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Predictive clinical parameters for the therapeutic efficacy of sitagliptin in korean type 2 diabetes mellitus.

Authors :
Kim SA
Shim WH
Lee EH
Lee YM
Beom SH
Kim ES
Yoo JS
Nam JS
Cho MH
Park JS
Ahn CW
Kim KR
Source :
Diabetes & metabolism journal [Diabetes Metab J] 2011 Apr; Vol. 35 (2), pp. 159-65. Date of Electronic Publication: 2011 Apr 30.
Publication Year :
2011

Abstract

Background: Sitagliptin is a highly selective dipeptidyl peptide-4 (DPP-4) inhibitor that increases blood levels of active glucagon-like peptide (GLP)-1 and glucose-dependent insulinotrophic polypeptide (GIP), resulting in increased insulin secretion. While studies conducted in other countries have indicated the efficacy and safety of using sitagliptin to treat type 2 diabetes mellitus (T2DM), its predictors of effects to sitagliptin are not well understood. Therefore, we evaluated the predictive clinical parameters for the therapeutic benefits of sitagliptin when added to an ongoing metformin or sulfonylurea therapy in Korean T2DM subjects.<br />Methods: We obtained data from 251 Korean T2DM subjects who had recently started taking sitagliptin as add-on therapy. Exclusion criteria included any insulin use. Changes in HbA1c (ΔHbA1c) and fasting plasma glucose (ΔFPG) were assessed by comparing baseline levels prior to sitagliptin administration to levels 12 and 24 weeks after treatment. Responders were defined as subjects who experienced decrease from baseline of >10% in ΔHbA1c or >20% in ΔFPG levels at 24 weeks.<br />Results: We classified 81% of the subjects (204 out of 251) as responders. The responder group had a lower mean body mass index (23.70±2.40 vs. 26.00±2.26, P≤0.01) and were younger (58.83±11.57 years vs. 62.87±12.09 years, P=0.03) than the non-responder group.<br />Conclusion: In Korean T2DM subjects, sitagliptin responders had lower body mass index and were younger compared to non-responders.

Details

Language :
English
ISSN :
2233-6087
Volume :
35
Issue :
2
Database :
MEDLINE
Journal :
Diabetes & metabolism journal
Publication Type :
Academic Journal
Accession number :
21738898
Full Text :
https://doi.org/10.4093/dmj.2011.35.2.159