TY - JOUR
T1 - The viscoelastic characteristics of in-vitro carotid plaque by Kelvin-Voigt fractional derivative modeling
AU - Zhou, Yan
AU - Song, Yan
AU - Liu, Zhihui
AU - Li, Wenbin
AU - Guo, Ying
AU - Matkovic, Luke A.
AU - Yang, Xiaofeng
AU - Ma, Ruining
AU - Wan, Mingxi
AU - Ruan, Litao
AU - Zhang, Hongmei
N1 - Publisher Copyright:
© 2022 Elsevier Ltd
PY - 2022/8
Y1 - 2022/8
N2 - Atherosclerotic plaque with a thin fibrous cap can be ruptured by shear force. Exploiting the mechanical properties of plaques within different histological regions can help to better understand the physical mechanisms of the plaque. The association between the plaque components and viscoelasticity was studied when mapping the viscoelasticity to histological features. Eleven in-vitro carotid plaques were tested with ramp-hold relaxation nanoindentation tests. Viscoelasticity (elastic modulus E0, fluidity α, and viscosity τ) was characterized by Kelvin-Voigt fractional derivative (KVFD) modeling. There is a significant difference (p < 0.001) on E0, α, and τ between the collagen-rich (CR) group and the non-collagen-rich (NCR) group. In the CR group, the elastic modulus E0 was higher but the fluidity α and viscosity τ were lower than those of the NCR group. Receiver operating characteristic (ROC) analysis revealed that combinations of E0 and α can be used as a CR indicator with an area under the curve (AUC) of 0.770. There was a negative correlation between E0 and the percentages of myxoid degeneration (r = −0.160, p < 0.001), necrosis (r = −0.229, p < 0.001) and inflammatory cells (r = −0.130, p < 0.001), and a positive correlation between elasticity E0 and the percentage of foam cells (r = 0.121, p < 0.001). There was a positive correlation between fluidity α and the percentage of necrosis (r = 0.308, p < 0.001). The results confirmed the clinical evidence that the CR group with higher elasticity and lower fluidity has higher resisting ability, whereas the NCR group with lower elasticity and higher fluidity has accompanied with more myxoid degeneration, extracellular lipids and necrosis.
AB - Atherosclerotic plaque with a thin fibrous cap can be ruptured by shear force. Exploiting the mechanical properties of plaques within different histological regions can help to better understand the physical mechanisms of the plaque. The association between the plaque components and viscoelasticity was studied when mapping the viscoelasticity to histological features. Eleven in-vitro carotid plaques were tested with ramp-hold relaxation nanoindentation tests. Viscoelasticity (elastic modulus E0, fluidity α, and viscosity τ) was characterized by Kelvin-Voigt fractional derivative (KVFD) modeling. There is a significant difference (p < 0.001) on E0, α, and τ between the collagen-rich (CR) group and the non-collagen-rich (NCR) group. In the CR group, the elastic modulus E0 was higher but the fluidity α and viscosity τ were lower than those of the NCR group. Receiver operating characteristic (ROC) analysis revealed that combinations of E0 and α can be used as a CR indicator with an area under the curve (AUC) of 0.770. There was a negative correlation between E0 and the percentages of myxoid degeneration (r = −0.160, p < 0.001), necrosis (r = −0.229, p < 0.001) and inflammatory cells (r = −0.130, p < 0.001), and a positive correlation between elasticity E0 and the percentage of foam cells (r = 0.121, p < 0.001). There was a positive correlation between fluidity α and the percentage of necrosis (r = 0.308, p < 0.001). The results confirmed the clinical evidence that the CR group with higher elasticity and lower fluidity has higher resisting ability, whereas the NCR group with lower elasticity and higher fluidity has accompanied with more myxoid degeneration, extracellular lipids and necrosis.
KW - Carotid plaque
KW - Kelvin-Voigt fractional derivative (KVFD) model
KW - Risk of vulnerability
KW - Viscoelastic measurement
UR - https://www.scopus.com/pages/publications/85133231107
U2 - 10.1016/j.jbiomech.2022.111210
DO - 10.1016/j.jbiomech.2022.111210
M3 - 文章
C2 - 35785652
AN - SCOPUS:85133231107
SN - 0021-9290
VL - 141
JO - Journal of Biomechanics
JF - Journal of Biomechanics
M1 - 111210
ER -