Phenotyping calcification in vascular tissues using artificial intelligence

Mehdi Ramezanpour, Anne M. Robertson, Yasutaka Tobe, Xiaowei Jia, Juan R. Cebral
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Abstract

Vascular calcification is implicated as an important factor in major adverse cardiovascular events (MACE), including heart attack and stroke. A controversy remains over how to integrate the diverse forms of vascular calcification into clinical risk assessment tools. Even the commonly used calcium score for coronary arteries, which assumes risk scales positively with total calcification, has important inconsistencies. Fundamental studies are needed to determine how risk is influenced by the diverse calcification phenotypes. However, studies of these kinds are hindered by the lack of high-throughput, objective, and non-destructive tools for classifying calcification in imaging data sets. Here, we introduce a new classification system for phenotyping calcification along with a semi-automated, non-destructive pipeline that can distinguish these phenotypes in even atherosclerotic tissues. The pipeline includes a deep-learning-based framework for segmenting lipid pools in noisy micro-CT images and an unsupervised clustering framework for categorizing calcification based on size, clustering, and topology. This approach is illustrated for five vascular specimens, providing phenotyping for thousands of calcification particles across as many as 3200 images in less than seven hours. Average Dice Similarity Coefficients of 0.96 and 0.87 could be achieved for tissue and lipid pool, respectively, with training and validation needed on only 13 images despite the high heterogeneity in these tissues. By introducing an efficient and comprehensive approach to phenotyping calcification, this work enables large-scale studies to identify a more reliable indicator of the risk of cardiovascular events, a leading cause of global mortality and morbidity.
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利用人工智能对血管组织中的钙化进行表型分析
血管钙化是心脏病和中风等心血管重大不良事件(MACE)的重要诱因。如何将不同形式的血管钙化纳入临床风险评估工具仍存在争议。即使是常用的冠状动脉钙化评分(该评分假定风险与总钙化呈正比)也存在严重的不一致性。然而,由于缺乏高通量、客观和非破坏性的工具来对成像数据集中的钙化进行分类,此类研究受到了阻碍。在这里,我们介绍了一种新的钙化表型分类系统,以及一种半自动、非破坏性的管道,它甚至可以区分动脉粥样硬化组织中的这些表型。该管道包括一个基于深度学习的框架,用于分割噪声微 CT 图像中的脂质池;以及一个无监督聚类框架,用于根据大小、聚类和拓扑结构对钙化进行分类。尽管这些组织的异质性很高,但只需在 13 幅图像上进行训练和验证,就能使组织和脂质池的平均骰子相似系数分别达到 0.96 和 0.87。通过引入一种高效、全面的钙化表型方法,这项工作使大规模研究能够确定心血管事件风险的更可靠指标,而心血管事件是全球死亡和发病的主要原因。
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