Temporal evolution of mechanical stimuli from vascular remodeling in response to the severity and duration of aortic coarctation

Author:

Azarnoosh Jamasp1,Ghorbannia Arash1,Ibrahim El-Sayed H.2,Jurkiewicz Hilda1,Kalvin Lindsey2,LaDisa John F.1

Affiliation:

1. Marquette University and the Medical College of Wisconsin

2. Medical College of Wisconsin

Abstract

Abstract Coarctation of the aorta (CoA) is one of the most common congenital cardiovascular diseases. CoA patients frequently undergo surgical repair, but hypertension (HTN) is still common. The current treatment guideline has revealed irreversible changes in structure and function, yet revised severity guidelines have not been proposed. Our objective was to quantify temporal alterations in mechanical stimuli and changes in arterial geometry in response to the range of CoA severities and durations seen clinically. Rabbits were exposed to CoA resulting in BPGpp severities of ≤ 10, 10–20, and ≥ 20 mmHg for a duration of ~ 1, 3, or 20 weeks using permanent, dissolvable, and rapidly dissolvable sutures. Elastic moduli and thickness were estimated from imaging and longitudinal fluid-structure interaction (FSI) simulations were conducted at different ages using geometries and boundary conditions measured empirically. Mechanical stimuli were characterized including blood flow velocity patterns, wall tension, and radial strain. Empirical results show vascular alternations including thickening and stiffening proximal to the coarctation with increasing severity and/or duration of CoA. FSI simulations indicate wall tension in the proximal region increases markedly with coarctation severity. Importantly, even mild CoA induced stimuli for remodeling that exceeds values seen in adulthood if not treated early and using a BPGpp lower than the current clinical threshold. The findings are aligned with observations from other species and provide some guidance for the values of mechanical stimuli that could be used to predict the likelihood of HTN in human patients with CoA.

Publisher

Research Square Platform LLC

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