Aortic stenosis and the haemostatic system

被引:9
作者
Trimaille, Antonin [1 ,2 ]
Hmadeh, Sandy [2 ]
Matsushita, Kensuke [1 ,2 ]
Marchandot, Benjamin [1 ]
Kauffenstein, Gilles [2 ]
Morel, Olivier [1 ,2 ]
机构
[1] Strasbourg Univ Hosp, Nouvel Hop Civil, Dept Cardiovasc Med, 1 Pl lhop, F-67000 Strasbourg, France
[2] INSERM, UMR 1260, French Natl Inst Hlth & Med Res, Regenerat Nanomed,FMTS, 1 Rue Eugene Boeckel, F-67000 Strasbourg, France
关键词
Aortic stenosis; Haemostasis; Thrombosis; Transcatheter aortic valve replacement; VALVE INTERSTITIAL-CELLS; VON-WILLEBRAND-FACTOR; SUBCLINICAL LEAFLET THROMBOSIS; SHED MEMBRANE MICROPARTICLES; PLATELET-DERIVED TGF-BETA-1; MOLECULAR-WEIGHT MULTIMERS; ESC WORKING GROUP; TISSUE FACTOR; ENDOTHELIAL-CELLS; TRANSFORMING GROWTH-FACTOR-BETA-1;
D O I
10.1093/cvr/cvac192
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aortic stenosis (AS) affects more than 10% of the population over 80 years of age and constitutes a major risk factor for heart failure, thromboembolic stroke, and death. A better understanding of the disease, including its interaction with the haemostatic system, is a prerequisite to develop prophylactic treatments. AS pathogenesis is a dynamic process involving endothelial dysfunction, inflammation, fibrosis, and calcification. Several studies support the interplay between the components of the haemostatic system such as platelets, the coagulation system, von Willebrand factor, and extracellular micro-particles at each pathophysiological stage of AS. Previous reports have evidenced persistent biological activity of the native valve after transcatheter aortic valve replacement and the subsequent development of microthrombosis that may impact the function of the newly implanted valve. Here, we review the current evidence on the interplay between AS and prothrombotic activity, and we emphasize the clinical consequences of these interactions after aortic valve replacement.
引用
收藏
页码:1310 / 1323
页数:14
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