Hemodynamics affects factor XI/XII anticoagulation efficacy in patient-derived left atrial models

IF 4.9 2区 医学 Q1 COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS
M. Guerrero-Hurtado , M. Garćia-Villalba , A. Gonzalo , E. Durán , P. Martinez-Legazpi , P. Ávila , A.M. Kahn , M.Y. Chen , E. McVeigh , J. Bermejo , J.C. del Álamo , O. Flores
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引用次数: 0

Abstract

Background and Objective:

Atrial fibrillation (AF) is a common arrhythmia that disrupts blood circulation in the left atrium (LA), causing stasis in the left atrial appendage (LAA) and increasing thromboembolic risk. In patients at sufficiently high risk, anticoagulation is indicated. This benefit may be counterbalanced by an increased risk of bleeding. Novel anticoagulants under development, such as factor XI/XII inhibitors, may be associated with a lower bleeding risk. However, their efficacy in preventing thrombosis is not fully understood. We hypothesized that patient-specific flow patterns in the LA and LAA not only influence the risk of thrombosis but also the effectiveness of anticoagulation agents.

Methods:

To test our hypothesis, we simulated blood flow and the intrinsic coagulation pathway in patient-specific LA anatomies with and without factor XI/XII inhibition. We included a heterogeneous cohort of thirteen patients, some in sinus rhythm and others in AF, four of whom had an LAA thrombus or a history of transient ischemic attacks. We used computational fluid dynamics based on 4D CT imaging and a detailed 32-coagulation factor system to run 247 simulations. We analyzed baseline LA flow patterns and evaluated various factor XI/XII inhibition levels. Implementing a novel multi-fidelity coagulation modeling approach accelerated computations by two orders of magnitude, enabling many simulations to be performed.

Results:

The simulations provided spatiotemporally resolved maps of thrombin concentration throughout the LA, showing that it peaks inside the LAA. Coagulation metrics based on peak LAA thrombin dynamics suggested patients could be classified as having no, moderate or high thromboembolic risk. High-risk patients had slower flows and higher residence times in the LAA than those with moderate thromboembolic risk, and they required stronger factor XI/XII inhibition to prevent thrombin growth. These data suggest that the anticoagulation effect was also related to the LAA hemodynamics.

Conclusion:

The methodology outlined in this study has the potential to enable personalized assessments of coagulation risk and to tailor anticoagulation therapy by analyzing flow dynamics in patient-derived LA models, representing a significant step towards advancing the application of digital twins in cardiovascular medicine.
血流动力学影响患者源性左心房模型XI/XII因子抗凝疗效
背景与目的:心房颤动(AF)是一种常见的心律失常,它会破坏左心房(LA)的血液循环,导致左心房附件(LAA)淤滞,增加血栓栓塞的风险。在足够高的风险患者,抗凝是指。这种好处可能会被出血风险的增加所抵消。正在开发的新型抗凝血剂,如因子XI/XII抑制剂,可能与较低的出血风险相关。然而,它们在预防血栓形成方面的功效尚不完全清楚。我们假设,患者在LA和LAA中的特定血流模式不仅影响血栓形成的风险,而且影响抗凝药物的有效性。方法:为了验证我们的假设,我们模拟了有和没有因子XI/XII抑制的患者特异性LA解剖中的血流和内在凝血途径。我们纳入了13例异质队列患者,其中一些为窦性心律,另一些为房颤,其中4例有LAA血栓或短暂性脑缺血发作史。我们使用基于4D CT成像的计算流体力学和详细的32凝血因子系统进行了247次模拟。我们分析了基线LA流动模式,并评估了各种因子XI/XII抑制水平。实现了一种新的多保真度凝固建模方法,将计算速度提高了两个数量级,使许多模拟能够进行。结果:模拟提供了整个LAA的凝血酶浓度的时空分辨图,表明它在LAA内达到峰值。基于LAA峰值凝血酶动力学的凝血指标表明,患者可分为无、中度或高度血栓栓塞风险。与中度血栓栓塞风险患者相比,高危患者在LAA的血流更慢,停留时间更长,需要更强的因子XI/XII抑制来阻止凝血酶生长。这些数据表明,抗凝作用也与LAA血流动力学有关。结论:本研究概述的方法有可能实现凝血风险的个性化评估,并通过分析患者衍生的LA模型中的血流动力学来定制抗凝治疗,这是推进数字双胞胎在心血管医学中的应用的重要一步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Computer methods and programs in biomedicine
Computer methods and programs in biomedicine 工程技术-工程:生物医学
CiteScore
12.30
自引率
6.60%
发文量
601
审稿时长
135 days
期刊介绍: To encourage the development of formal computing methods, and their application in biomedical research and medical practice, by illustration of fundamental principles in biomedical informatics research; to stimulate basic research into application software design; to report the state of research of biomedical information processing projects; to report new computer methodologies applied in biomedical areas; the eventual distribution of demonstrable software to avoid duplication of effort; to provide a forum for discussion and improvement of existing software; to optimize contact between national organizations and regional user groups by promoting an international exchange of information on formal methods, standards and software in biomedicine. Computer Methods and Programs in Biomedicine covers computing methodology and software systems derived from computing science for implementation in all aspects of biomedical research and medical practice. It is designed to serve: biochemists; biologists; geneticists; immunologists; neuroscientists; pharmacologists; toxicologists; clinicians; epidemiologists; psychiatrists; psychologists; cardiologists; chemists; (radio)physicists; computer scientists; programmers and systems analysts; biomedical, clinical, electrical and other engineers; teachers of medical informatics and users of educational software.
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