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遗传性胸主动脉疾病的基因筛查——基本原理、潜力与陷阱

Genetic screening in heritable thoracic aortic disease-rationale, potentials and pitfalls.

作者信息

Acharya Metesh, Maselli Daniele, Mariscalco Giovanni

机构信息

Department of Cardiac Surgery, Glenfield Hospital, Leicester, UK.

Department of Cardiac Surgery, European Hospital, Rome, Italy.

出版信息

Indian J Thorac Cardiovasc Surg. 2022 Apr;38(Suppl 1):24-35. doi: 10.1007/s12055-020-01124-7. Epub 2021 Mar 2.

Abstract

Thoracic aortic aneurysms are silent yet deadly clinical entities which may elude detection until an acutely life-threatening aortic dissection or rupture occurs. Approximately 20% of patients with thoracic aortic aneurysms or dissection have a positive family history, indicating a strong genetic component to the aetiology. Genetic screening in such hereditary thoracic aortic disease (HTAD) may thus be beneficial in detecting causative genetic mutations in affected patients, identifying asymptomatic family members who may be at risk, and in guiding the optimal timing of preventative surgery in those with confirmed genetic aortopathy. Genetic screening can facilitate personalised aortic care tailored to an individual's specific genetic abnormality, with the aim of mitigating the significant morbidity burden and premature mortality associated with HTAD. This review examines the rationale for genetic screening in HTAD, its potential applications, current limitations and potential future directions.

摘要

胸主动脉瘤是一种隐匿却致命的临床病症,在急性危及生命的主动脉夹层或破裂发生之前可能难以被发现。约20%的胸主动脉瘤或夹层患者有阳性家族史,这表明病因中存在很强的遗传因素。因此,对这种遗传性胸主动脉疾病(HTAD)进行基因筛查,可能有助于检测受影响患者的致病基因突变,识别可能有风险的无症状家庭成员,并指导确诊为遗传性主动脉病变患者进行预防性手术的最佳时机。基因筛查可促进针对个体特定基因异常的个性化主动脉护理,目的是减轻与HTAD相关的重大发病负担和过早死亡。本综述探讨了HTAD基因筛查的基本原理、其潜在应用、当前局限性及未来潜在方向。

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