遗传学在胸主动脉瘤夹层风险分层中的作用

J. Rodrigues Bento, J. Meester, I. Luyckx, A. Verstraeten, B. Loeys
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引用次数: 0

摘要

胸主动脉瘤在西方人群中很普遍,通常是由基因缺陷引起的。如果未被发现,动脉瘤可以解剖或破裂,这是与高死亡率相关的事件。到目前为止,如果动脉瘤的大小达到一定的阈值,除了选择性手术外,没有其他治疗方法。在过去的几十年里,出现了基因型-表型关联,使临床医生能够开始根据解剖风险对患者进行分层。尽管如此,直到今天,风险评估仍因缺乏对潜在遗传学的充分理解和对遗传风险因素的修改而感到困惑,这些因素使尚未建立的基因型-表型相关性复杂化。专注于识别这些额外风险标志物的进一步研究至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Role of Genetics in Risk Stratification of Thoracic Aortic Aneurysm Dissection
Thoracic aortic aneurysms are prevalent in the Western population and are often caused by genetic defects. If undetected, aneurysms can dissect or rupture, which are events associated with a high mortality rate. Hitherto no cure exists other than elective surgery if aneurysm dimensions reach a certain threshold. In the past decades, genotype-phenotype associations have emerged that enable clinicians to start stratifying patients according to risk for dissection. Nonetheless, risk assessment is—to this day—confounded by the lack of full comprehension of underlying genetics and modifying genetic risk factors that complicate the yet established genotype-phenotype correlations. Further research that focuses on identifying these additional risk markers is crucial.
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