Why the study?
The effects of muscle fiber orientation angles and tilted muscle fibers on left ventricular myocardial behavior and the occurrence of cardiomyopathies were not fully understood.
Computational modeling suggests that tilted muscle fibers in the myocardium increase residual stress, which may contribute to the development of hypertrophied or dilated cardiomyopathies.
Answers are grounded in this paper and cite their sources.
Suggests fiber orientation influences myocardial mechanics; hypothesis-generating for cardiomyopathy mechanisms, no clinical implications yet.
This paper considers the Holzapfel–Ogden (HO) model to examine the behavior of the left ventricle myocardium. At the tissue level, we analyze the contributions of the orientation angle of muscle fibers (MFs) and investigate their effects on the occurrence of certain cardiomyopathies and congenital diseases at the organ level. Knowing the importance of myocardial microstructure on cardiac function, we vary the angle between the direction of collagen sheets and MFs in all layers of the myocardium (from epicardium to endocardium) to model the effects of tilted MFs. Based on the HO model in which the directions of the fibers are orthogonal and using the strain energy of HO, we construct a tensile-compression test and simulate the dynamics of a cubic sample. We recover the authors’ results exhibiting the existence of residual stresses in various directions. Then, we modify the energy of HO slightly to assess the impact of the same stress states on the system with tilted MFs. A numerical tensile-compression test performed on this new cubic sample shows that, in certain directions, the heart tissue is more resistant to shear deformations in some planes than in others. Moreover, it appears that the residual stress is smaller as the angle of orientation of the MFs is small. Furthermore, we observe that the residual stress is greater in the new model compared to the normal HO model. This could affect the heart muscle at the organ level leading to hypertrophied/dilated cardiomyopathy.
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Djoumessi et al. (2022) studied this question.
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