Automated Segmentation of Microvessels in Intravascular OCT Images Using Deep Learning
FOS: Computer and information sciences
0301 basic medicine
Technology
Computer Science - Machine Learning
optical coherence tomography
QH301-705.5
T
Computer Vision and Pattern Recognition (cs.CV)
segmentation
Image and Video Processing (eess.IV)
Computer Science - Computer Vision and Pattern Recognition
deep learning
Electrical Engineering and Systems Science - Image and Video Processing
Article
Machine Learning (cs.LG)
03 medical and health sciences
0302 clinical medicine
classification
optical coherence tomography; microvessel; deep learning; segmentation; classification
microvessel
FOS: Electrical engineering, electronic engineering, information engineering
Biology (General)
DOI:
10.3390/bioengineering9110648
Publication Date:
2022-11-04T07:28:10Z
AUTHORS (13)
ABSTRACT
Microvessels in vascular plaque are associated with plaque progression and are found in plaque rupture and intra-plaque hemorrhage. To analyze this characteristic of vulnerability, we developed an automated deep learning method for detecting microvessels in intravascular optical coherence tomography (IVOCT) images. A total of 8403 IVOCT image frames from 85 lesions and 37 normal segments were analyzed. Manual annotation was performed using a dedicated software (OCTOPUS) previously developed by our group. Data augmentation in the polar (r,θ) domain was applied to raw IVOCT images to ensure that microvessels appear at all possible angles. Pre-processing methods included guidewire/shadow detection, lumen segmentation, pixel shifting, and noise reduction. DeepLab v3+ was used to segment microvessel candidates. A bounding box on each candidate was classified as either microvessel or non-microvessel using a shallow convolutional neural network. For better classification, we used data augmentation (i.e., angle rotation) on bounding boxes with a microvessel during network training. Data augmentation and pre-processing steps improved microvessel segmentation performance significantly, yielding a method with Dice of 0.71 ± 0.10 and pixel-wise sensitivity/specificity of 87.7 ± 6.6%/99.8 ± 0.1%. The network for classifying microvessels from candidates performed exceptionally well, with sensitivity of 99.5 ± 0.3%, specificity of 98.8 ± 1.0%, and accuracy of 99.1 ± 0.5%. The classification step eliminated the majority of residual false positives and the Dice coefficient increased from 0.71 to 0.73. In addition, our method produced 698 image frames with microvessels present, compared with 730 from manual analysis, representing a 4.4% difference. When compared with the manual method, the automated method improved microvessel continuity, implying improved segmentation performance. The method will be useful for research purposes as well as potential future treatment planning.
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CITATIONS (13)
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