4.3 Article

Automated Segmentation of Microvessels in Intravascular OCT Images Using Deep Learning

Journal

BIOENGINEERING-BASEL
Volume 9, Issue 11, Pages -

Publisher

MDPI
DOI: 10.3390/bioengineering9110648

Keywords

optical coherence tomography; microvessel; deep learning; segmentation; classification

Funding

  1. National Heart, Lung, and Blood Institute
  2. American Heart Association [R21 HL108263, R01 HL114406, R01 HL143484, R01 RES219220]
  3. NIH [20POST35210974]
  4. [C06 RR12463]

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This study developed an automated deep learning method for detecting microvessels in intravascular optical coherence tomography (IVOCT) images. The method showed significantly improved microvessel segmentation performance and high classification accuracy. It has important implications for research and potential future treatment planning.
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,theta) 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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