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退行性主动脉瓣疾病的见解。

Insights into degenerative aortic valve disease.

作者信息

Goldbarg Seth H, Elmariah Sammy, Miller Marc A, Fuster Valentin

机构信息

Zena and Michael A. Wiener Cardiovascular Institute and Marie-Josée and Henry R. Kravis Cardiovascular Health Center, The Mount Sinai School of Medicine, New York, New York 10029, USA.

出版信息

J Am Coll Cardiol. 2007 Sep 25;50(13):1205-13. doi: 10.1016/j.jacc.2007.06.024. Epub 2007 Sep 10.

Abstract

Despite the dramatic decline of rheumatic heart disease over the past 5 decades, there has not been a concordant decline in the prevalence of valvular heart disease. Degenerative aortic valve disease (DAVD) has become the most common cause of valvular heart disease in the Western world, causing significant morbidity and mortality. No longer considered a benign consequence of aging, valve calcification is the result of an active process that, much like atherosclerotic vascular disease, is preceded by basement membrane disruption, inflammatory cell infiltration, and lipid deposition and is associated with diabetes, hypercholesterolemia, hypertension, and tobacco use. These realizations, in addition to pathological insights gained from emerging imaging modalities, have lead to the exploration of a variety of therapeutic interventions to delay or prevent the progression of DAVD. Inhibitors of 3-hydroxy-3-methylglutaryl-coenzyme A reductase, angiotensin-converting enzyme, and matrix metalloproteinase have all been studied as potential disease modifiers. Moreover, tissue engineering, aided by emerging stem cell technology, holds immense potential for the treatment of valvular heart disease as adjuncts to surgical interventions. Here we review the epidemiology and pathophysiology of DAVD, in addition to highlighting emerging therapeutic interventions for this growing problem.

摘要

尽管在过去50年里风湿性心脏病显著减少,但瓣膜性心脏病的患病率并未同步下降。退行性主动脉瓣疾病(DAVD)已成为西方世界瓣膜性心脏病最常见的病因,导致了显著的发病率和死亡率。瓣膜钙化不再被认为是衰老的良性后果,而是一个活跃过程的结果,这一过程很像动脉粥样硬化性血管疾病,在其之前会出现基底膜破坏、炎症细胞浸润和脂质沉积,并且与糖尿病、高胆固醇血症、高血压和吸烟有关。除了从新兴成像模式中获得的病理学见解外,这些认识还促使人们探索各种治疗干预措施,以延缓或预防DAVD的进展。3-羟基-3-甲基戊二酰辅酶A还原酶抑制剂、血管紧张素转换酶抑制剂和基质金属蛋白酶抑制剂都已作为潜在的疾病修饰剂进行了研究。此外,在新兴干细胞技术的辅助下,组织工程作为手术干预的辅助手段,在治疗瓣膜性心脏病方面具有巨大潜力。在此,我们除了强调针对这一日益严重问题的新兴治疗干预措施外,还将回顾DAVD的流行病学和病理生理学。

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