A framework for combining a motion atlas with non-motion information to learn clinically useful biomarkers: Application to cardiac resynchronisation therapy response prediction.

Journal: Medical image analysis
Published Date:

Abstract

We present a framework for combining a cardiac motion atlas with non-motion data. The atlas represents cardiac cycle motion across a number of subjects in a common space based on rich motion descriptors capturing 3D displacement, velocity, strain and strain rate. The non-motion data are derived from a variety of sources such as imaging, electrocardiogram (ECG) and clinical reports. Once in the atlas space, we apply a novel supervised learning approach based on random projections and ensemble learning to learn the relationship between the atlas data and some desired clinical output. We apply our framework to the problem of predicting response to Cardiac Resynchronisation Therapy (CRT). Using a cohort of 34 patients selected for CRT using conventional criteria, results show that the combination of motion and non-motion data enables CRT response to be predicted with 91.2% accuracy (100% sensitivity and 62.5% specificity), which compares favourably with the current state-of-the-art in CRT response prediction.

Authors

  • Devis Peressutti
    Division of Imaging Sciences and Biomedical Engineering, King's College London, London, United Kingdom. Electronic address: devis.1.peressutti@kcl.ac.uk.
  • Matthew Sinclair
    Division of Imaging Sciences and Biomedical Engineering, King's College London, London, United Kingdom.
  • Wenjia Bai
    Department of Computing Imperial College London London UK.
  • Thomas Jackson
  • Jacobus Ruijsink
    Division of Imaging Sciences and Biomedical Engineering, King's College London, London, United Kingdom.
  • David Nordsletten
    Division of Imaging Sciences and Biomedical Engineering, King's College London, London, United Kingdom.
  • Liya Asner
    Division of Imaging Sciences and Biomedical Engineering, King's College London, London, United Kingdom.
  • Myrianthi Hadjicharalambous
    Division of Imaging Sciences and Biomedical Engineering, King's College London, London, United Kingdom.
  • Christopher A Rinaldi
    Division of Imaging Sciences and Biomedical Engineering, King's College London, London, United Kingdom.
  • Daniel Rueckert
    Biomedical Image Analysis (BioMedIA) Group, Department of Computing, Imperial College London, UK. Electronic address: d.rueckert@imperial.ac.uk.
  • Andrew P King
    Division of Imaging Sciences and Biomedical Engineering, King's College London, London, United Kingdom. Electronic address: andrew.king@kcl.ac.uk.