人口统计学和危险因素对人股腘动脉非线性正交各向异性力学特性的差异影响。

IF 2.7 3区 医学 Q2 BIOPHYSICS
Majid Jadidi, Sayed Ahmadreza Razian, Alireza Zarreh, Ramin Shahbad, Alexey Kamenskiy
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引用次数: 0

摘要

了解人口统计学和危险因素如何影响人类股腘动脉(fpa)的非线性正交各向异性力学特性,对于改进设备-动脉相互作用的计算模型至关重要。然而,直接评估这些影响是具有挑战性的,因为它们之间错综复杂的相互关系和对动脉力学的多方面影响。本研究旨在利用机器学习(ML)量化衰老、糖尿病、肥胖、高血压和冠状动脉疾病对人类fpa机械行为的独立和联合影响。对450例12 ~ 99岁的组织供体(平均年龄51±18岁,男性占66%)的fpa进行多比值平面双轴扩展。通过超参数调整和交叉验证优化的ML模型用于描述基于人口统计学和危险因素的受试者特定非线性正交异性动脉特性。年龄占动脉力学变异性的60%,纵向比周向的影响更大。糖尿病和冠状动脉疾病的存在分别使血管年龄增加13岁和11岁
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differential effects of demographics and risk factors on the nonlinear orthotropic mechanical properties of human femoropopliteal arteries

Understanding how demographics and risk factors differentially affect the nonlinear orthotropic mechanical properties of human femoropopliteal arteries (FPAs) is critical for improving computational models of device–artery interactions. However, directly assessing these effects is challenging due to their intricate interrelationships and multifaceted impact on arterial mechanics. This study aimed to quantify the independent and combined effects of aging, diabetes, obesity, hypertension, and coronary artery disease on the mechanical behavior of human FPAs using machine learning (ML). FPAs from 450 tissue donors 12–99 years old (average age 51 ± 18 years, 66% male) were evaluated using multi-ratio planar biaxial extension. ML models, optimized through hyperparameter tuning and cross-validation, were used to describe subject-specific nonlinear orthotropic arterial properties based on demographics and risk factors. Age accounted for 60% of the variability in arterial mechanics and had a stronger influence longitudinally than circumferentially. The presence of diabetes and coronary artery disease each added 13 and 11 years to vascular age circumferentially but < 3 years longitudinally. Obesity and hypertension each added 4 years to vascular age circumferentially and less than 3 years longitudinally. Compound effects of diabetes, hypertension, and obesity aged the artery more than 21 years circumferentially and 7 years longitudinally. These findings highlight the differential impact of risk factors on orthotropic arterial mechanics and demonstrate the potential of our approach for predicting subject-specific vascular properties. Incorporating these findings into computational models can enhance the accuracy of device–artery interaction simulations by accounting for individual-specific vascular characteristics.

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来源期刊
Biomechanics and Modeling in Mechanobiology
Biomechanics and Modeling in Mechanobiology 工程技术-工程:生物医学
CiteScore
7.10
自引率
8.60%
发文量
119
审稿时长
6 months
期刊介绍: Mechanics regulates biological processes at the molecular, cellular, tissue, organ, and organism levels. A goal of this journal is to promote basic and applied research that integrates the expanding knowledge-bases in the allied fields of biomechanics and mechanobiology. Approaches may be experimental, theoretical, or computational; they may address phenomena at the nano, micro, or macrolevels. Of particular interest are investigations that (1) quantify the mechanical environment in which cells and matrix function in health, disease, or injury, (2) identify and quantify mechanosensitive responses and their mechanisms, (3) detail inter-relations between mechanics and biological processes such as growth, remodeling, adaptation, and repair, and (4) report discoveries that advance therapeutic and diagnostic procedures. Especially encouraged are analytical and computational models based on solid mechanics, fluid mechanics, or thermomechanics, and their interactions; also encouraged are reports of new experimental methods that expand measurement capabilities and new mathematical methods that facilitate analysis.
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