Please use this identifier to cite or link to this item:
http://hdl.handle.net/10553/49722
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Gómez-Huelgas, Ricardo | en_US |
dc.contributor.author | Azriel, Sharona | en_US |
dc.contributor.author | Puig-Domingo, Manel | en_US |
dc.contributor.author | Vidal, Josep | en_US |
dc.contributor.author | De Pablos-Velasco, Pedro | en_US |
dc.date.accessioned | 2018-11-24T10:10:49Z | - |
dc.date.available | 2018-11-24T10:10:49Z | - |
dc.date.issued | 2015 | en_US |
dc.identifier.issn | 0946-1965 | en_US |
dc.identifier.uri | http://hdl.handle.net/10553/49722 | - |
dc.description.abstract | Despite the variety of therapeutic options for the management of type 2 diabetes mellitus, many patients fail to meet glycated hemoglobin (HbA1c) targets. The relative contribution of postprandial plasma glucose (PPG) to overall HbA1c is estimated at 40-60%, with the effect of PPG on HbA1c being prominent in patients on basal insulin. The development of glucagon-like peptide-1 receptor agonists (GLP-1RAs) has been an important achievement in diabetes management and has become an established treatment. Of available GLP-1RAs, lixisenatide is a once-daily prandial GLP-1RA that has been shown to produce a reduction in HbA1c with a pronounced postprandial effect, suggesting a complementary effect between lixisenatide and basal insulin on PPG and fasting plasma glucose, resulting in a beneficial effect on body weight in all populations. Therefore, lixisenatide will make an important addition to current options for treating diabetes, especially for patients not achieving glycemic targets with basal insulin therapy. | en_US |
dc.language | eng | en_US |
dc.relation.ispartof | International Journal of Clinical Pharmacology and Therapeutics | en_US |
dc.source | International Journal of Clinical Pharmacology and Therapeutics[ISSN 0946-1965],v. 53(3), p. 230-240 (Marzo 2015) | en_US |
dc.subject | 32 Ciencias médicas | en_US |
dc.subject | 3209 Farmacología | en_US |
dc.subject.other | Diabetes mellitus | en_US |
dc.subject.other | Glucagon | en_US |
dc.subject.other | Peptides | en_US |
dc.title | Glucagon-like peptide-1 receptor agonists as insulin add-on therapy in patients with inadequate glycemic control in type 2 diabetes mellitus: Lixisenatide as a new therapeutic option | en_US |
dc.type | info:eu-repo/semantics/review | en_US |
dc.type | Review | en_US |
dc.identifier.doi | 10.5414/CP202052 | en_US |
dc.identifier.scopus | 84938510015 | - |
dc.contributor.authorscopusid | 7004734060 | - |
dc.contributor.authorscopusid | 6603263764 | - |
dc.contributor.authorscopusid | 7004112528 | - |
dc.contributor.authorscopusid | 35430483700 | - |
dc.contributor.authorscopusid | 6603805479 | - |
dc.description.lastpage | 240 | en_US |
dc.description.firstpage | 230 | en_US |
dc.relation.volume | 53 | en_US |
dc.investigacion | Ciencias de la Salud | en_US |
dc.type2 | Reseña | en_US |
dc.description.numberofpages | 11 | en_US |
dc.utils.revision | Sí | en_US |
dc.date.coverdate | Marzo 2015 | en_US |
dc.identifier.ulpgc | Sí | en_US |
dc.identifier.ulpgc | Sí | en_US |
dc.identifier.ulpgc | Sí | en_US |
dc.identifier.ulpgc | Sí | en_US |
dc.contributor.buulpgc | BU-MED | en_US |
dc.description.sjr | 0,418 | - |
dc.description.jcr | 1,129 | - |
dc.description.sjrq | Q1 | - |
dc.description.jcrq | Q4 | - |
dc.description.scie | SCIE | - |
item.grantfulltext | none | - |
item.fulltext | Sin texto completo | - |
crisitem.author.dept | GIR IUIBS: Rendimiento humano, ejercicio físico y salud | - |
crisitem.author.dept | IU de Investigaciones Biomédicas y Sanitarias | - |
crisitem.author.dept | Departamento de Ciencias Médicas y Quirúrgicas | - |
crisitem.author.orcid | 0000-0002-9190-2581 | - |
crisitem.author.parentorg | IU de Investigaciones Biomédicas y Sanitarias | - |
crisitem.author.fullName | De Pablos Velasco, Pedro Luis | - |
Appears in Collections: | Reseña |
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