Abstract |
Glucagon-like peptide-1 receptor analogues/agonists (GLP-1RAs) are well established as effective adjuncts to lifestyle modification in the treatment of type 2 diabetes (T2D) as monotherapy or in combination with oral glucose-lowering drugs ± insulin. The six subcutaneous GLP-1RA formulations (i.e. twice-daily exenatide, once-daily liraglutide and lixisenatide, and once-weekly dulaglutide, exenatide and semaglutide) currently available in the EU and USA have many similarities, but also some unique features and properties. By stimulating GLP-1 receptors, GLP-1RAs increase insulin secretion and suppress glucagon release in a glucose-dependent manner, thereby improving clinical and patient-reported outcomes related to glycaemic control and weight. They also have been shown to reduce, or at least not increase, the risk of major cardiovascular outcomes. GLP-1RAs are generally well tolerated, with gastrointestinal and injection-site reactions being the most troublesome drug-related adverse events, and are associated with a very low intrinsic risk of hypoglycaemia. Treatment with GLP-1RAs should be customized to meet the clinical needs and personal preferences of the individual.
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Authors | Katherine A Lyseng-Williamson |
Journal | Clinical drug investigation
(Clin Drug Investig)
Vol. 39
Issue 8
Pg. 805-819
(Aug 2019)
ISSN: 1179-1918 [Electronic] New Zealand |
PMID | 31317516
(Publication Type: Journal Article, Review)
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Chemical References |
- Blood Glucose
- Glucagon-Like Peptide-1 Receptor
- Glycated Hemoglobin A
- Hypoglycemic Agents
- Insulin
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Topics |
- Administration, Oral
- Blood Glucose
(drug effects)
- Diabetes Mellitus, Type 2
(drug therapy)
- Glucagon-Like Peptide-1 Receptor
(agonists)
- Glycated Hemoglobin
(analysis)
- Humans
- Hypoglycemia
(chemically induced)
- Hypoglycemic Agents
(administration & dosage, therapeutic use)
- Injections, Subcutaneous
- Insulin
(therapeutic use)
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