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Cited 13 time in webofscience Cited 10 time in scopus
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Comparison of Vildagliptin and Pioglitazone in Korean Patients with Type 2 Diabetes Inadequately Controlled with Metforminopen access

Authors
Kim, Jong HoKim, Sang SooBaek, Hong SunLee, In KyuChung, Dong JinSohn, Ho SangBae, Hak YeonKim, Mi KyungPark, Jeong HyunChoi, Young SikKim, Young IlHahm, Jong RyealLee, Chang WonJo, Sung RaePark, Mi KyungLee, Kwang JaeKim, In Joo
Issue Date
Jun-2016
Publisher
KOREAN DIABETES ASSOC
Keywords
Dipeptidyl peptidase 4 inhibitor; Metformin; Thiazolidinediones
Citation
DIABETES & METABOLISM JOURNAL, v.40, no.3, pp 230 - 239
Pages
10
Indexed
SCOPUS
ESCI
KCI
Journal Title
DIABETES & METABOLISM JOURNAL
Volume
40
Number
3
Start Page
230
End Page
239
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/15430
DOI
10.4093/dmj.2016.40.3.230
ISSN
2233-6079
2233-6087
Abstract
Background: 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.
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