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Biophysics-based statistical learning: Application to heart and brain interactions.

Jaume Banus1, Marco Lorenzi1, Oscar Camara2

  • 1UniversitĂ© CĂ´te d'Azur, INRIA Sophia Antipolis, Epione Project-Team, France.

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|May 21, 2021
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Summary
This summary is machine-generated.

This study links heart and brain health using UK Biobank data. Personalized cardiovascular models, constrained by brain imaging and clinical data, reveal underlying physiological mechanisms and differences in conditions like atrial fibrillation.

Keywords:
Atrial fibrillationCardiovascular modellingHeart-Brain interactionLumped modelPersonalisationWhite matter damage

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Area of Science:

  • Cardiovascular Imaging and Physiology
  • Neuroimaging and Computational Biology
  • Biophysical Modeling

Background:

  • Large-scale initiatives like UK Biobank offer joint cardiac and brain imaging data.
  • Current research often uses association models, lacking mechanistic insights and prior physiological knowledge.
  • Estimating unobservable cardiovascular parameters (e.g., cardiac contractility) via biophysical models is challenging due to data limitations and ill-posed personalization.

Purpose of the Study:

  • To develop an approach for jointly studying heart and brain by personalizing cardiovascular models.
  • To constrain cardiovascular model parameter personalization using statistical relationships with brain imaging data and clinical information.
  • To explore the physiological plausibility and clinical relevance of these personalized models.

Main Methods:

  • Proposed a constrained parameter personalization approach for a lumped cardiovascular model.
  • Utilized statistical relationships between model parameters and brain-volumetric indices (ventricles, white matter hyperintensities) and clinical data (age, body surface area).
  • Validated the approach by inferring model parameters with and without specific clinical features in a large cohort (>3000 subjects) and a subgroup with atrial fibrillation (59 subjects).

Main Results:

  • Demonstrated that external features significantly improve cardiovascular model personalization by providing informative parameter-space constraints.
  • Learned physiologically plausible mechanisms through personalized cardiovascular models.
  • Identified significant differences associated with specific clinical conditions, such as atrial fibrillation.

Conclusions:

  • Constraining cardiovascular models with brain imaging and clinical data enhances personalization and reveals underlying physiological mechanisms.
  • This integrated approach offers deeper insights into the heart-brain relationship.
  • The method is applicable to large cohorts and can identify condition-specific cardiovascular differences.