Division of Cardiology, The Heart Institute, Cincinnati Children's Hospital Medical Center, 240 Albert Sabin Way, Cincinnati, OH 45219, USA.
Cardiol Res Pract. 2012;2012:926975. doi: 10.1155/2012/926975. Epub 2012 Aug 27.
Bicuspid aortic valve (BAV) and thoracic aortic aneurysm (TAA) are two discrete cardiovascular phenotypes characterized by latent progressive disease states. There is a clear association between BAV and TAA; however the nature and extent of this relationship is unclear. There are both distinct and overlapping developmental pathways that have been established to contribute to the formation of the aortic valve and the aortic root, and the mature anatomy of these different tissue types is intimately intertwined. Likewise, human genetics studies have established apparently separate and common contributions to these clinical phenotypes, suggesting complex inheritance and a shared genetic basis and translating 3 patient populations, namely, BAV, TAA, or both, into a common but diverse etiology. A better understanding of the BAV-TAA association will provide an opportunity to leverage molecular information to modify clinical care through more sophisticated diagnostic testing, improved counseling, and ultimately new pharmacologic therapies.
二叶式主动脉瓣(BAV)和胸主动脉瘤(TAA)是两种以潜在进行性疾病状态为特征的离散心血管表型。BAV 和 TAA 之间存在明显的关联;然而,这种关系的性质和程度尚不清楚。已经确定了明确的和重叠的发育途径,这些途径有助于形成主动脉瓣和主动脉根部,并且这些不同组织类型的成熟解剖结构紧密交织。同样,人类遗传学研究已经确定了对这些临床表型的明显独立和共同贡献,表明复杂的遗传和共同的遗传基础,并将 3 种患者群体,即 BAV、TAA 或两者,转化为共同但多样化的病因。更好地了解 BAV-TAA 关联将提供一个机会,通过更复杂的诊断测试、改进的咨询以及最终新的药物治疗来利用分子信息来改变临床护理。