4.5 Article

Automated A-line coronary plaque classification of intravascular optical coherence tomography images using handcrafted features and large datasets

期刊

JOURNAL OF BIOMEDICAL OPTICS
卷 24, 期 10, 页码 -

出版社

SPIE-SOC PHOTO-OPTICAL INSTRUMENTATION ENGINEERS
DOI: 10.1117/1.JBO.24.10.106002

关键词

machine learning; intravascular optical coherence tomography; cryo-imaging

资金

  1. National Heart, Lung, and Blood Institute through the U.S. National Institutes of Health (NIH) [R21HL108263, R01HL143484, R01HL114406]
  2. NIH Construction Grant [C06 RR12463]
  3. Choose Ohio First Scholarship
  4. Case Western Reserve University
  5. University Hospitals of Cleveland

向作者/读者索取更多资源

We developed machine learning methods to identify fibrolipidic and fibrocalcific A-lines in intravascular optical coherence tomography (IVOCT) images using a comprehensive set of handcrafted features. We incorporated features developed in previous studies (e.g., optical attenuation and A-line peaks). In addition, we included vascular lumen morphology and three-dimensional (3-D) digital edge and texture features. Classification methods were developed using expansive datasets (similar to 7000 images), consisting of both clinical in vivo images and an ex vivo dataset, which was validated using 3-D cryo-imaging/histology. Conditional random field was used to perform 3-D classification noise cleaning of classification results. We tested various multiclass approaches, classifiers, and feature selection schemes and found that a three-class support vector machine with minimal-redundancy-maximal-relevance feature selection gave the best performance. We found that inclusion of our morphological and 3-D features improved overall classification accuracy. On a held-out test set consisting of >1700 images, we obtained an overall accuracy of 81.58%, with the following (sensitivity/ specificity) for each class: other (81.43/89.59), fibrolipidic (94.48/87.32), and fibrocalcific (74.82/95.28). The en face views of classification results showed that automated classification easily captured the preponderance of a disease segment (e.g., a calcified segment had large regions of fibrocalcific classifications). Finally, we demonstrated proof-of-concept for streamlining A-line classification output with existing fibrolipidic and fibrocalcific boundary segmentation methods, to enable fully automated plaque quantification. The results suggest that our classification approach is a viable step toward fully automated IVOCT plaque classification and segmentation for live-time treatment planning and for offline assessment of drug and biologic therapeutics. (C) The Authors. Published by SPIE under a Creative Commons Attribution 4.0 Unported License.

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