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Stroke Lesion Segmentation in FLAIR MRI Datasets Using Customized Markov Random Fields.

Nagesh K Subbanna1, Deepthi Rajashekar1, Bastian Cheng2

  • 1Department of Radiology, University of Calgary, Calgary, AB, Canada.

Frontiers in Neurology
|June 11, 2019
PubMed
Summary
This summary is machine-generated.

This study introduces a novel Bayesian method for segmenting sub-acute ischemic stroke lesions using only FLAIR MRI. The technique achieves robust segmentation, outperforming existing methods and aiding clinical trial endpoint analysis.

Keywords:
brain lesion segmentationclassificationimage segmentationischemic strokemagnetic resonance imaging

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Area of Science:

  • Medical Imaging
  • Computational Neuroscience
  • Radiology

Background:

  • Accurate segmentation of stroke lesions is vital for using lesion volume as a clinical trial endpoint.
  • Current segmentation methods often require multi-modal Magnetic Resonance Imaging (MRI) data.

Purpose of the Study:

  • To develop and evaluate a novel method for segmenting sub-acute ischemic stroke lesions using only Fluid-Attenuated Inversion Recovery (FLAIR) MRI.
  • To assess the robustness and reliability of the proposed segmentation technique.

Main Methods:

  • A Bayesian technique utilizing Gabor textures from FLAIR signal intensities for initial segmentation.
  • A customized voxel-level Markov Random Field model incorporating intensity and Gabor texture features for refinement.
  • Validation on 151 multi-center datasets using a leave-one-patient-out approach.

Main Results:

  • Achieved an average Dice coefficient of 0.582, competitive with multi-modal MRI methods.
  • Demonstrated superior performance compared to leading Convolutional Neural Network and level-set methods from the ISLES 2015 challenge.
  • The method provides robust lesion segmentation using only FLAIR MRI sequences.

Conclusions:

  • The proposed method offers a reliable and robust approach for segmenting sub-acute ischemic stroke lesions from FLAIR MRI.
  • This technique has the potential to serve as a valuable tool in clinical trials, particularly as a follow-up sequence analysis.