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二叶式主动脉瓣患者未扩张升主动脉壁的结构异常。

Structural abnormalities in the non-dilated ascending aortic wall of bicuspid aortic valve patients.

作者信息

Grewal Nimrat, Girdauskas Evaldas, Idhrees Mohammed, Velayudhan Bashi, Klautz Robert, Driessen Antoine, Poelmann Robert E

机构信息

Department of Cardiothoracic Surgery, Amsterdam University Medical Center, Amsterdam, the Netherlands; Department of Cardiothoracic Surgery, Leiden University Medical Center, Leiden, the Netherlands; Department of Anatomy and Embryology, Leiden University Medical Center, Leiden, the Netherlands.

Department of Cardiothoracic Surgery, University Hospital Augsburg, Augsburg, Germany.

出版信息

Cardiovasc Pathol. 2023 Jan-Feb;62:107478. doi: 10.1016/j.carpath.2022.107478. Epub 2022 Sep 23.

Abstract

BACKGROUND

A bicuspid aortic valve (BAV) is the most common congenital cardiac malformation. The development of the aortic valve is closely related to the development of the ascending aorta, associated with structural differences in the bicuspid aorta. Here we describe the non-dilated ascending aortic wall in bicuspid aortic valve patients.

METHODS

BAV (n=41) and tricuspid aortic valve (TAV) (n=18) non-dilated ascending aortic wall samples were studied. We investigated the following features of the aortic wall: vessel wall thickness, endothelial cell morphology, atherosclerosis, and elastic lamellae organization. Medial pathologic features encompassing elastic fiber thinning, fragmentation and degeneration, overall medial degeneration, mucoid extracellular matrix accumulation, and smooth muscle cell nuclei loss were studied. Furthermore, we included apoptosis, periaortic inflammation, and the level of expression of differentiated vascular smooth muscle cells.

RESULTS

The non-dilated BAV ascending aortic wall is characterized by a significantly thinner intimal layer, without features of atherosclerosis (P<.001). The medial layer is significantly thicker (P<.001) with more mucoid extracellular matrix accumulation (P<.001). All other medial pathologic features were more prominent in the TAV (P<.001). The media has significantly less differentiated vascular smooth muscle cells (P<.001) between the neatly regulated elastic lamellae which are thinner in the BAV as compared to the TAV (P<.0001).

CONCLUSIONS

The BAV ascending aorta without dilatation is characterized by a differentiation defect of vascular smooth muscle cells in the media and a significantly thinner intimal layer without overt pathologic features.

摘要

背景

二叶式主动脉瓣(BAV)是最常见的先天性心脏畸形。主动脉瓣的发育与升主动脉的发育密切相关,与二叶式主动脉的结构差异有关。在此,我们描述二叶式主动脉瓣患者未扩张的升主动脉壁。

方法

研究了41例二叶式主动脉瓣(BAV)和18例三叶式主动脉瓣(TAV)未扩张的升主动脉壁样本。我们研究了主动脉壁的以下特征:血管壁厚度、内皮细胞形态、动脉粥样硬化和弹性板组织。研究了中层病理特征,包括弹性纤维变薄、断裂和变性、整体中层变性、黏液样细胞外基质积聚和平滑肌细胞核丢失。此外,我们还纳入了细胞凋亡、主动脉周围炎症以及分化型血管平滑肌细胞的表达水平。

结果

未扩张的BAV升主动脉壁的特征是内膜层明显更薄,无动脉粥样硬化特征(P<0.001)。中层明显更厚(P<0.001),黏液样细胞外基质积聚更多(P<0.001)。所有其他中层病理特征在TAV中更明显(P<0.001)。与TAV相比,BAV中整齐排列的弹性板之间的中层分化型血管平滑肌细胞明显更少(P<0.001),且BAV中的弹性板更薄(P<0.0001)。

结论

未扩张的BAV升主动脉的特征是中层血管平滑肌细胞分化缺陷,内膜层明显更薄,无明显病理特征。

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