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腹主动脉瘤破裂的危险因素和小鼠模型。

Risk Factors and Mouse Models of Abdominal Aortic Aneurysm Rupture.

机构信息

The Vascular Biology Unit, Queensland Research Centre for Peripheral Vascular Disease, College of Medicine and Dentistry, James Cook University, Townsville, QLD 4811, Australia.

Australian Institute of Tropical Health and Medicine, James Cook University, Townsville, QLD 4811, Australia.

出版信息

Int J Mol Sci. 2020 Sep 30;21(19):7250. doi: 10.3390/ijms21197250.

Abstract

Abdominal aortic aneurysm (AAA) rupture is an important cause of death in older adults. In clinical practice, the most established predictor of AAA rupture is maximum AAA diameter. Aortic diameter is commonly used to assess AAA severity in mouse models studies. AAA rupture occurs when the stress (force per unit area) on the aneurysm wall exceeds wall strength. Previous research suggests that aortic wall structure and strength, biomechanical forces on the aorta and cellular and proteolytic composition of the AAA wall influence the risk of AAA rupture. Mouse models offer an opportunity to study the association of these factors with AAA rupture in a way not currently possible in patients. Such studies could provide data to support the use of novel surrogate markers of AAA rupture in patients. In this review, the currently available mouse models of AAA and their relevance to the study of AAA rupture are discussed. The review highlights the limitations of mouse models and suggests novel approaches that could be incorporated in future experimental AAA studies to generate clinically relevant results.

摘要

腹主动脉瘤(AAA)破裂是老年人死亡的一个重要原因。在临床实践中,AAA 破裂的最确定预测因子是 AAA 的最大直径。直径常用于评估小鼠模型研究中 AAA 的严重程度。当动脉瘤壁上的应力(单位面积上的力)超过壁强度时,就会发生 AAA 破裂。先前的研究表明,主动脉壁结构和强度、主动脉上的生物力学力以及 AAA 壁的细胞和蛋白水解组成影响 AAA 破裂的风险。小鼠模型提供了一个机会,可以在患者目前无法进行的情况下,研究这些因素与 AAA 破裂的关系。此类研究可以提供数据支持在患者中使用 AAA 破裂的新型替代标志物。在这篇综述中,讨论了目前可用于 AAA 的小鼠模型及其与 AAA 破裂研究的相关性。该综述强调了小鼠模型的局限性,并提出了未来实验性 AAA 研究中可以纳入的新方法,以产生与临床相关的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df67/7583758/84f89aaca748/ijms-21-07250-g001.jpg

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