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Comparison of Vildagliptin and Pioglitazone in Korean Patients with Type 2 Diabetes Inadequately Controlled with Metformin

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dc.contributor.authorKim, Jong Ho-
dc.contributor.authorKim, Sang Soo-
dc.contributor.authorBaek, Hong Sun-
dc.contributor.authorLee, In Kyu-
dc.contributor.authorChung, Dong Jin-
dc.contributor.authorSohn, Ho Sang-
dc.contributor.authorBae, Hak Yeon-
dc.contributor.authorKim, Mi Kyung-
dc.contributor.authorPark, Jeong Hyun-
dc.contributor.authorChoi, Young Sik-
dc.contributor.authorKim, Young Il-
dc.contributor.authorHahm, Jong Ryeal-
dc.contributor.authorLee, Chang Won-
dc.contributor.authorJo, Sung Rae-
dc.contributor.authorPark, Mi Kyung-
dc.contributor.authorLee, Kwang Jae-
dc.contributor.authorKim, In Joo-
dc.date.accessioned2022-12-26T20:05:50Z-
dc.date.available2022-12-26T20:05:50Z-
dc.date.issued2016-06-
dc.identifier.issn2233-6079-
dc.identifier.issn2233-6087-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/15430-
dc.description.abstractBackground: We compared the efficacies of vildagliptin (50 mg twice daily) relative to pioglitazone (15 mg once daily) as an add-on treatment to metformin for reducing glycosylated hemoglobin (HbA1c) levels in Korean patients with type 2 diabetes. Methods: The present study was a multicenter, randomized, active-controlled investigation comparing the effects of vildagliptin and pioglitazone in Korean patients receiving a stable dose of metformin but exhibiting inadequate glycemic control. Each patient underwent a 16-week treatment period with either vildagliptin or pioglitazone as an add-on treatment to metformin. Results: The mean changes in HbA1c levels from baseline were -0.94% in the vildagliptin group and -0.6% in the pioglitazone group and the difference between the treatments was below the non-inferiority margin of 0.3%. The mean changes in postprandial plasma glucose (PPG) levels were -60.2 mg/dL in the vildagliptin group and -38.2 mg/dL in the pioglitazone group and these values significantly differed (P=0.040). There were significant decreases in the levels of total, low density lipoprotein, high density lipoprotein (HDL), and non-HDL cholesterol in the vildagliptin group but increases in the pioglitazone group. The mean change in body weight was -0.07 kg in the vildagliptin group and 0.69 kg in the pioglitazone group, which were also significantly different (P= 0.002). Conclusion: As an add-on to metformin, the efficacy of vildagliptin for the improvement of glycemic control is not inferior to that of pioglitazone in Korean patients with type 2 diabetes. In addition, add-on treatment with vildagliptin had beneficial effects on PPG levels, lipid profiles, and body weight compared to pioglitazone.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherKOREAN DIABETES ASSOC-
dc.titleComparison of Vildagliptin and Pioglitazone in Korean Patients with Type 2 Diabetes Inadequately Controlled with Metformin-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.4093/dmj.2016.40.3.230-
dc.identifier.scopusid2-s2.0-84977090730-
dc.identifier.wosid000388077700008-
dc.identifier.bibliographicCitationDIABETES & METABOLISM JOURNAL, v.40, no.3, pp 230 - 239-
dc.citation.titleDIABETES & METABOLISM JOURNAL-
dc.citation.volume40-
dc.citation.number3-
dc.citation.startPage230-
dc.citation.endPage239-
dc.type.docTypeArticle-
dc.identifier.kciidART002115302-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClassesci-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaEndocrinology & Metabolism-
dc.relation.journalWebOfScienceCategoryEndocrinology & Metabolism-
dc.subject.keywordPlusGLUCAGON-LIKE PEPTIDE-1-
dc.subject.keywordPlusINSULIN SENSITIVITY-
dc.subject.keywordPlusORAL METFORMIN-
dc.subject.keywordPlusDOUBLE-BLIND-
dc.subject.keywordPlusIV ACTIVITY-
dc.subject.keywordPlusMELLITUS-
dc.subject.keywordPlusJAPANESE-
dc.subject.keywordPlusTHIAZOLIDINEDIONES-
dc.subject.keywordPlusTOLERABILITY-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordAuthorDipeptidyl peptidase 4 inhibitor-
dc.subject.keywordAuthorMetformin-
dc.subject.keywordAuthorThiazolidinediones-
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