Abstract

Plaque rupture is the critical cause of cardiovascular thrombosis, but the detailed mechanisms are not fully understood. Recent studies have found abundant cholesterol crystals in ruptured plaques, and it has been proposed that the rapid expansion of cholesterol crystals in a limited space during crystallization may contribute to plaque rupture. To evaluate the effect of cholesterol crystal growth on atherosclerotic plaques, we modeled the expansion of cholesterol crystals during the crystallization process in the necrotic core and estimated the stress on the thin cap with different arrangements of cholesterol crystals. We developed a two-dimensional finite element method model of atherosclerotic plaques containing expanding cholesterol crystals and investigated the effect of the magnitude and distribution of crystallization on the peak circumferential stress born by the cap. Using micro-optical coherence tomography (μOCT), we extracted the cross-sectional geometric information of cholesterol crystals in human atherosclerotic aorta tissue ex vivo and applied the information to the model. The results demonstrate that (1) the peak circumference stress is proportionally dependent on the cholesterol crystal growth; (2) cholesterol crystals at the cap shoulder impose the highest peak circumference stress; and (3) spatial distributions of cholesterol crystals have a significant impact on the peak circumference stress: evenly distributed cholesterol crystals exert less peak circumferential stress on the cap than concentrated crystals.

Highlights

  • The common morphometric characteristic of a vulnerable plaque is a thin fibrous cap overlying an extensive lipid-rich necrotic core [1,2,3,4]

  • To quantitatively characterize the effects of cholesterol crystal growth on peak circumferential stress (PCS), we investigated the PCS changes caused by their expansion and spatial distributions

  • We found that the loading of concentrated crystals at the cap shoulder imposed the highest risk of plaque rupture by proportionally increasing PCS, whereas the evenly distributed crystal loading along the cap mitigated this risk by exerting less PCS than concentrated crystals

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Summary

Introduction

The common morphometric characteristic of a vulnerable plaque is a thin fibrous cap overlying an extensive lipid-rich necrotic core [1,2,3,4]. Recent studies by Abela et al have indicated that cholesterol crystals may play a significant role in plaque rupture. The crystallization of cholesterol in an atheromatous plaque leads to the rapid accumulation of these crystals in a limited space. The crystals extrude through or protrude into membranes, damaging the fibrous cap and increasing the potential of plaque rupture [5,6,7]. This proposal is supported by PLOS ONE | DOI:10.1371/journal.pone.0155117. This proposal is supported by PLOS ONE | DOI:10.1371/journal.pone.0155117 May 5, 2016

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