Off-target effects of oral anticoagulants - vascular effects of vitamin K antagonist and non-vitamin K antagonist oral anticoagulant dabigatran etexilate

被引:19
作者
van Gorp, Rick H. [1 ,2 ]
Dijkgraaf, Ingrid [1 ]
Broker, Vanessa [1 ]
Bauwens, Matthias [3 ]
Leenders, Peter [1 ]
Jennen, Danyel [4 ]
Dweck, Marc R. [5 ]
Bucerius, Jan [3 ]
Briede, Jacco J. [4 ]
van Ryn, Joanne [6 ]
Brandenburg, Vincent [7 ]
Mottaghy, Felix [3 ,8 ]
Spronk, Henri M. H. [1 ]
Reutelingsperger, Chris P. [1 ]
Schurgers, Leon J. [1 ,9 ]
机构
[1] Maastricht Univ, Cardiovasc Res Inst Maastricht, Dept Biochem, Maastricht, Netherlands
[2] Nattopharma ASA, Oslo, Norway
[3] Maastricht Univ Med Ctr MUMC, Dept Radiol & Nucl Med, Maastricht, Netherlands
[4] Maastricht Univ, GROW Sch Oncol & Dev Biol, Dept Toxicogen, Maastricht, Netherlands
[5] Univ Edinburgh, Ctr Cardiovasc Sci, Edinburgh, Midlothian, Scotland
[6] Boehringer Ingelheim GmbH & Co KG, Dept Cardiometab Res, Biberach, Germany
[7] Rhein Maas Klinikum Wurselen, Klin Kardiol & Nephrol, Wurselen, Germany
[8] Rhein Westfal TH Aachen, Univ Hosp, Dept Nucl Med, Aachen, Germany
[9] Rhein Westfal TH Aachen, Inst Expt Med & Syst Biol, Aachen, Germany
基金
欧盟地平线“2020”;
关键词
atherosclerosis; NOAC; oxidative stress; vascular calcification; vascular smooth muscle cells; VKA; MATRIX GLA-PROTEIN; CORONARY-ARTERY CALCIUM; THROMBIN INHIBITION; MYOCARDIAL-INFARCTION; CALCIFICATION; WARFARIN; PLAQUE; ATHEROSCLEROSIS; PROGRESSION; DENSITY;
D O I
10.1111/jth.15289
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Vitamin K antagonists (VKA) and non-vitamin K oral antagonist anticoagulants (NOAC) are used in the clinic to reduce risk of thrombosis. However, they also exhibit vascular off-target effects. The aim of this study is to compare VKA and NOAC on atherosclerosis progression and calcification in an experimental setup. Material and methods Female Apoe(-/-) mice (age 12 weeks) were fed Western-type diet as control or supplemented with dabigatran etexilate or warfarin for 6 or 18 weeks. Vascular calcification was measured in whole aortic arches using mu CT and [F-18]-NaF. Atherosclerotic burden was assessed by (immuno)histochemistry. Additionally, in vitro effects of warfarin, thrombin, and dabigatran on primary vascular smooth muscle cells (VSMC) were assessed. Results Short-term treatment with warfarin promoted formation of atherosclerotic lesions with a pro-inflammatory phenotype, and more rapid plaque progression compared with control and dabigatran. In contrast, dabigatran significantly reduced plaque progression compared with control. Long-term warfarin treatment significantly increased both presence and activity of plaque calcification compared with control and dabigatran. Calcification induced by warfarin treatment was accompanied by increased presence of uncarboxylated matrix Gla protein. In vitro, both warfarin and thrombin significantly increased VSMC oxidative stress and extracellular vesicle release, which was prevented by dabigatran. Conclusion Warfarin aggravates atherosclerotic disease activity, increasing plaque inflammation, active calcification, and plaque progression. Dabigatran lacks undesired vascular side effects and reveals beneficial effects on atherosclerosis progression and calcification. The choice of anticoagulation impacts atherosclerotic disease by differential off target effect. Future clinical studies should test whether this beneficial effect also applies to patients.
引用
收藏
页码:1348 / 1363
页数:16
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