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胶原蛋白更新对腹主动脉瘤自然病程影响的参数研究

Parametric study of effects of collagen turnover on the natural history of abdominal aortic aneurysms.

作者信息

Wilson J S, Baek S, Humphrey J D

机构信息

Department of Biomedical Engineering , Yale University , New Haven, CT 06520, USA.

出版信息

Proc Math Phys Eng Sci. 2013 Feb 8;469(2150):20120556. doi: 10.1098/rspa.2012.0556.

Abstract

Abdominal aortic aneurysms (AAAs) are characterized by significant changes in the architecture of the aortic wall, notably, loss of functional elastin and smooth muscle. Because collagen is the principal remaining load-bearing constituent of the aneurysmal wall, its turnover must play a fundamental role in the natural history of the lesion. Nevertheless, detailed investigations of the effects of different aspects of collagen turnover on AAA development are lacking. A finite-element membrane model of the growth and remodelling of idealized AAAs was thus used to investigate parametrically four of the primary aspects of collagen turnover: rates of production, half-life, deposition stretch (prestretch) and material stiffness. The predicted rates of aneurysmal expansion and spatio-temporal changes in wall thickness, biaxial stresses and maximum collagen fibre stretch at the apex of the lesion depended strongly on all four factors, as did the predicted clinical endpoints (i.e. arrest, progressive expansion or rupture). Collagen turnover also affected the axial expansion, largely due to mechanical changes within the shoulder region of the lesion. We submit, therefore, that assessment of rupture risk could be improved by future experiments that delineate and quantify different aspects of patient-specific collagen turnover and that such understanding could lead to new targeted therapeutics.

摘要

腹主动脉瘤(AAA)的特征是主动脉壁结构发生显著变化,尤其是功能性弹性蛋白和平滑肌的丧失。由于胶原蛋白是动脉瘤壁中剩余的主要承重成分,其更新必然在病变的自然病程中起重要作用。然而,目前缺乏对胶原蛋白更新的不同方面对AAA发展影响的详细研究。因此,使用理想化AAA生长和重塑的有限元膜模型,对胶原蛋白更新的四个主要方面进行参数研究:生成速率、半衰期、沉积拉伸(预拉伸)和材料刚度。预测的动脉瘤扩张速率以及病变顶端壁厚、双轴应力和最大胶原纤维拉伸的时空变化在很大程度上取决于所有这四个因素,预测的临床终点(即停滞、渐进性扩张或破裂)也是如此。胶原蛋白更新还影响轴向扩张,这主要是由于病变肩部区域的力学变化。因此,我们认为,未来通过描绘和量化患者特异性胶原蛋白更新的不同方面的实验可以改进破裂风险评估,并且这种认识可能会带来新的靶向治疗方法。

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