Key result
Localised elastase treatment in ex vivo porcine aortic segments successfully caused elastin degradation and localized dilation under physiological pressures, emulating clinical aortic aneurysms.
Why the study?
Frequent device-related failures in endovascular aneurysm repairs highlight the need for test models that better represent the mural geometry and compliance changes in human aortic aneurysms.
Does localised elastase treatment in ex vivo porcine aortas emulate the morphological and mechanical changes of human aortic aneurysms?
Does localised elastase treatment in ex vivo porcine aortas emulate the morphological and mechanical changes of human aortic aneurysms?
Localised elastase treatment of ex vivo porcine aortas successfully creates a model that emulates the morphological and mechanical changes of human aortic aneurysms, providing a potential platform for testing endovascular devices.
May refine preclinical AA device testing; leaves open human tissue validation before clinical use.
Aortic aneurysms (AA) occur in 4.8% of people causing 150,000 deaths annually. While endovascular aneurysm repairs reduce surgical morbidity, device-related failures (leak/displacement) are frequent highlighting the need for test models that better represent the mural geometry and compliance changes in human AAs. We aimed to develop and characterise an ex vivo porcine aortic model of AA. The optimal duration of tissue elastase exposure to emulate AA changes in elastin microstructure and content was determined using porcine aortic rings. Elastase-induced changes were quantified morphologically, and mechanical properties assessed via ring tensile testing. Subsequent experiments tested the potential for localised elastase treatment in a 1 cm segment of porcine aorta using a specially designed 3D printed rig. The effect on pressure-diameter behaviour was investigated via inflation-extension testing. Elastase treatment produced time dependent decreases in elastin, resulting in an increased tensile modulus and circumferential length in the ring samples in the final phase of the J-shaped tissue stress-strain curves. In whole aortic segments, localised elastase-induced luminal degradation was successfully limited to a central region. The degree of elastin degradation achieved was sufficient to cause localised dilation with respect to controls under physiological pressures. Localised elastin degradation in porcine aortic segments is feasible and emulates the changes seen clinically in aortic aneurysms.
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Laffey et al. (2023) studied Aortic aneurysms. Localised elastase treatment vs. Controls was evaluated on Elastin degradation and localized dilation. Localised elastase treatment in ex vivo porcine aortic segments successfully caused elastin degradation and localized dilation under physiological pressures, emulating clinical aortic aneurysms.