The genetics and biomechanics of thoracic aortic diseases.

Vascular biology (Bristol, England) Pub Date : 2019-10-15 eCollection Date: 2019-01-01 DOI:10.1530/VB-19-0027
Amer Harky, Ka Siu Fan, Ka Hay Fan
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引用次数: 12

Abstract

Thoracic aortic aneurysms and aortic dissections (TAAD) are highly fatal emergencies within cardiothoracic surgery. With increasing age, thoracic aneurysms become more prevalent and pose an even greater threat when they develop into aortic dissections. Both diseases are multifactorial and are influenced by a multitude of physiological and biomechanical processes. Structural stability of aorta can be disrupted by genes, such as those for extracellular matrix and contractile protein, as well as telomere dysfunction, which leads to senescence of smooth muscle and endothelial cells. Biomechanical changes such as increased luminal pressure imposed by hypertension are also very prevalent and lead to structural instability. Furthermore, ageing is associated with a pro-inflammatory state that exacerbates degeneration of vessel wall, facilitating the development of both aortic aneurysms and aortic dissection. This literature review provides an overview of the aetiology and pathophysiology of both thoracic aneurysms and aortic dissections. With an improved understanding, new therapeutic targets may eventually be identified to facilitate treatment and prevention of these diseases.

Abstract Image

Abstract Image

胸主动脉疾病的遗传学和生物力学。
胸主动脉瘤和主动脉夹层(TAAD)是心胸外科中高度致命的急症。随着年龄的增长,胸动脉瘤变得越来越普遍,当它们发展成主动脉夹层时,会构成更大的威胁。这两种疾病都是多因素的,受到多种生理和生物力学过程的影响。细胞外基质、收缩蛋白等基因和端粒功能紊乱会破坏主动脉的结构稳定性,导致平滑肌和内皮细胞衰老。高血压引起的管腔压力升高等生物力学变化也非常普遍,并导致结构不稳定。此外,衰老与促炎状态有关,促炎状态加剧了血管壁的退化,促进了主动脉瘤和主动脉夹层的发展。本文综述了胸动脉瘤和主动脉夹层的病因学和病理生理学。随着认识的提高,新的治疗靶点可能最终被确定,以促进这些疾病的治疗和预防。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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