| Literature DB >> 31409233 |
Javier Escuer1, Miguel A Martínez1,2, Sean McGinty3, Estefanía Peña1,2.
Abstract
The stenting procedure has evolved to become a highly successful technique for the clinical treatment of advanced atherosclerotic lesions in arteries. However, the development of in-stent restenosis remains a key problem. In this work, a novel two-dimensional continuum mathematical model is proposed to describe the complex restenosis process following the insertion of a stent into a coronary artery. The biological species considered to play a key role in restenosis development are growth factors, matrix metalloproteinases, extracellular matrix, smooth muscle cells and endothelial cells. Diffusion-reaction equations are used for modelling the mass balance between species in the arterial wall. Experimental data from the literature have been used in order to estimate model parameters. Moreover, a sensitivity analysis has been performed to study the impact of varying the parameters of the model on the evolution of the biological species. The results demonstrate that this computational model qualitatively captures the key characteristics of the lesion growth and the healing process within an artery subjected to non-physiological mechanical forces. Our results suggest that the arterial wall response is driven by the damage area, smooth muscle cell proliferation and the collagen turnover among other factors.Entities:
Keywords: continuum models; coronary artery; diffusion–reaction equations; in-stent restenosis; restenosis; stent
Mesh:
Year: 2019 PMID: 31409233 PMCID: PMC6731499 DOI: 10.1098/rsif.2019.0313
Source DB: PubMed Journal: J R Soc Interface ISSN: 1742-5662 Impact factor: 4.118