胸主动脉瘤和腹主动脉瘤相关基因的比较

Q3 Medicine AORTA Pub Date : 2023-06-01 Epub Date: 2023-06-06 DOI:10.1055/s-0043-57266
Argyrios Gyftopoulos, Bulat A Ziganshin, John A Elefteriades, Cassius I Ochoa Chaar
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引用次数: 0

摘要

影响升胸主动脉和腹主动脉的动脉瘤会影响具有不同临床特征的患者群体。通过文献综述,本文比较了升胸主动脉瘤(ATAA)与腹主动脉瘤(AAA)的遗传关联。与动脉粥样硬化、脂质代谢和肿瘤发生有关的基因与散发性 AAA 特别相关,而控制细胞外基质(ECM)结构、ECM 重塑和肿瘤生长因子 β 功能的基因与 AAA 和 ATAA 都相关。收缩元件基因是导致 ATAA 的独特诱因。除了已知的综合结缔组织病和多动脉瘤综合征(马凡病、Loeys-Dietz 综合征和 Ehlers-Danlos 综合征)外,AAA 和 ATAA 之间的遗传重叠非常有限。基因分型和生物信息学的飞速发展将进一步阐明与影响主动脉各部位动脉瘤发病相关的各种途径。
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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Comparison of Genes Associated with Thoracic and Abdominal Aortic Aneurysms.

Aneurysms impacting the ascending thoracic aorta and the abdominal aorta affect patient populations with distinct clinical characteristics. Through a literature review, this paper compares the genetic associations of ascending thoracic aortic aneurysm (ATAA) with abdominal aortic aneurysms (AAA). Genes related to atherosclerosis, lipid metabolism, and tumor development are associated specifically with sporadic AAA, while genes controlling extracellular matrix (ECM) structure, ECM remodeling, and tumor growth factor β function are associated with both AAA and ATAA. Contractile element genes uniquely predispose to ATAA. Aside from known syndromic connective tissue disease and poly-aneurysmal syndromes (Marfan disease, Loeys-Dietz syndrome, and Ehlers-Danlos syndrome), there is only limited genetic overlap between AAA and ATAA. The rapid advances in genotyping and bioinformatics will elucidate further the various pathways associated with the development of aneurysms affecting various parts of the aorta.

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来源期刊
AORTA
AORTA Medicine-Surgery
CiteScore
1.00
自引率
0.00%
发文量
119
期刊最新文献
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