Statins in Low Doses Reduce VEGF and bFGF Serum Levels in Patients with Type 2 Diabetes Mellitus

被引:23
作者
Dworacka, Marzena [1 ]
Krzyzagorska, Ewa [3 ]
Wesolowska, Anna [1 ]
Borowska, Magdalena [1 ]
Iskakova, Saule [4 ]
Dworacki, Grzegorz [2 ]
机构
[1] Poznan Univ Med Sci, Dept Pharmacol, PL-60805 Poznan, Poland
[2] Poznan Univ Med Sci, Dept Clin Immunol, PL-60805 Poznan, Poland
[3] Poznan Specialist Ctr Med Care, Diabetol Outpatient Clin, Poznan, Poland
[4] West Kazakhstan State Med Univ, Dept Pharmacol, Aktobe, Kazakhstan
关键词
Angiogenesis; Statins; Type; 2; diabetes; Vascular endothelial growth factor; Basic fibroblast growth factor; ENDOTHELIAL GROWTH-FACTOR; PLACEBO-CONTROLLED TRIAL; HMG-COA REDUCTASE; CARDIOVASCULAR-DISEASE; ANGIOGENESIS; SIMVASTATIN; ATHEROSCLEROSIS; ATORVASTATIN; CORONARY; APOPTOSIS;
D O I
10.1159/000357476
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background/Aims: Recent experimental research revealed that statins at low doses induce angiogenesis, which in turn may be related to the course of atherosclerosis. There are no clinical studies evaluating the effect of 'low-dose' statins on serum levels of angiogenesis regulators in diabetic subjects. We aimed to explain how low doses of statins modify the serum concentrations of two potent proangiogenic factors, vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF), in patients with type 2 diabetes. Methods: Measurements of fasting glucose level, HbA(1c), 1,5-anhydro-D -glucitol and lipid profile were taken from 47 patients with type 2 diabetes treated with low doses of atorvastatin (10 mg daily) or simvastatin (10-20 mg daily), from 45 statin-free patients with type 2 diabetes and from 23 non-diabetic subjects. Measurements of VEGF and bFGF in serum were taken using the BD (TM) Cytometric Bead Array. Results and Conclusion: Statins used in low doses in patients with type 2 diabetes reduce the serum concentration of VEGF and bFGF which suggests antiangiogenic potential of these doses. Nevertheless, this effect could be neutralized by postprandial hyperglycemia. (C) 2014 S. Karger AG, Basel
引用
收藏
页码:32 / 38
页数:7
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