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二叶式主动脉瓣具有不同空间定向的瓣叶,是不同的病因实体。

Bicuspid aortic valves with different spatial orientations of the leaflets are distinct etiological entities.

机构信息

Department of Animal Biology, Faculty of Science, University of Málaga, Málaga, Spain.

出版信息

J Am Coll Cardiol. 2009 Dec 8;54(24):2312-8. doi: 10.1016/j.jacc.2009.07.044.

DOI:10.1016/j.jacc.2009.07.044
PMID:19958967
Abstract

OBJECTIVES

The aim of this study was to decide whether bicuspid aortic valves (BAVs) with fused right and noncoronary leaflets (R-N) and BAVs with fused right and left leaflets (R-L) have different etiologies or are the product of a single diathesis.

BACKGROUND

The BAV is the most common congenital cardiac malformation. The R-N and R-L BAVs are the most frequent BAV subtypes.

METHODS

The study was carried out in adult and embryonic hearts of endothelium nitric oxide synthase knock-out mice and inbred Syrian hamsters with a high incidence of R-N and R-L BAVs, respectively. The techniques used were histochemistry, immunohistochemistry, and scanning electron microscopy.

RESULTS

The R-N BAVs result from a defective development of the cardiac outflow tract (OT) endocardial cushions that generates a morphologically anomalous right leaflet. The left leaflet develops normally. The R-L BAVs are the outcome of an extrafusion of the septal and parietal OT ridges that thereby engenders a sole anterior leaflet. The noncoronary leaflet forms normally.

CONCLUSIONS

The R-N and R-L BAVs are different etiological entities. The R-N BAVs are the product of a morphogenetic defect that happens before the OT septation and that probably relies on an exacerbated nitric oxide-dependent epithelial-to-mesenchymal transformation. The R-L BAVs result from the anomalous septation of the proximal portion of the OT, likely caused by a distorted behavior of neural crest cells. Care should be taken in further work on BAV genetics because R-N and R-L BAVs might rely on different genotypes. Detailed screening for R-N and R-L BAVs should be performed for a better understanding of the relationships between these BAV morphologic phenotypes and other heart disease.

摘要

目的

本研究旨在确定融合右冠和无冠瓣的二叶主动脉瓣(BAV)与融合右和左瓣的二叶主动脉瓣(R-L)是否具有不同的病因,或者是否是单一病因的产物。

背景

BAV 是最常见的先天性心脏畸形。R-N 和 R-L BAV 是最常见的 BAV 亚型。

方法

该研究在内皮型一氧化氮合酶敲除小鼠的成年和胚胎心脏以及内源性叙利亚仓鼠中进行,这些仓鼠分别具有高发生率的 R-N 和 R-L BAV。使用的技术包括组织化学、免疫组织化学和扫描电子显微镜。

结果

R-N BAV 是由于心脏流出道(OT)心内膜垫发育缺陷引起的,该缺陷导致形态异常的右瓣。左瓣正常发育。R-L BAV 是由于间隔和壁 OT 嵴的额外融合引起的,从而产生单一的前瓣。无冠瓣正常形成。

结论

R-N 和 R-L BAV 是不同的病因实体。R-N BAV 是发生在 OT 分隔之前的形态发生缺陷的产物,可能依赖于强烈的一氧化氮依赖的上皮-间充质转化。R-L BAV 是近端 OT 异常分隔的结果,可能是由于神经嵴细胞的扭曲行为所致。在进一步的 BAV 遗传学研究中应谨慎行事,因为 R-N 和 R-L BAV 可能依赖于不同的基因型。应进行详细的 R-N 和 R-L BAV 筛查,以更好地了解这些 BAV 形态表型与其他心脏病之间的关系。

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