacy, Washington State University, Pullman, Washington, USAAbstract: Liraglutide is a glucagon-like peptide-1 analog with pharmacokinetic properties suitable for once-daily administration approved by the Food and Drug Administration for the treatment of patients with type 2 diabetes. Clinical trial data from large, controlled studies ­demonstrate the safety and efficacy of liraglutide in terms of hemoglobin A1c (HbA1c) reduction, reductions in body weight, and the drug’s low risk for hypoglycemic events when used as monotherapy. ­Liraglutide has been studied as monotherapy and in combination with metformin, glimepiride, and ­rosiglitazone for the treatment of type 2 diabetes. Additionally, comparative data with insulin glargine and exenatide therapy are available from Phase III trials. Once-daily ­administration may provide a therapeutic advantage for liraglutide over twice-daily exenatide, with similar improvements in HbA1c and body weight observed when liraglutide was compared with exenatide. The glucose-dependent mechanism of insulin release with incretin analog therapy holds potential clinical significance in the management of postprandial hyperglycemic excursions, with minimal risk of hypoglycemia when used with non-secretagogue medications. Data to date on patient-reported outcomes with liraglutide treatment are encouraging. The most common adverse events associated with liraglutide therapy are dose-dependent nausea, vomiting, and diarrhea. Diligent postmarketing surveillance to elucidate the risk of pancreatitis and medullary thyroid carcinoma in a heterogeneous population are likely warranted.Keywords: incretin analog, incretin effect, liraglutide, diabetesCampbell RKNeumiller JDove Medical PressarticleKeywords: incretin analogincretin effectliraglutidevictozaSpecialties of internal medicineRC581-951ENDiabetes, Metabolic Syndrome and Obesity: Targets and Therapy, Vol Volume 3, Pp 215-226 (2010) |
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Keywords: incretin analog incretin effect liraglutide victoza Specialties of internal medicine RC581-951 |
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Keywords: incretin analog incretin effect liraglutide victoza Specialties of internal medicine RC581-951 Campbell RK Neumiller J Pharmacology, efficacy and safety of liraglutide in the management of type 2 diabetes |
| description |
Joshua J Neumiller1, Travis E Sonnett2, Lindy D Wood1, Stephen M Setter1, R Keith Campbell21Department of Pharmacotherapy, College of Pharmacy, Washington State University, Spokane, Washington; 2Department of Pharmacotherapy, College of Pharmacy, Washington State University, Pullman, Washington, USAAbstract: Liraglutide is a glucagon-like peptide-1 analog with pharmacokinetic properties suitable for once-daily administration approved by the Food and Drug Administration for the treatment of patients with type 2 diabetes. Clinical trial data from large, controlled studies ­demonstrate the safety and efficacy of liraglutide in terms of hemoglobin A1c (HbA1c) reduction, reductions in body weight, and the drug’s low risk for hypoglycemic events when used as monotherapy. ­Liraglutide has been studied as monotherapy and in combination with metformin, glimepiride, and ­rosiglitazone for the treatment of type 2 diabetes. Additionally, comparative data with insulin glargine and exenatide therapy are available from Phase III trials. Once-daily ­administration may provide a therapeutic advantage for liraglutide over twice-daily exenatide, with similar improvements in HbA1c and body weight observed when liraglutide was compared with exenatide. The glucose-dependent mechanism of insulin release with incretin analog therapy holds potential clinical significance in the management of postprandial hyperglycemic excursions, with minimal risk of hypoglycemia when used with non-secretagogue medications. Data to date on patient-reported outcomes with liraglutide treatment are encouraging. The most common adverse events associated with liraglutide therapy are dose-dependent nausea, vomiting, and diarrhea. Diligent postmarketing surveillance to elucidate the risk of pancreatitis and medullary thyroid carcinoma in a heterogeneous population are likely warranted.Keywords: incretin analog, incretin effect, liraglutide, diabetes |
| format |
article |
| author |
Campbell RK Neumiller J |
| author_facet |
Campbell RK Neumiller J |
| author_sort |
Campbell RK |
| title |
Pharmacology, efficacy and safety of liraglutide in the management of type 2 diabetes |
| title_short |
Pharmacology, efficacy and safety of liraglutide in the management of type 2 diabetes |
| title_full |
Pharmacology, efficacy and safety of liraglutide in the management of type 2 diabetes |
| title_fullStr |
Pharmacology, efficacy and safety of liraglutide in the management of type 2 diabetes |
| title_full_unstemmed |
Pharmacology, efficacy and safety of liraglutide in the management of type 2 diabetes |
| title_sort |
pharmacology, efficacy and safety of liraglutide in the management of type 2 diabetes |
| publisher |
Dove Medical Press |
| publishDate |
2010 |
| url |
https://doaj.org/article/5e09cbf896884ef599e1aa2aec7e23ea |
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AT campbellrk pharmacologyefficacyandsafetyofliraglutideinthemanagementoftype2diabetes AT neumillerj pharmacologyefficacyandsafetyofliraglutideinthemanagementoftype2diabetes |
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