Accelerating massively parallel hemodynamic models of coarctation of the aorta using neural networks.

Journal: Scientific reports
Published Date:

Abstract

Comorbidities such as anemia or hypertension and physiological factors related to exertion can influence a patient's hemodynamics and increase the severity of many cardiovascular diseases. Observing and quantifying associations between these factors and hemodynamics can be difficult due to the multitude of co-existing conditions and blood flow parameters in real patient data. Machine learning-driven, physics-based simulations provide a means to understand how potentially correlated conditions may affect a particular patient. Here, we use a combination of machine learning and massively parallel computing to predict the effects of physiological factors on hemodynamics in patients with coarctation of the aorta. We first validated blood flow simulations against in vitro measurements in 3D-printed phantoms representing the patient's vasculature. We then investigated the effects of varying the degree of stenosis, blood flow rate, and viscosity on two diagnostic metrics - pressure gradient across the stenosis (ΔP) and wall shear stress (WSS) - by performing the largest simulation study to date of coarctation of the aorta (over 70 million compute hours). Using machine learning models trained on data from the simulations and validated on two independent datasets, we developed a framework to identify the minimal training set required to build a predictive model on a per-patient basis. We then used this model to accurately predict ΔP (mean absolute error within 1.18 mmHg) and WSS (mean absolute error within 0.99 Pa) for patients with this disease.

Authors

  • Bradley Feiger
    Department of Biomedical Engineering, Duke University, Durham, NC, USA.
  • John Gounley
    Advanced Computing for Health Sciences, Oak Ridge National Laboratory, Oak Ridge, TN 37830, United States.
  • Dale Adler
    Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Jane A Leopold
    Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Erik W Draeger
    Lawrence Livermore National Laboratory, Livermore, CA, USA.
  • Rafeed Chaudhury
    Department of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, USA.
  • Justin Ryan
    Department of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, USA.
  • Girish Pathangey
    Department of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, USA.
  • Kevin Winarta
    Department of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, USA.
  • David Frakes
    Department of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, USA.
  • Franziska Michor
    Department of Department of Data Sciences, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Amanda Randles
    Department of Biomedical Engineering, Duke University, Durham, NC, USA. amanda.randles@duke.edu.