多模态深度梗塞:利用硅内-人类复合数据学习无创识别梗死心肌。

Rana Raza Mehdi, Nikhil Kadivar, Tanmay Mukherjee, Emilio A Mendiola, Dipan J Shah, George Karniadakis, Reza Avazmohammadi
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摘要

心肌梗死(MI)仍然是全球死亡的主要原因。梗死组织的精确定量对于诊断、治疗管理和心肌梗死后的护理至关重要。晚期钆增强-心脏磁共振成像(LGE-CMR)被认为是精确定位心肌梗死患者梗死组织的黄金标准。LGE-CMR 的一个基本局限是需要通过侵入性静脉注射钆基造影剂,而钆基造影剂具有潜在的高风险毒性,尤其是对患有慢性肾脏疾病的患者而言。在此,我们开发了一种完全无创的方法,通过机器学习(ML)模型,仅使用心脏应变作为输入,就能确定左心室梗死区域的位置和范围。在这一变革性方法中,我们展示了多保真度 ML 模型的卓越性能,该模型结合了基于啮齿动物硅胶内生成的训练数据(低保真度)和非常有限的患者特异性人类数据(高保真度),用于预测 LGE 地面真值。我们的研究结果为开发可行的预后工具提供了一种新的范例,即通过极少量的活体人体数据来增强基于合成模拟的数据。更广泛地说,所提出的方法可以极大地帮助解决人类数据有限的医疗保健领域的生物医学难题。
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Multi-Modality Deep Infarct: Non-invasive identification of infarcted myocardium using composite in-silico-human data learning.

Myocardial infarction (MI) continues to be a leading cause of death worldwide. The precise quantification of infarcted tissue is crucial to diagnosis, therapeutic management, and post-MI care. Late gadolinium enhancement-cardiac magnetic resonance (LGE-CMR) is regarded as the gold standard for precise infarct tissue localization in MI patients. A fundamental limitation of LGE-CMR is the invasive intravenous introduction of gadolinium-based contrast agents that present potential high-risk toxicity, particularly for individuals with underlying chronic kidney diseases. Herein, we develop a completely non-invasive methodology that identifies the location and extent of an infarct region in the left ventricle via a machine learning (ML) model using only cardiac strains as inputs. In this transformative approach, we demonstrate the remarkable performance of a multi-fidelity ML model that combines rodent-based in-silico-generated training data (low-fidelity) with very limited patient-specific human data (high-fidelity) in predicting LGE ground truth. Our results offer a new paradigm for developing feasible prognostic tools by augmenting synthetic simulation-based data with very small amounts of in-vivo human data. More broadly, the proposed approach can significantly assist with addressing biomedical challenges in healthcare where human data are limited.

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