Effect of Dipeptidyl Peptidase-4 Inhibitor, Vildagliptin on Plasminogen Activator Inhibitor-1 in Patients With Diabetes Mellitus

被引:15
|
作者
Tani, Shigemasa [1 ,2 ]
Takahashi, Atsuhiko [1 ,2 ]
Nagao, Ken [2 ]
Hirayama, Atsushi [2 ]
机构
[1] Nihon Univ Hosp, Dept Hlth Planning Ctr, Tokyo, Japan
[2] Nihon Univ, Dept Med, Div Cardiol, Sch Med, Tokyo, Japan
来源
AMERICAN JOURNAL OF CARDIOLOGY | 2015年 / 115卷 / 04期
关键词
GLUCAGON-LIKE PEPTIDE-1; DENSITY-LIPOPROTEIN HETEROGENEITY; SOLUBILIZED MEMBRANES; RECEPTORS; TRIGLYCERIDES; ASSOCIATION; METABOLISM; TISSUE; GLP-1; AMIDE;
D O I
10.1016/j.amjcard.2014.11.044
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Dipeptidyl peptidase-4 (DPP-4) inhibitors may affect the serum levels of plasminogen activator inhibitor-1 (PAI-1) associated with triglyceride (TG) metabolism, which is a prognostic factor for cardiovascular disease, in diabetic patients. We conducted an 8-week, prospective, randomized study in which we assigned type 2 diabetic patients who were inadequately controlled with antidiabetic therapy. to the vildagliptin group (50 mg bid, n = 49) or the control group (n = 49). The primary efficacy parameter was the change in the serum level of PAL-1, and the secondary end point was the change in the serum levels of TG-rich lipoproteins. In the vildagliptin group, significant decrease of the serum PAI-1 level by 16.3% (p <0.0001) and significant decreases of the serum TG, remnant-like particle cholesterol, and apolipoprotein B levels by 12.1% (p = 0.002), 13.9% (p = 0.003), and 9.5% (p <0.0001), respectively, were observed. No such changes were observed in the control group. Multivariate regression analyses identified the absolute change from the baseline (Delta) of the PAI-1, but not that of the fasting blood glucose or hemoglobin A1c, as independent predictors of the Delta TG, Delta remnant-like particle cholesterol, and Delta apolipoprotein B. In conclusion, treatment of type 2 diabetes with vildagliptin might prevent the progression of atherosclerotic cardiovascular disease in diabetic patients by decreasing the serum PAI-1 levels and improving TG metabolism. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:454 / 460
页数:7
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