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
相关论文
共 50 条
  • [21] Combined lipid goal attainment in patients with type 2 diabetes and dyslipidemia: A head-to-head comparative trial of statins
    Wu, Tsung-Hui
    Lee, I-Te
    Ho, Low-Tone
    Sheu, Wayne H-H
    Hwu, Chii-Min
    JOURNAL OF THE CHINESE MEDICAL ASSOCIATION, 2022, 85 (08) : 831 - 838
  • [22] Acute Effects of Atorvastatin on Glomerular Filtration Rate, Tubular Function, Blood Pressure, and Vasoactive Hormones in Patients With Type 2 Diabetes
    Paulsen, L.
    Matthesen, S. K.
    Bech, J. N.
    Starklint, J.
    Pedersen, E. B.
    JOURNAL OF CLINICAL PHARMACOLOGY, 2010, 50 (07): : 816 - 822
  • [23] Long-term effects following 4 years of randomized treatment with atorvastatin in patients with type 2 diabetes mellitus on hemodialysis
    Krane, Vera
    Schmidt, Kay-Renke
    Gutjahr-Lengsfeld, Lena J.
    Mann, Johannes F. E.
    Maerz, Winfried
    Swoboda, Florian
    Wanner, Christoph
    KIDNEY INTERNATIONAL, 2016, 89 (06) : 1380 - 1387
  • [24] Efficacy and safety of fenofibric acid in combination with atorvastatin and ezetimibe in patients with mixed dyslipidemia
    Jones, Peter H.
    Goldberg, Anne C.
    Knapp, Howard R.
    Kelly, Maureen T.
    Setze, Carolyn M.
    Stolzenbach, James C.
    Sleep, Darryl J.
    AMERICAN HEART JOURNAL, 2010, 160 (04) : 759 - 766
  • [25] Effects of atorvastatin on apelin, visfatin (nampt), ghrelin and early carotid atherosclerosis in patients with type 2 diabetes
    Kadoglou, Nikolaos P. E.
    Sailer, Nikolaos
    Kapelouzou, Alkistis
    Lampropoulos, Stylianos
    Vitta, Ioulia
    Kostakis, Alkiviadis
    Liapis, Christos D.
    ACTA DIABETOLOGICA, 2012, 49 (04) : 269 - 276
  • [26] Short Term Effects of Atorvastatin on Endothelial Functions and Oxidized LDL Levels in Patients with Type 2 Diabetes
    Akalin, Aysen
    Temiz, Gokhan
    Akcar, Nevbahar
    Sensoy, Banu
    ENDOCRINE JOURNAL, 2008, 55 (05) : 861 - 866
  • [27] Baseline characteristics in the Collaborative AtoRvastatin Diabetes Study (CARDS) in patients with Type 2 diabetes
    Thomason, MJ
    Colhoun, HM
    Livingstone, SJ
    Mackness, MI
    Betteridge, DJ
    Durrington, PN
    Hitman, GA
    Neil, HAW
    Fuller, JH
    DIABETIC MEDICINE, 2004, 21 (08) : 901 - 905
  • [28] Effect of ezetimibe/simvastatin compared with atorvastatin on lipoprotein subclasses in patients with type 2 diabetes and hypercholesterolaemia
    Tomassini, J. E.
    Mazzone, T.
    Goldberg, R. B.
    Guyton, J. R.
    Weinstock, R. S.
    Polis, A.
    Jensen, E.
    Tershakovec, A. M.
    DIABETES OBESITY & METABOLISM, 2009, 11 (09): : 855 - 864
  • [29] Efficacy of Moderate Intensity Statins in the Treatment of Dyslipidemia in Korean Patients with Type 2 Diabetes Mellitus
    Kong, Sung Hye
    Koo, Bo Kyung
    Moon, Min Kyong
    DIABETES & METABOLISM JOURNAL, 2017, 41 (01) : 23 - 30
  • [30] The effects of pitavastatin on glucose metabolism in patients with type 2 diabetes with hypercholesterolemia
    Daido, Hisashi
    Horikawa, Yukio
    Takeda, Jun
    DIABETES RESEARCH AND CLINICAL PRACTICE, 2014, 106 (03) : 531 - 537