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二叶式主动脉瓣疾病及主动脉狭窄/关闭不全作为胸主动脉瘤危险因素的意义

Implications of Bicuspid Aortic Valve Disease and Aortic Stenosis/Insufficiency as Risk Factors for Thoracic Aortic Aneurysm.

作者信息

Jabagi Habib, Levine Dov, Gharibeh Lara, Camillo Chiara, Castillero Estibaliz, Ferrari Giovanni, Takayama Hiroo, Grau Juan B

机构信息

Division of Cardiothoracic Surgery, The Valley Hospital, NJ 07450, USA.

Department of Cardiovascular Surgery, Mt. Sinai Hospital, Icahn School of Medicine, New York, NY 10029, USA.

出版信息

Rev Cardiovasc Med. 2023 Jun 19;24(6):178. doi: 10.31083/j.rcm2406178. eCollection 2023 Jun.

Abstract

Bicuspid Aortic Valves (BAV) are associated with an increased incidence of thoracic aortic aneurysms (TAA). TAA are a common aortic pathology characterized by enlargement of the aortic root and/or ascending aorta, and may become life threatening when left untreated. Typically occurring as the sole pathology in a patient, TAA are largely asymptomatic. However, in some instances, they are accompanied by aortic valve (AV) diseases: either congenital BAV or acquired in the form of Aortic Insufficiency (AI) or aortic stenosis (AS). When TAA are associated with aortic valve disease, determining an accurate and predictable prognosis becomes especially challenging. Patients with AV disease and concomitant TAA lack a widely accepted diagnostic approach, one that integrates our knowledge on aortic valve pathophysiology and encompasses multi-modality imaging approaches. This review summarizes the most recent scientific knowledge regarding the association between AV diseases (BAV, AI, AS) and ascending aortopathies (dilatation, aneurysm, and dissection). We aimed to pinpoint the gaps in monitoring practices and prediction of disease progression in TAA patients with concomitant AV disease. We propose that a morphological and functional analysis of the AV with multi-modality imaging should be included in aortic surveillance programs. This strategy would allow for improved risk stratification of these patients, and possibly new AV phenotypic-specific guidelines with more vigilant surveillance and earlier prophylactic surgery to improve patient outcomes.

摘要

二叶式主动脉瓣(BAV)与胸主动脉瘤(TAA)的发病率增加相关。TAA是一种常见的主动脉病变,其特征是主动脉根部和/或升主动脉扩大,若不治疗可能会危及生命。TAA通常是患者唯一的病变,大多无症状。然而,在某些情况下,它们会伴有主动脉瓣(AV)疾病:先天性BAV或以主动脉瓣关闭不全(AI)或主动脉狭窄(AS)形式出现的后天性疾病。当TAA与主动脉瓣疾病相关时,确定准确且可预测的预后变得尤其具有挑战性。患有AV疾病并伴有TAA的患者缺乏一种广泛接受的诊断方法,即一种整合我们对主动脉瓣病理生理学的认识并涵盖多模态成像方法的诊断方法。本综述总结了关于AV疾病(BAV、AI、AS)与升主动脉病变(扩张、动脉瘤和夹层)之间关联的最新科学知识。我们旨在找出在伴有AV疾病的TAA患者的监测实践和疾病进展预测方面的差距。我们建议在主动脉监测项目中纳入对AV进行多模态成像的形态学和功能分析。这一策略将改善这些患者的风险分层,并可能制定新的针对AV表型特异性的指南,进行更密切的监测和更早的预防性手术以改善患者预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0d1/11264121/76301ee6a60d/2153-8174-24-6-178-g1.jpg

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