TY - JOUR
T1 - Higher critical plaque wall stress in patients who died of coronary artery disease compared with those who died of other causes
T2 - A 3D FSI study based on ex vivo MRI of coronary plaques
AU - Huang, Xueying
AU - Yang, Chun
AU - Zheng, Jie
AU - Bach, Richard
AU - Muccigrosso, David
AU - Woodard, Pamela K.
AU - Tang, Dalin
N1 - Funding Information:
This research was supported in part by NSF Grant DMS-0540684 and NIH Grant R01 EB004759 . Dr. Xueying Huang's research was partially supported by the National Natural Science Foundation of China (Grant no. 31100670 ), Natural Science Foundation of Fujian Province of China (Grant no. 2011J05008 ), and Fundamental Research Funds for the Central Universities (Grant no. 2012121003 ). Professor Chun Yang's research was supported in part by the National Natural Sciences Foundation of China (Grant no. 11171030 ).
PY - 2014/1/22
Y1 - 2014/1/22
N2 - Mechanical forces play an important role in the rupture of vulnerable plaques. This process is often associated with cardiovascular syndromes, such as heart attack and stroke. In this study, magnetic resonance imaging (MRI)-based models were used to investigate the association between plaque wall stress (PWS) and coronary artery disease (CAD).Ex vivo MRI data of coronary plaques from 12 patients were used to construct 12 three-dimensional (3D) fluid-structure interaction (FSI) computational models. Six of the patients had died from CAD and six had died from non-CAD causes. PWS was assessed using all nodal points on the lumen surface of each plaque. The maximum PWS from all possible vulnerable sites of each plaque was defined as the 3D critical plaque wall stress (CPWS).Mean 3D CPWS in the CAD group was 94.3% higher than that in the non-CAD group (265.6 vs. 136.7. kPa, P=0.0029). There was no statistically significant difference in global maximum plaque wall stress (GMPWS) between the two groups (P=0.347). There was also no statistically significant difference in plaque burden between the CAD group (84.4±5%) and the non-CAD group (82.0±8%, P=0.552). The results indicate that plaques from patients who died from CAD were associated with higher CPWS compared with those from patients who died from non-CAD causes. With further validation, analysis of CPWS may prove to be an important component in assessment of plaque vulnerability.
AB - Mechanical forces play an important role in the rupture of vulnerable plaques. This process is often associated with cardiovascular syndromes, such as heart attack and stroke. In this study, magnetic resonance imaging (MRI)-based models were used to investigate the association between plaque wall stress (PWS) and coronary artery disease (CAD).Ex vivo MRI data of coronary plaques from 12 patients were used to construct 12 three-dimensional (3D) fluid-structure interaction (FSI) computational models. Six of the patients had died from CAD and six had died from non-CAD causes. PWS was assessed using all nodal points on the lumen surface of each plaque. The maximum PWS from all possible vulnerable sites of each plaque was defined as the 3D critical plaque wall stress (CPWS).Mean 3D CPWS in the CAD group was 94.3% higher than that in the non-CAD group (265.6 vs. 136.7. kPa, P=0.0029). There was no statistically significant difference in global maximum plaque wall stress (GMPWS) between the two groups (P=0.347). There was also no statistically significant difference in plaque burden between the CAD group (84.4±5%) and the non-CAD group (82.0±8%, P=0.552). The results indicate that plaques from patients who died from CAD were associated with higher CPWS compared with those from patients who died from non-CAD causes. With further validation, analysis of CPWS may prove to be an important component in assessment of plaque vulnerability.
KW - Coronary artery disease
KW - Fluid structure interactions
KW - Magnetic resonance imaging
KW - Stress
KW - Vulnerable plaque
UR - http://www.scopus.com/inward/record.url?scp=84891824575&partnerID=8YFLogxK
U2 - 10.1016/j.jbiomech.2013.11.007
DO - 10.1016/j.jbiomech.2013.11.007
M3 - Article
C2 - 24345380
AN - SCOPUS:84891824575
SN - 0021-9290
VL - 47
SP - 432
EP - 437
JO - Journal of Biomechanics
JF - Journal of Biomechanics
IS - 2
ER -