The effects of vildagliptin compared with metformin on vascular endothelial function and metabolic parameters: a randomized, controlled trial (Sapporo Athero-Incretin Study 3)

被引:29
作者
Kitao, Naoyuki [1 ]
Miyoshi, Hideaki [1 ]
Furumoto, Tomoo [2 ,3 ]
Ono, Kota [4 ]
Nomoto, Hiroshi [1 ]
Miya, Aika [1 ]
Yamamoto, Chiho [1 ]
Inoue, Atsushi [5 ]
Tsuchida, Kenichi [6 ]
Manda, Naoki [6 ]
Kurihara, Yoshio [7 ]
Aoki, Shin [8 ]
Nakamura, Akinobu [1 ]
Atsumi, Tatsuya [1 ]
机构
[1] Hokkaido Univ, Grad Sch Med, Div Rheumatol Endocrinol & Nephrol, Kita Ku, Kita-15 Nishi-7, Sapporo, Hokkaido 0608638, Japan
[2] Sapporo Hosp, NTT East Japan, Dept Cardiovasc Med, Sapporo, Hokkaido, Japan
[3] Hokkaido Univ, Grad Sch Med, Dept Cardiovasc Med, Sapporo, Hokkaido, Japan
[4] Hokkaido Univ Hosp, Clin Res & Med Innovat Ctr, Sapporo, Hokkaido, Japan
[5] Hokkaido Hosp, Japan Community Healthcare & Org, Sapporo, Hokkaido, Japan
[6] Manda Mem Hosp, Sapporo, Hokkaido, Japan
[7] Kurihara Clin, Sapporo, Hokkaido, Japan
[8] Aoki Clin, Sapporo, Hokkaido, Japan
来源
CARDIOVASCULAR DIABETOLOGY | 2017年 / 16卷
关键词
Type; 2; diabetes; Dipeptidyl peptidase-4 inhibitor; Vildagliptin; Vascular endothelial function; DIPEPTIDYL PEPTIDASE-4 INHIBITOR; TYPE-2; DIABETES-MELLITUS; CORONARY-HEART-DISEASE; FLOW-MEDIATED VASODILATION; GLUCAGON-LIKE PEPTIDE-1; APOLIPOPROTEIN-A-I; CARDIOVASCULAR OUTCOMES; MYOCARDIAL-INFARCTION; NONDIABETIC SUBJECTS; ARTERY-DISEASE;
D O I
10.1186/s12933-017-0607-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Dipeptidyl peptidase-4 (DPP-4) inhibitors may have protective effects in the early stage of atherosclerosis in patients with type 2 diabetes, although similar effects in advanced atherosclerosis were not shown in recent randomized placebo-controlled studies. Therefore, we investigated the efficacy of DPP-4 inhibitor on endothelial function and glycemic metabolism compared with high-dose metformin. Methods: In this multicenter, open-labeled, prospective, randomized, parallel-group comparison study, patients with type 2 diabetes treated with low-dose metformin (500-750 mg/day) were enrolled and randomly assigned to a vildagliptin, a DPP-4 inhibitor, add-on group (Vilda) or a double dose of metformin group (high Met) for 12 weeks. Flow-mediated dilation (FMD) and serum metabolic markers were assessed before and after treatment. In addition, glycemic control and metabolic parameters were also assessed. Results: Ninety-seven subjects (aged 58.7 +/- 11.0 years; body mass index, 25.9 +/- 4.4 kg/m(2); HbA1c, 7.3 +/- 0.5%; FMD, 5.8 +/- 2.6%) were enrolled. Eight subjects dropped out by the end of the study. There were no significant differences between the two groups in baseline characteristics. After 12 weeks, HbA1c was significantly improved in the Vilda group compared with the high Met group (-0.80 +/- 0.38% vs. -0.40 +/- 0.47%, respectively; p < 0.01). However, there were no significant differences in FMD (-0.51 [-1.08-0.06]% vs. -0.58 [-1.20-0.04]%). Although the apolipoprotein B/apolipoprotein A1 ratio was significantly reduced in the Vilda group compared with baseline (0.66-0.62; p < 0.01), the change did not differ significantly between the two groups (-0.04 vs. 0.00; p = 0.27). Adiponectin levels were significantly increased in the Vilda group compared with the high Met group (0.75 mu g/mL vs. 0.01 mu g/mL; p < 0.01). Conclusions: Regardless of glycemic improvement, combination therapy of vildagliptin and metformin did not affect endothelial function but may exert favorable effects on adipokine levels and lipid profile in patients with type 2 diabetes without advanced atherosclerosis.
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页数:10
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