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GLP-1 receptor agonists in diabetic kidney disease: current evidence and future directions

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dc.contributor.authorYu, Ji Hee-
dc.contributor.authorPark, So Young-
dc.contributor.authorLee, Da Young-
dc.contributor.authorKim, Nan Hee-
dc.contributor.authorSeo, Ji A.-
dc.date.accessioned2022-06-11T02:40:19Z-
dc.date.available2022-06-11T02:40:19Z-
dc.date.created2022-06-09-
dc.date.issued2022-03-
dc.identifier.issn2211-9132-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/141926-
dc.description.abstractWith the emergence of various classes of blood glucose-lowering agents, choosing the appropriate drug for each patient is empha-sized in diabetes management. Among incretin-based drugs, glucagon-like peptide 1 (GLP-1) receptor agonists are a promising thera-peutic option for patients with diabetic kidney disease (DKD). Several cardiovascular outcome trials have demonstrated that GLP-1 receptor agonists have beneficial effects on cardiorenal outcomes beyond their blood glucose-lowering effects in patients with type 2 diabetes mellitus (T2DM). The renal protective effects of GLP-1 receptor agonists likely result from their direct actions on the kidney, in addition to their indirect actions that improve conventional risk factors for DKD, such as reducing blood glucose levels, blood pres-sure, and body weight. Inhibition of oxidative stress and inflammation and induction of natriuresis are major renoprotective mecha-nisms of GLP-1 analogues. Early evidence from the development of dual and triple combination agents suggests that GLP-1 receptor agonists will probably become popular treatment options for patients with T2DM.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherKOREAN SOC NEPHROLOGY-
dc.subjectGLUCAGON-LIKE PEPTIDE-1-
dc.subjectDEPENDENT INSULINOTROPIC POLYPEPTIDE-
dc.subjectGASTRIC-INHIBITORY POLYPEPTIDE-
dc.subjectBROWN ADIPOSE-TISSUE-
dc.subjectCARDIOVASCULAR OUTCOMES-
dc.subjectFOOD-INTAKE-
dc.subjectCOMBINATION THERAPY-
dc.subjectHEPATIC STEATOSIS-
dc.subjectOXIDATIVE STRESS-
dc.subjectIN-VITRO-
dc.titleGLP-1 receptor agonists in diabetic kidney disease: current evidence and future directions-
dc.typeArticle-
dc.contributor.affiliatedAuthorYu, Ji Hee-
dc.identifier.doi10.23876/j.krcp.22.001-
dc.identifier.scopusid2-s2.0-85127918075-
dc.identifier.wosid000778371500002-
dc.identifier.bibliographicCitationKIDNEY RESEARCH AND CLINICAL PRACTICE, v.41, no.2, pp.136 - 149-
dc.relation.isPartOfKIDNEY RESEARCH AND CLINICAL PRACTICE-
dc.citation.titleKIDNEY RESEARCH AND CLINICAL PRACTICE-
dc.citation.volume41-
dc.citation.number2-
dc.citation.startPage136-
dc.citation.endPage149-
dc.type.rimsART-
dc.type.docTypeReview-
dc.identifier.kciidART002828722-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaUrology & Nephrology-
dc.relation.journalWebOfScienceCategoryUrology & Nephrology-
dc.subject.keywordPlusGLUCAGON-LIKE PEPTIDE-1-
dc.subject.keywordPlusDEPENDENT INSULINOTROPIC POLYPEPTIDE-
dc.subject.keywordPlusGASTRIC-INHIBITORY POLYPEPTIDE-
dc.subject.keywordPlusBROWN ADIPOSE-TISSUE-
dc.subject.keywordPlusCARDIOVASCULAR OUTCOMES-
dc.subject.keywordPlusFOOD-INTAKE-
dc.subject.keywordPlusCOMBINATION THERAPY-
dc.subject.keywordPlusHEPATIC STEATOSIS-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordAuthorDiabetic nephropathies-
dc.subject.keywordAuthorGlucagon-like peptide 1-
dc.subject.keywordAuthorType 2 diabetes mellitus-
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