胸主动脉动脉瘤的遗传

IF 0.4 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY
Margaux Cadenet, Nadine Hanna, Pauline Arnaud
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引用次数: 0

摘要

胸主动脉瘤对应于主动脉上升部分的扩张,这可能导致夹层(TAAD为胸主动脉瘤和夹层)或主动脉破裂。病因多种多样,但在大约20%的病例中发现遗传来源。据报道,大约有30个基因与TAAD的发展有关。这些基因中的大多数编码参与细胞外基质、平滑肌细胞收缩或生长因子TGF-β信号通路的蛋白质。确定导致主动脉疾病的致病变异对于做出明确诊断、指导和个性化患者治疗以及筛查有风险的亲属至关重要。随着新测序技术(下一代测序)的发展和基因面板的使用,基因检测的可获得性和可及性已大大提高。本文综述了与TAAD相关的主要基因以及目前的诊断策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic of thoracic aorta aneurysm

The thoracic aortic aneurysm corresponds to the dilation of the ascending part of the aorta, which can lead to a dissection (TAAD for Thoracic Aortic Aneurysm and Dissection) or aortic rupture. The etiologies are diverse, but in approximately 20% of cases a genetic origin is found. About thirty genes are reported to be responsible for the development of TAAD. The majority of these genes encode for proteins involved in the extracellular matrix, the contraction of smooth muscle cells or the growth factor TGF-β signaling pathway. Identifying the pathogenic variant responsible for the aortic disease becomes essential to make a definitive diagnosis, to guide and to personalize the treatment of the patients but also to screen relatives at risk. The availability and access to genetic testing have improved considerably with the development of new sequencing techniques (NGS for Next Generation Sequencing) and the use of gene panels. This review summarizes the main genes associated with TAAD as well as the current diagnostic strategy.

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来源期刊
Annales de biologie clinique
Annales de biologie clinique 医学-医学:研究与实验
CiteScore
0.80
自引率
20.00%
发文量
53
审稿时长
6-12 weeks
期刊介绍: Multidisciplinary information with direct relevance to everyday practice Annales de Biologie Clinique, the official journal of the French Society of Clinical Biology (SFBC), supports biologists in areas including continuing education, laboratory accreditation and technique validation. With original articles, abstracts and accounts of everyday practice, the journal provides details of advances in knowledge, techniques and equipment, as well as a forum for discussion open to the entire community.
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