Ventricle Stress/Strain Comparison Between Models Using Different Zero-Load Diastole and Systole Morphologies and Models Using Only One Zero-Load Morphologies

Q4 Biochemistry, Genetics and Molecular Biology Molecular & Cellular Biomechanics Pub Date : 2019-02-21 DOI:10.32604/MCB.2019.05837
Han Yu, P. J. Nido, T. Geva, Chun Yang, Zheyang Wu, R. Rathod, Xueying Huang, K. Billiar, D. Tang
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引用次数: 1

Abstract

Ventricle mechanical stress and strain calculations play an important role in cardiovascular investigations. Patients with repaired tetralogy of Fallot (TOF) account for the majority of cases with late onset right ventricular (RV) failure. The current surgical approach, including pulmonary valve replacement(PVR), has yielded mixed results with some patients recover RV function after pulmonary valve insertion with or without concomitant RV remodeling surgery but some do not[Therrien, Siu and McLaughlin (2000);]. Cardiac magnetic resonance (CMR) data were collected from 6 healthy volunteers and 12 Tetralogy of Fallot (TOF) patients before PVR with consent obtained. 12 patients were divided into two groups depending on right ventricle post-surgery recover( 6 for each group). 3D patient-specific CMR-based ventricle models with different zero-load diastole and systole geometries were constructed to qualify right ventricle (RV) stress and strain values at begin-filling, end-filling, begin-ejection, and end-ejection, respectively. The models are solved with ADINA. Our new models (called 2G models) could provide end-diastole and end-systole stress/strain values which the old models with only one zero-load geometries (called 1G models) could not provide[Tang, Del Nido, Yang, et al., 2016]. Logistic regression with 5-fold cross validation was adopted to predict pulmonary valve replacement outcome.  The results showed 2G mean end-ejection stress value from the 18 participants was 321.4% higher than that from 1G models (p=0.0002). 2G mean strain values was 230% higher than that of 1G models (p=0.0002). TOF group (TG) end-ejection mean stress value was 105.4% higher than that of healthy group (HG) (17.54±7.42kPa vs. 8.54±0.92kPa, p=0.0245).  Worse outcome group (WG) begin-ejection mean stress was 57.4% higher than that of better outcome group (BG, 86.94±26.29 vs. 52.93±22.86 kPa; p=0.041). Among 7 chosen parameters (stress, strain, age, gender, right volume end-diastole volume index, right volume end-systole volume index and ejection fracture), end-filling stress was the best predictor to differentiate BG patients from WG patients with prediction accuracy = 0.8208.  2G models may provide more accurate stress/strain results than 1G models and be applied in clinical situation, potentially.  Large scale studies are still needed for validation.
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不同零负荷舒张和收缩形态模型与单一零负荷形态模型心室应力/应变比较
心室机械应力和应变计算在心血管研究中起着重要作用。修复性法洛四联症(TOF)患者占晚发型右心室(RV)衰竭病例的大多数。目前的手术方法,包括肺动脉瓣置换术(PVR),产生了不同的结果,一些患者在肺动脉瓣置入后恢复了右心室功能,并伴有或不伴有右心室重塑手术,但有些患者没有[Therrien, Siu和McLaughlin(2000)]。6名健康志愿者和12名法洛四联症(TOF)患者经同意后,在PVR前采集心脏磁共振(CMR)数据。12例患者根据术后右心室恢复情况分为两组(每组6例)。构建具有不同零负荷舒张和收缩几何形状的三维患者cmr心室模型,分别在填充开始、填充结束、弹射开始和弹射结束时确定右心室(RV)的应力和应变值。用ADINA对模型进行求解。我们的新模型(称为2G模型)可以提供只有一个零载荷几何形状的旧模型(称为1G模型)无法提供的舒张末期和收缩末期应力/应变值[Tang, Del Nido, Yang等,2016]。采用五重交叉验证的Logistic回归预测肺瓣膜置换术的预后。结果显示,18名参与者的2G平均弹射应力值比1G模型高321.4% (p=0.0002)。2G平均应变值比1G模型高230% (p=0.0002)。TOF组(TG)射血终末平均应激值较健康组(HG)高105.4%(17.54±7.42kPa vs. 8.54±0.92kPa, p=0.0245)。结果较差组(WG)开始射血平均应激比结果较好组(BG, 86.94±26.29 vs 52.93±22.86 kPa)高57.4%;p = 0.041)。在选取的7个参数(应力、应变、年龄、性别、右容积舒张末期容积指数、右容积收缩末期容积指数、射血骨折)中,充盈末期应力是区分BG和WG患者的最佳预测指标,预测准确率为0.8208。2G模型可能比1G模型提供更准确的应力/应变结果,有应用于临床的潜力。仍然需要大规模的研究来验证。
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来源期刊
Molecular & Cellular Biomechanics
Molecular & Cellular Biomechanics CELL BIOLOGYENGINEERING, BIOMEDICAL&-ENGINEERING, BIOMEDICAL
CiteScore
1.70
自引率
0.00%
发文量
21
期刊介绍: The field of biomechanics concerns with motion, deformation, and forces in biological systems. With the explosive progress in molecular biology, genomic engineering, bioimaging, and nanotechnology, there will be an ever-increasing generation of knowledge and information concerning the mechanobiology of genes, proteins, cells, tissues, and organs. Such information will bring new diagnostic tools, new therapeutic approaches, and new knowledge on ourselves and our interactions with our environment. It becomes apparent that biomechanics focusing on molecules, cells as well as tissues and organs is an important aspect of modern biomedical sciences. The aims of this journal are to facilitate the studies of the mechanics of biomolecules (including proteins, genes, cytoskeletons, etc.), cells (and their interactions with extracellular matrix), tissues and organs, the development of relevant advanced mathematical methods, and the discovery of biological secrets. As science concerns only with relative truth, we seek ideas that are state-of-the-art, which may be controversial, but stimulate and promote new ideas, new techniques, and new applications.
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