Aortic Valve Stenosis From Basic Mechanisms to Novel Therapeutic Targets

被引:228
作者
Goody, Philip Roger [1 ]
Hosen, Mohammed Rabiul [1 ]
Christmann, Dominik [1 ]
Niepmann, Sven Thomas [1 ]
Zietzer, Andreas
Adam, Matti [2 ]
Boenner, Florian [3 ]
Zimmer, Sebastian [1 ]
Nickenig, Georg [1 ]
Jansen, Felix [1 ]
机构
[1] Univ Hosp Bonn, Dept Med 2, Heart Ctr Bonn, Venusberg Campus 1, D-53127 Bonn, Germany
[2] Univ Hosp Cologne, Clin Internal Med 2, Cologne, Germany
[3] Univ Hosp Dusseldorf, Clin Cardiol Pulmonol & Angiol, Dusseldorf, Germany
关键词
aortic valve; aortic valve stenosis; calcification; heart valve disease; inflammation; valvular endothelial cells; valvular interstitial cells; VALVULAR INTERSTITIAL-CELLS; PROMOTE OSTEOBLAST DIFFERENTIATION; ENDOTHELIAL GROWTH-FACTOR; LOW-DENSITY-LIPOPROTEIN; VASCULAR CALCIFICATION; OSTEOCLAST DIFFERENTIATION; OSTEOGENIC PHENOTYPE; OXIDATIVE STRESS; CLINICAL FACTORS; MATRIX VESICLES;
D O I
10.1161/ATVBAHA.119.313067
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aortic valve stenosis is the most prevalent heart valve disease worldwide. Although interventional treatment options have rapidly improved in recent years, symptomatic aortic valve stenosis is still associated with high morbidity and mortality. Calcific aortic valve stenosis is characterized by a progressive fibro-calcific remodeling and thickening of the aortic valve cusps, which subsequently leads to valve obstruction. The underlying pathophysiology is complex and involves endothelial dysfunction, immune cell infiltration, myofibroblastic and osteoblastic differentiation, and, subsequently, calcification. To date, no pharmacotherapy has been established to prevent aortic valve calcification. However, novel promising therapeutic targets have been recently identified. This review summarizes the current knowledge of pathomechanisms involved in aortic valve calcification and points out novel treatment strategies.
引用
收藏
页码:885 / 900
页数:16
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