Atorvastatin has antithrombotic effects in patients with type 1 diabetes and dyslipidemia

被引:57
|
作者
Tehrani, Sara [1 ]
Mobarrez, Fariborz [2 ]
Antovic, Aleksandra [1 ]
Santesson, Pia [1 ]
Lins, Per-Eric [1 ]
Adamson, Ulf [1 ]
Henriksson, Peter [2 ]
Wallen, N. Hakan [2 ]
Jorneskog, Gun [1 ]
机构
[1] Karolinska Inst, Danderyd Hosp, Div Internal Med, Dept Clin Sci, S-18288 Danderyd, Sweden
[2] Karolinska Inst, Danderyd Hosp, Div Cardiovasc Med, Dept Clin Sci, S-18288 Danderyd, Sweden
关键词
Atorvastatin; Fibrin network; Microparticles; Diabetes; PLATELET-DERIVED MICROPARTICLES; FIBRIN GEL STRUCTURE; TISSUE FACTOR; P-SELECTIN; ROSUVASTATIN; CHOLESTEROL; SIMVASTATIN; PREVENTION; THERAPY;
D O I
10.1016/j.thromres.2010.05.023
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Diabetes is a prothrombotic state involving a more thrombogenic fibrin network. In the present study we investigated the effects of lipid-lowering therapy with atorvastatin on fibrin network structure and platelet-derived microparticles in patients with type 1 diabetes and dyslipidemia. Materials and Methods: Twenty patients were treated with atorvastatin (80 mg daily) or placebo during 2 months in a randomized, double-blind, cross-over study. Fibrin network permeability, expression of glycoprotein IIIa, P-selectin and tissue factor on platelet-derived microparticles, plasma endogenous thrombin potential, plasminogen activator inhibitor-1 and tissue plasminogen activator antigen levels were assessed. Additionally, levels of plasma fibrinogen, high-sensitivity C-reactive protein and glycated haemoglobin were measured. Results: During treatment with atorvastatin, fibrin network permeability increased (p = 0.01), while endogenous thrombin potential and expression of glycoprotein IIIa, P-selectin and tissue factor decreased (p < 0.01). In vitro experiments indicated that platelet-derived microparticles influence the fibrin network formation as fibrin network permeability decreased significantly when platelet-derived microparticles were added to normal plasma. Baseline levels of plasminogen activator inhibitor-1 and tissue plasminogen activator antigen as well as plasma fibrinogen and high-sensitivity C-reactive protein were within reference values and not significantly changed during atorvastatin treatment, while glycated haemoglobin increased 0.3% (p < 0.001). Conclusions: Novel treatment effects were found in patients with type 1 diabetes and dyslipidemia during atorvastatin therapy, i.e. a more porous fibrin network, to which reduced expression of glycoprotein IIIa, P-selectin and tissue factor on platelet-derived microparticles may contribute. The observed impairment of glycemic control during long-term statin treatment deserves attention. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:E225 / E231
页数:7
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