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Bicuspid aortic valve identifying knowledge gaps and rising to the challenge from the international bicuspid aortic valve consortium (BAVCON)

机译:二尖瓣主动脉瓣膜可识别知识差距并应对国际双尖瓣主动脉瓣膜联盟(BAVCON)的挑战

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摘要

Since its estimated first description >500 years ago by Leonardo da Vinci, the bicuspid aortic valve (BAV) has progressively built a reputation; initially, as a curious valvular phenotype with a tendency to develop obstruction and insufficiency. In more contemporary times, however, the BAV is recognized as underlying almost 50% of isolated severe aortic stenosis cases requiring surgery, and has been extensively associated with ominous outcomes such as bacterial endocarditis and aortic dissection. These associations, coupled with the high prevalence of BAV in humans, have prompted investigative efforts into the condition, which although insightful, have generated more questions than answers. This review describes our current knowledge of BAV, but, more importantly, it highlights knowledge gaps and areas where basic and clinical research is warranted. Our review has 2 sections. The first section outlines the multifaceted challenge of BAV, our current understanding of the condition, and barriers that may hamper the advancement of the science. The second section proposes a roadmap to discovery based on current imaging, molecular biology, and genetic tools, recognizing their advantages and limitations.
机译:自从莱昂纳多·达·芬奇(Leonardo da Vinci)于500年前对它的首次描述以来,双尖瓣主动脉瓣(BAV)逐渐赢得了声誉。最初,它是一种具有发展性阻塞和功能不足趋势的奇怪的瓣膜表型。然而,在更现代的时代,BAV被认为是需要手术的孤立严重主动脉瓣狭窄病例的近50%,并且已与不明结果(如细菌性心内膜炎和主动脉夹层)广泛相关。这些关联,再加上人类中BAV的高流行,促使人们对该病进行了调查研究,尽管这种研究颇有见识,但产生的问题多于答案。这篇评论描述了我们目前对BAV的了解,但更重要的是,它着重强调了需要进行基础和临床研究的知识空白和领域。我们的评论分为2节。第一部分概述了BAV的多方面挑战,我们目前对病情的理解以及可能阻碍科学发展的障碍。第二部分提出了基于当前成像,分子生物学和遗传工具的发现路线图,并认识到它们的优势和局限性。

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