Computational modelling of multi-temporal ventricular–vascular interactions during the progression of pulmonary arterial hypertension

Author:

Pourmodheji Reza1ORCID,Jiang Zhenxiang1,Tossas-Betancourt Christopher2,Dorfman Adam L.3,Figueroa C. Alberto24ORCID,Baek Seungik1,Lee Lik-Chuan1

Affiliation:

1. Department of Mechanical Engineering, Michigan State University, East Lansing, MI, USA

2. Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA

3. Department of Pediatrics, University of Michigan, Ann Arbor, MI, USA

4. Department of Surgery, University of Michigan, Ann Arbor, MI, USA

Abstract

A computational framework is developed to consider the concurrent growth and remodelling (G&R) processes occurring in the large pulmonary artery (PA) and right ventricle (RV), as well as ventricular–vascular interactions during the progression of pulmonary arterial hypertension (PAH). This computational framework couples the RV and the proximal PA in a closed-loop circulatory system that operates in a short timescale of a cardiac cycle, and evolves over a long timescale due to G&R processes in the PA and RV. The framework predicts changes in haemodynamics (e.g. 68.2% increase in mean PA pressure), RV geometry (e.g. 38% increase in RV end-diastolic volume) and PA tissue microstructure (e.g. 90% increase in collagen mass) that are consistent with clinical and experimental measurements of PAH. The framework also predicts that a reduction in RV contractility is associated with long-term RV chamber dilation, a common biomarker observed in the late-stage PAH. Sensitivity analyses on the G&R rate constants show that large PA stiffening (both short and long term) is affected by RV remodelling more than the reverse. This framework can serve as a foundation for the future development of a more predictive and comprehensive cardiovascular G&R model with realistic heart and vascular geometries.

Funder

National Science Foundation Graduate Research Fellowship Program

National Heart, Lung, and Blood Institute

American Heart Association

Publisher

The Royal Society

Subject

Biomedical Engineering,Biochemistry,Biomaterials,Bioengineering,Biophysics,Biotechnology

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