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Dilatation of the Aorta in Bicuspid Aortic Valve Disease.

作者信息

Simpson John M, Pushparajah Kuberan

机构信息

Department of Congenital Heart Disease, Evelina London Children's Hospital, Guy's and St Thomas' NHS Trust, United Kingdom. Division of Biomedical Engineering and Imaging Sciences, King's College London, St Thomas Hospital, United Kingdom.

出版信息

Circ Cardiovasc Imaging. 2020 Mar;13(3):e010448. doi: 10.1161/CIRCIMAGING.120.010448. Epub 2020 Mar 17.

DOI:10.1161/CIRCIMAGING.120.010448
PMID:32178535
Abstract
摘要

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Dilatation of the Aorta in Bicuspid Aortic Valve Disease.二叶式主动脉瓣疾病中的主动脉扩张
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Monocyte-to-HDL-cholesterol ratio is associated with Ascending Aorta Dilatation in Patients with Bicuspid Aortic Valve.单核细胞/高密度脂蛋白胆固醇比值与二叶式主动脉瓣患者升主动脉扩张相关。
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Long-Term Risk Factors for Dilatation of the Proximal Aorta in a Large Cohort of Children With Bicuspid Aortic Valve.二叶式主动脉瓣患儿大队列中升主动脉扩张的长期风险因素。
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Long-term Fate of Dilated Ascending Aorta after Aortic Valve Replacement for Bicuspid Versus Tricuspid Aortic Valve Disease.主动脉瓣置换术后二叶式主动脉瓣与三叶式主动脉瓣病变患者升主动脉扩张的长期转归。
Am J Cardiol. 2020 Aug 15;129:53-59. doi: 10.1016/j.amjcard.2020.05.026. Epub 2020 May 26.
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Circulating matrix metalloproteinase patterns in association with aortic dilatation in bicuspid aortic valve patients with isolated severe aortic stenosis.孤立性严重主动脉瓣狭窄的二叶式主动脉瓣患者中循环基质金属蛋白酶模式与主动脉扩张的关系
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Case 3/2015 A 32-year-old female patient with coarctation of the aorta, bicuspid aortic valve and dilatation of the ascending aorta.病例3/2015：一名32岁女性患者，患有主动脉缩窄、二叶式主动脉瓣和升主动脉扩张。
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J Thorac Cardiovasc Surg. 2013 Sep;146(3):605-10. doi: 10.1016/j.jtcvs.2012.07.039. Epub 2012 Sep 13.

引用本文的文献

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Aortic valve replacement in a bicuspid aortic valve patient followed by reoperation for ascending aorta rupture: a case report.一例二叶式主动脉瓣患者行主动脉瓣置换术后因升主动脉破裂再次手术的病例报告。
Front Cardiovasc Med. 2024 Dec 11;11:1471686. doi: 10.3389/fcvm.2024.1471686. eCollection 2024.
2
The Predictive Role of Plasma Biomarkers in the Evolution of Aortopathies Associated with Congenital Heart Malformations.血浆生物标志物在先天性心脏畸形相关主动脉病变演变中的预测作用。
Int J Mol Sci. 2022 Apr 30;23(9):4993. doi: 10.3390/ijms23094993.
3
Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease.
导致原钙黏蛋白α缺乏的常见缺失变异体促成了二叶式主动脉瓣和左侧先天性心脏病的复杂遗传学。
HGG Adv. 2021 Jul 8;2(3). doi: 10.1016/j.xhgg.2021.100037. Epub 2021 Jul 29.