Beyond the root: Geometric characterization for the diagnosis of syndromic heritable thoracic aortic diseases

IF 7 2区 医学 Q1 BIOLOGY Computers in biology and medicine Pub Date : 2024-11-01 DOI:10.1016/j.compbiomed.2024.109176
Pau Romero , Miguel Lozano , Lydia Dux-Santoy , Andrea Guala , Gisela Teixidó-Turà , Rafael Sebastián , Ignacio García-Fernández
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Abstract

Syndromic heritable thoracic aortic diseases (sHTAD), such as Marfan (MFS) or Loeys–Dietz (LDS) syndromes, involve high risk of life threatening aortic events. Diagnosis of syndromic features alone is difficult, and negative genetic tests do not necessarily exclude a genetic or hereditary condition. Periodic 3D imaging of the aorta is recommended in patients with aortic disease. Thus, an imaging-based approach aimed at identifying unique features of aortic geometry can be highly effective for diagnosing sHTAD and assessing risk. In this study, we present a method that can help identify the manifestations of sHTAD by focusing on the entire geometry of the thoracic aorta, rather than only using measurements of dilation of the aortic root. We analyze the geometric phenotype of 97 patients with genetically confirmed sHTAD (79 MF and 18 LDS) and of 45 healthy volunteers, using 3D aorta meshes obtained from phase contrast-enhanced magnetic resonance angiograms computed from 4D flow cardiac magnetic resonance. We build a geometric encoding of the aorta, based on a vessel coordinate system, and use several mathematical models to discriminate between controls and patients with sHTAD: a baseline scenario, based on aortic root dimensions only, a descriptor typically used in sHTAD patients; a low dimensional scenario, with a reduce encoding using principal component analysis; and a high-dimensional scenario, which included the full coefficient representation for geometry encoding, aiming to capture finer geometric details. The results indicate that considering the anatomy of the whole thoracic aorta can improve predictive ability. We achieve precision and sensitivity values over 0.8, with a specificity of over 70% in all the models used, while a single value classifiers (based only on aortic root diameter) demonstrated a trade-off between sensitivity and specificity. Using the mathematical properties of the vessel coordinate system representation, feature importance is mapped onto a set of anatomical traits that are used by the models to do the classification, thus providing interpretability of the results. This analysis indicates that in addition to the diameter of the aortic root, aortic elongation and a narrowing of the descending thoracic aorta may be markers of positive sHTAD.
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超越根部:用于诊断综合遗传性胸主动脉疾病的几何特征。
综合征遗传性胸主动脉疾病(sHTAD),如马凡(MFS)或洛伊-迪茨(LDS)综合征,具有发生危及生命的主动脉事件的高风险。仅凭综合征特征进行诊断是很困难的,基因检测呈阴性并不一定能排除遗传或遗传性疾病。建议主动脉疾病患者定期进行主动脉三维成像检查。因此,旨在识别主动脉几何形状独特特征的成像方法对于诊断 sHTAD 和评估风险非常有效。在这项研究中,我们提出了一种方法,它可以通过关注整个胸主动脉的几何形状,而不仅仅是测量主动脉根部的扩张来帮助识别 sHTAD 的表现。我们利用从相位对比增强磁共振血管造影中获得的三维主动脉网格,分析了 97 名经基因证实的 sHTAD 患者(79 名中频患者和 18 名低频患者)和 45 名健康志愿者的几何表型。我们基于血管坐标系建立了主动脉的几何编码,并使用几种数学模型来区分对照组和 sHTAD 患者:基线方案,仅基于主动脉根部尺寸,这是通常用于 sHTAD 患者的描述符;低维方案,使用主成分分析进行还原编码;高维方案,包括几何编码的全系数表示,旨在捕捉更精细的几何细节。结果表明,考虑整个胸主动脉的解剖结构可以提高预测能力。我们使用的所有模型的精确度和灵敏度值都超过了 0.8,特异性超过了 70%,而单值分类器(仅基于主动脉根部直径)则在灵敏度和特异性之间进行了权衡。利用血管坐标系表示法的数学特性,特征的重要性被映射到一组解剖特征上,这些特征被模型用来进行分类,从而提供了结果的可解释性。这项分析表明,除了主动脉根部的直径外,主动脉伸长和降胸主动脉变窄也可能是 sHTAD 阳性的标志。
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来源期刊
Computers in biology and medicine
Computers in biology and medicine 工程技术-工程:生物医学
CiteScore
11.70
自引率
10.40%
发文量
1086
审稿时长
74 days
期刊介绍: Computers in Biology and Medicine is an international forum for sharing groundbreaking advancements in the use of computers in bioscience and medicine. This journal serves as a medium for communicating essential research, instruction, ideas, and information regarding the rapidly evolving field of computer applications in these domains. By encouraging the exchange of knowledge, we aim to facilitate progress and innovation in the utilization of computers in biology and medicine.
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