Aortic Remodeling Kinetics in Response to Coarctation-Induced Mechanical Perturbations

Author:

Ghorbannia Arash123ORCID,Maadooliat Mehdi4ORCID,Woods Ronald K.5,Audi Said H.1,Tefft Brandon J.1,Chiastra Claudio6ORCID,Ibrahim El Sayed H.17ORCID,LaDisa John F.1238ORCID

Affiliation:

1. Joint Department of Biomedical Engineering, Medical College of Wisconsin, Marquette University, Milwaukee, WI 53226, USA

2. Section of Pediatric Cardiology, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI 53226, USA

3. Herma Heart Institute, Children’s Wisconsin, Milwaukee, WI 53226, USA

4. Department of Mathematical and Statistical Sciences, Marquette University, Milwaukee, WI 53233, USA

5. Division of Pediatric Cardiothoracic Surgery, Department of Surgery, Medical College of Wisconsin, Herma Heart Institute, Children’s Wisconsin, Milwaukee, WI 53226, USA

6. PoliToBIOMed Lab, Department of Mechanical and Aerospace Engineering, Politecnico di Torino, 10129 Turin, Italy

7. Department of Radiology, Medical College of Wisconsin, Milwaukee, WI 53226, USA

8. Department of Physiology, Medical College of Wisconsin, Milwaukee, WI 53226, USA

Abstract

Background: Coarctation of the aorta (CoA; constriction of the proximal descending thoracic aorta) is among the most common congenital cardiovascular defects. Coarctation-induced mechanical perturbations trigger a cycle of mechano-transduction events leading to irreversible precursors of hypertension including arterial thickening, stiffening, and vasoactive dysfunction in proximal conduit arteries. This study sought to identify kinetics of the stress-mediated compensatory response leading to these alterations using a preclinical rabbit model of CoA. Methods: A prior growth and remodeling (G&R) framework was reformulated and fit to empirical measurements from CoA rabbits classified into one control and nine CoA groups of various severities and durations (n = 63, 5–11/group). Empirical measurements included Doppler ultrasound imaging, uniaxial extension testing, catheter-based blood pressure, and wire myography, yielding the time evolution of arterial thickening, stiffening, and vasoactive dysfunction required to fit G&R constitutive parameters. Results: Excellent agreement was observed between model predictions and observed patterns of arterial thickening, stiffening, and dysfunction among all CoA groups. For example, predicted vascular impairment was not significantly different from empirical observations via wire myography (p-value > 0.13). Specifically, 48% and 45% impairment was observed in smooth muscle contraction and endothelial-dependent relaxation, respectively, which were accurately predicted using the G&R model. Conclusions: The resulting G&R model, for the first time, allows for prediction of hypertension precursors at neonatal ages that is currently challenging to examine in preclinical models. These findings provide a validated computational tool for prediction of persistent arterial dysfunction and identification of revised severity–duration thresholds that may ultimately avoid hypertension from CoA.

Funder

NIH

Publisher

MDPI AG

Subject

General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)

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