Machine learning‐directed electrical impedance tomography to predict metabolically vulnerable plaques

Author:

Chen Justin1ORCID,Wang Shaolei1,Wang Kaidong2,Abiri Parinaz12,Huang Zi‐Yu3,Yin Junyi1,Jabalera Alejandro M.1,Arianpour Brian1,Roustaei Mehrdad1,Zhu Enbo2,Zhao Peng2,Cavallero Susana24,Duarte‐Vogel Sandra5,Stark Elena6,Luo Yuan3,Benharash Peyman7,Tai Yu‐Chong3,Cui Qingyu2,Hsiai Tzung K.1234

Affiliation:

1. Department of Bioengineering, Henry Samueli School of Engineering University of California, Los Angeles Los Angeles California USA

2. Division of Cardiology, Department of Medicine, David Geffen School of Medicine University of California, Los Angeles Los Angeles California USA

3. Department of Medical Engineering California Institute of Technology Pasadena California USA

4. Division of Cardiology, Department of Medicine Greater Los Angeles VA Healthcare System Los Angeles California USA

5. Division of Laboratory Animal Medicine, David Geffen School of Medicine University of California, Los Angeles Los Angeles California USA

6. Division of Anatomy, Department of Pathology and Laboratory Medicine, David Geffen School of Medicine University of California, Los Angeles Los Angeles California USA

7. Division of Cardiothoracic Surgery, Department of Surgery, David Geffen School of Medicine University of California, Los Angeles Los Angeles California USA

Abstract

AbstractThe characterization of atherosclerotic plaques to predict their vulnerability to rupture remains a diagnostic challenge. Despite existing imaging modalities, none have proven their abilities to identify metabolically active oxidized low‐density lipoprotein (oxLDL), a marker of plaque vulnerability. To this end, we developed a machine learning‐directed electrochemical impedance spectroscopy (EIS) platform to analyze oxLDL‐rich plaques, with immunohistology serving as the ground truth. We fabricated the EIS sensor by affixing a six‐point microelectrode configuration onto a silicone balloon catheter and electroplating the surface with platinum black (PtB) to improve the charge transfer efficiency at the electrochemical interface. To demonstrate clinical translation, we deployed the EIS sensor to the coronary arteries of an explanted human heart from a patient undergoing heart transplant and interrogated the atherosclerotic lesions to reconstruct the 3D EIS profiles of oxLDL‐rich atherosclerotic plaques in both right coronary and left descending coronary arteries. To establish effective generalization of our methods, we repeated the reconstruction and training process on the common carotid arteries of an unembalmed human cadaver specimen. Our findings indicated that our DenseNet model achieves the most reliable predictions for metabolically vulnerable plaque, yielding an accuracy of 92.59% after 100 epochs of training.

Funder

National Institutes of Health

National Institute of General Medical Sciences

VA Greater Los Angeles Healthcare System

Publisher

Wiley

Subject

Pharmaceutical Science,Biomedical Engineering,Biotechnology

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