A geometric-to-neural cascade for cerebral microbleed detection in susceptibility-weighted MRI

Sam Bogdanov1, Gaurav Rudravaram2, Adam M Saunders2

  • 1Medical Scientist Training Program, Vanderbilt University, Nashville, TN 37240, USA.

Insights

This study introduces an automated pipeline for detecting cerebral microbleeds (CMBs) in brain imaging, significantly reducing false positives and improving accuracy for diagnosing small vessel disease and cerebral amyloid angiopathy.

Area of Science:

  • Neuroimaging
  • Medical Image Analysis
  • Artificial Intelligence in Medicine

Background:

  • Cerebral microbleeds (CMBs) are key imaging biomarkers for cerebral small vessel disease and cerebral amyloid angiopathy (CAA).
  • Automated CMB detection in susceptibility-weighted imaging (SWI) is hindered by mimics like vessel cross-sections, leading to high false-positive rates.
  • Current methods often require complex, time-consuming voxel-wise segmentation, limiting clinical applicability.

Purpose of the Study:

  • To develop and validate a fully automated, three-stage cascade pipeline for accurate CMB detection in SWI.
  • To minimize false positives by employing a novel approach using quality-assurance labels instead of dense segmentation masks.
  • To provide a computationally efficient and clinically relevant tool for CMB analysis.

Main Methods:

  • A three-stage cascade pipeline combining unsupervised candidate generation (Gaussian Mixture Model, anatomical masking, size/sphericity filtering) and two 3D ResNet classifiers.
  • Training utilized human-in-the-loop quality-assurance labels (yes/no per candidate) on a combined dataset of 30 subjects (11,424 candidates).
  • Nested 3x5-fold cross-validation and data augmentation were employed during model training and evaluation.

Main Results:

  • The cascade pipeline achieved a high AUC of 0.9587, with sensitivity 0.712, specificity 0.975, PPV 0.676, and F1 score 0.693.
  • The system significantly reduced false positives by 76.8% compared to initial candidates while maintaining competitive sensitivity.
  • Inference on 141 scans detected a mean of 40.3 CMBs per scan, with a neurologist preferring the output in 85% of high CMB cases.

Conclusions:

  • The developed automated pipeline offers a robust and efficient method for CMB detection in SWI.
  • This approach effectively mitigates false positives, enhancing diagnostic accuracy for small vessel disease and CAA.
  • The pipeline's output, including NIfTI segmentations and visualizations, is suitable for clinical radiologist review.

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