Fluid–structure interaction models of the mitral valve: function in normal and pathological states

• Published in: Philosophical transactions of the Royal Society of London. Series B. Biological sciences 2007-08, Vol.362 (1484), p.1393-1406
• Main Authors: Kunzelman, K.S, Einstein, D.R, Cochran, R.P
• Format: Article
• Language: English
• Subjects: Algorithms; Anisotropy; Biomechanical Phenomena; Blood Circulation; Collagen - physiology; Collagens; Computer analysis; Computer Model; Computer Simulation; Elastic Tissue; Fluid Flow; FSI model; Heart valves; Material concentration; Mitral Valve; Mitral Valve - pathology; Mitral Valve - physiology; Modeling; Models, Biological; Papillary muscles; Pathology; Stiffness
• ISSN: 0962-8436; 1471-2970
• DOI: 10.1098/rstb.2007.2123

Successful mitral valve repair is dependent upon a full understanding of normal and abnormal mitral valve anatomy and function. Computational analysis is one such method that can be applied to simulate mitral valve function in order to analyse the roles of individual components and evaluate proposed surgical repair. We developed the first three-dimensional finite element computer model of the mitral valve including leaflets and chordae tendineae; however, one critical aspect that has been missing until the last few years was the evaluation of fluid flow, as coupled to the function of the mitral valve structure. We present here our latest results for normal function and specific pathological changes using a fluid-structure interaction model. Normal valve function was first assessed, followed by pathological material changes in collagen fibre volume fraction, fibre stiffness, fibre splay and isotropic stiffness. Leaflet and chordal stress and strain and papillary muscle force were determined. In addition, transmitral flow, time to leaflet closure and heart valve sound were assessed. Model predictions in the normal state agreed well with a wide range of available in vivo and in vitro data. Further, pathological material changes that preserved the anisotropy of the valve leaflets were found to preserve valve function. By contrast, material changes that altered the anisotropy of the valve were found to profoundly alter valve function. The addition of blood flow and an experimentally driven microstructural description of mitral tissue represent significant advances in computational studies of the mitral valve, which allow further insight to be gained. This work is another building block in the foundation of a computational framework to aid in the refinement and development of a truly non-invasive diagnostic evaluation of the mitral valve. Ultimately, it represents the basis for simulation of surgical repair of pathological valves in a clinical and educational setting.