Haemodynamics and wall remodelling of a growing cerebral aneurysm: A computational model

被引:102
作者
Chatziprodromou, I.
Tricoli, A.
Poulikakos, D.
Ventikos, Y.
机构
[1] Univ Oxford, Dept Engn Sci, Fluid & Biocomplex Grp, Oxford OX1 3PJ, England
[2] ETH Zentrum, Swiss Fed Inst Technol, Lab Thermodynam Emerging Technol, CH-8092 Zurich, Switzerland
关键词
cerebral aneurysms; growth model; computational simulation; biological fluid mechanics;
D O I
10.1016/j.jbiomech.2005.12.009
中图分类号
Q6 [生物物理学];
学科分类号
071011 [生物物理学];
摘要
We have developed a computational simulation model for investigating an often postulated hypothesis connected with aneurysm growth. This hypothesis involves a combination of two parallel and interconnected mechanisms: according to the first mechanism, an endothelium-originating and wall shear stress-driven apoptotic behavior of smooth muscle cells, leading to loss of vascular tone is believed to be important to the aneurysm behavior. Vascular tone refers to the degree of constriction experienced by a blood vessel relative to its maximally dilated state. All resistance and capacitance vessels under basal conditions exhibit some degree of smooth muscle contraction that determines the diameter, and hence tone, of the vessel. The second mechanism is connected to the arterial wall remodeling. Remodeling of the arterial wall under constant tension is a biornechanical process of rupture, degradation and reconstruction of the medial elastin and collagen fibers. In order to investigate these two mechanisms within a computationally tractable framework, we devise mechanical analogues that involve three-dimensional haemodynamics, yielding estimates of the wall shear stress and pressure fields and a quasi-steady approach for the apoptosis and remodeling of the wall. These analogues are guided by experimental information for the connection of stimuli to responses at a cellular level, properly averaged over volumes or surfaces. The model predicts aneurysm growth and can attribute specific roles to the two mechanisms involved: the smooth muscle cell-related loss of tone is important to the initiation of aneurysm growth, but cannot account alone for the formation of fully grown sacks; the fiber-related remodeling is pivotal for the latter. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:412 / 426
页数:15
相关论文
共 69 条
[1]
ION CHANNELS AND REGULATION OF INTRACELLULAR CALCIUM IN VASCULAR ENDOTHELIAL-CELLS [J].
ADAMS, DJ ;
BARAKEH, J ;
LASKEY, R ;
VANBREEMEN, C .
FASEB JOURNAL, 1989, 3 (12) :2389-2400
[2]
WALL SHEAR-STRESS RATHER THAN SHEAR RATE REGULATES CYTOPLASMIC CA++ RESPONSES TO FLOW IN VASCULAR ENDOTHELIAL-CELLS [J].
ANDO, J ;
OHTSUKA, A ;
KORENAGA, R ;
KAWAMURA, T ;
KAMIYA, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 190 (03) :716-723
[3]
[Anonymous], AM SOC CIV ENG P 1
[4]
BALLYK PD, 1994, BIORHEOLOGY, V31, P565
[5]
Hemodynamic changes in recurrent intracranial terminal aneurysm after endovascular treatment [J].
Banerjee, RK ;
Gonzalez, CF ;
Cho, YI ;
Picard, L .
ACADEMIC RADIOLOGY, 1996, 3 (03) :202-211
[6]
Bathe K. J., 1976, NUMERICAL METHODS FI
[7]
A MATHEMATICAL-MODEL OF UNSTEADY COLLAPSIBLE TUBE BEHAVIOR [J].
BERTRAM, CD ;
PEDLEY, TJ .
JOURNAL OF BIOMECHANICS, 1982, 15 (01) :39-50
[8]
Computational simulation of intracoronary flow based on real coronary geometry [J].
Boutsianis, E ;
Dave, H ;
Frauenfelder, T ;
Poulikakos, D ;
Wildermuth, S ;
Turina, M ;
Ventikos, Y ;
Zund, G .
EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, 2004, 26 (02) :248-256
[9]
SHEAR-STRESS INDUCED RELEASE OF NITRIC-OXIDE FROM ENDOTHELIAL-CELLS GROWN ON BEADS [J].
BUGA, GM ;
GOLD, ME ;
FUKUTO, JM ;
IGNARRO, LJ .
HYPERTENSION, 1991, 17 (02) :187-193
[10]
Endothelium-dependent, shear-induced vasodilation is rate-sensitive [J].
Butler, PJ ;
Weinbaum, S ;
Chien, S ;
Lemons, DE .
MICROCIRCULATION, 2000, 7 (01) :53-65