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Individualized, patient-centered use of lixisenatide for the treatment of type 2 diabetes mellitus
- Source :
- Expert Opinion on Drug Metabolism and Toxicology, Expert Opinion on Drug Metabolism and Toxicology, Taylor & Francis, 2017, 13 (3), pp.311-321. 〈10.1080/17425255.2017.1251579〉, Expert Opinion on Drug Metabolism and Toxicology, Taylor & Francis, 2017, 13 (3), pp.311-321. ⟨10.1080/17425255.2017.1251579⟩
- Publication Year :
- 2017
- Publisher :
- HAL CCSD, 2017.
-
Abstract
- International audience; Type 2 diabetes mellitus (T2DM) is a chronic metabolic disease associated with hyperglycemia, which can lead to serious vascular complications. Current treatment guidelines place particular emphasis on personalization of therapy. Within this guidance, the use of various second-line therapies, including glucagon-like peptide-1 receptor agonists (GLP-1 RAs), is recommended under certain circumstances. Areas covered: Factors influencing glucose homeostasis, including gastric emptying and the associated cardiovascular (CV) risk when homeostasis is not maintained, are reviewed. Physiology relating to the mechanism of action of GLP-1 RAs is summarized, with a particular focus on lixisenatide. In addition, an overview of efficacy and safety data for lixisenatide is presented and the CV effects of GLP-1 RAs are examined. Finally, the rationale and clinical data supporting the combination of lixisenatide and basal insulin are explored. Expert opinion: GLP-1 analogs meet a need for better glycemic control, with the added benefits of reduced hypoglycemic risk and body weight. The combination of a short-acting GLP-1 RA, such as lixisenatide, with a basal insulin, exploits the complementary effects of both of these therapies and seems well suited for the treatment of T2DM. However, further studies are needed to establish the associated CV risks and/or benefits of GLP-1 RAs.
- Subjects :
- Blood Glucose
cardiovascular risk
medicine.medical_specialty
type 2 diabetes mellitus
medicine.medical_treatment
Lixisenatide
030209 endocrinology & metabolism
[ SDV.BBM.BM ] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology
030204 cardiovascular system & hematology
Pharmacology
Toxicology
Glucagon-Like Peptide-1 Receptor
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
[ SDV.BBM.BC ] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Biomolecules [q-bio.BM]
Patient-Centered Care
medicine
individualized treatment
Animals
Humans
Hypoglycemic Agents
Insulin
Glucose homeostasis
postprandial plasma glucose
Precision Medicine
[SDV.BBM.BC]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Biochemistry [q-bio.BM]
Intensive care medicine
Gastric emptying
business.industry
Basal insulin
Type 2 Diabetes Mellitus
[SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology
General Medicine
Precision medicine
3. Good health
Diabetes Mellitus, Type 2
chemistry
Drug Therapy, Combination
Peptides
business
Patient centered
Subjects
Details
- Language :
- English
- ISSN :
- 17425255 and 17447607
- Database :
- OpenAIRE
- Journal :
- Expert Opinion on Drug Metabolism and Toxicology, Expert Opinion on Drug Metabolism and Toxicology, Taylor & Francis, 2017, 13 (3), pp.311-321. 〈10.1080/17425255.2017.1251579〉, Expert Opinion on Drug Metabolism and Toxicology, Taylor & Francis, 2017, 13 (3), pp.311-321. ⟨10.1080/17425255.2017.1251579⟩
- Accession number :
- edsair.doi.dedup.....df2dc21f63a422d256f302f58e02b676
- Full Text :
- https://doi.org/10.1080/17425255.2017.1251579〉