钙化
心脏瓣膜
主动脉瓣
医学
疾病
体内
瓣膜性心脏病
阀门更换
病理
心脏病学
生物
生物技术
狭窄
作者
Zijin Zhu,Zhirong Liu,Donghui Zhang,Li Li,Jianqiu Pei,Lin Cai
标识
DOI:10.1186/s13619-024-00189-8
摘要
Abstract Calcific Aortic Valve Disease (CAVD) is prevalent among the elderly as the most common valvular heart disease. Currently, no pharmaceutical interventions can effectively reverse or prevent CAVD, making valve replacement the primary therapeutic recourse. Extensive research spanning decades has contributed to the establishment of animal and in vitro cell models, which facilitates a deeper understanding of the pathophysiological progression and underlying mechanisms of CAVD. In this review, we provide a comprehensive summary and analysis of the strengths and limitations associated with commonly employed models for the study of valve calcification. We specifically emphasize the advancements in three-dimensional culture technologies, which replicate the structural complexity of the valve. Furthermore, we delve into prospective recommendations for advancing in vivo and in vitro model studies of CAVD.
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