From Heart to Abdominal Aorta: Integrating Multi-Modal Cardiac Imaging Derived Haemodynamic Biomarkers for Abdominal Aortic Aneurysm Risk Stratification, Surveillance, Pre-Operative Assessment and Therapeutic Decision-Making.

IF 3.3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Rafic Ramses, Obiekezie Agu
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引用次数: 0

Abstract

Recent advances in cardiovascular imaging have revolutionized the assessment and management of abdominal aortic aneurysm (AAA) through the integration of sophisticated haemodynamic biomarkers. This comprehensive review evaluates the clinical utility and mechanistic significance of multiple biomarkers in AAA pathogenesis, progression, and treatment outcomes. Advanced cardiac imaging modalities, including four-dimensional magnetic resonance imaging (4D MRI), computational fluid dynamics (CFD), and specialized echocardiography, enable precise quantification of critical haemodynamic parameters. Wall shear stress (WSS) emerges as a fundamental biomarker, with values below 0.4 Pa indicating pathological conditions and increased risk for aneurysm progression. Time-averaged wall shear stress (TAWSS), typically maintaining values above 1.5 Pa in healthy arterial segments, provides crucial information about sustained haemodynamic forces affecting the vessel wall. The oscillatory shear index (OSI), ranging from 0 (unidirectional flow) to 0.5 (purely oscillatory flow), quantifies directional changes in WSS during cardiac cycles. In AAA, elevated OSI values between 0.3 and 0.4 correlate with disturbed flow patterns and accelerated disease progression. The relative residence time (RRT), combining TAWSS and OSI, identifies regions prone to thrombosis, with values exceeding 2-3 Pa-1 indicating increased risk. The endothelial cell activation potential (ECAP), calculated as OSI/TAWSS, serves as an integrated metric for endothelial dysfunction risk, with values above 0.2-0.3 Pa-1 suggesting increased inflammatory activity. Additional biomarkers include the volumetric perivascular characterization index (VPCI), which assesses vessel wall inflammation through perivascular tissue analysis, and pulse wave velocity (PWV), measuring arterial stiffness. Central aortic systolic pressure and the aortic augmentation index provide essential information about cardiovascular load and arterial compliance. Novel parameters such as particle residence time, flow stagnation, and recirculation zones offer detailed insights into local haemodynamics and potential complications. Implementation challenges include the need for specialized equipment, standardized protocols, and expertise in data interpretation. However, the potential for improved patient outcomes through more precise risk stratification and personalized treatment planning justifies continued development and validation of these advanced assessment tools.

从心脏到腹主动脉:整合多模态心脏成像衍生的血流动力学生物标志物,用于腹主动脉瘤风险分层、监测、术前评估和治疗决策。
心血管成像的最新进展通过整合复杂的血流动力学生物标志物,彻底改变了腹主动脉瘤(AAA)的评估和管理。这篇综合综述评估了AAA发病机制、进展和治疗结果中多种生物标志物的临床应用和机制意义。先进的心脏成像模式,包括四维磁共振成像(4D MRI)、计算流体动力学(CFD)和专门的超声心动图,可以精确量化关键的血流动力学参数。壁面剪切应力(WSS)是一个基本的生物标志物,其值低于0.4 Pa表明病变状态和动脉瘤进展的风险增加。时间平均壁剪切应力(TAWSS)通常在健康动脉段维持在1.5 Pa以上,提供了影响血管壁的持续血流动力学力的重要信息。振荡剪切指数(OSI),范围从0(单向流)到0.5(纯振荡流),量化了心脏周期中WSS的方向性变化。在AAA中,0.3 - 0.4之间的OSI值升高与血流模式紊乱和疾病进展加速相关。相对停留时间(RRT)结合TAWSS和OSI可以识别出血栓形成的易发区域,其值超过2-3 Pa-1表明风险增加。内皮细胞激活电位(ECAP)以OSI/TAWSS计算,作为内皮功能障碍风险的综合指标,其值高于0.2-0.3 Pa-1表明炎症活性增加。其他生物标志物包括容积血管周围特征指数(VPCI),通过血管周围组织分析评估血管壁炎症,以及脉搏波速度(PWV),测量动脉硬度。中心主动脉收缩压和主动脉增强指数提供了心血管负荷和动脉顺应性的重要信息。新的参数,如颗粒停留时间,流动停滞和再循环区域,提供了详细的了解局部血流动力学和潜在的并发症。实施方面的挑战包括需要专用设备、标准化协议和数据解释方面的专业知识。然而,通过更精确的风险分层和个性化治疗计划来改善患者预后的潜力证明了继续开发和验证这些先进的评估工具是合理的。
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
Diagnostics
Diagnostics Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
4.70
自引率
8.30%
发文量
2699
审稿时长
19.64 days
期刊介绍: Diagnostics (ISSN 2075-4418) is an international scholarly open access journal on medical diagnostics. It publishes original research articles, reviews, communications and short notes on the research and development of medical diagnostics. There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental and/or methodological details must be provided for research articles.
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