Antemortem detection of Parkinson's disease pathology in peripheral biopsies using artificial intelligence.

Journal: Acta neuropathologica communications
Published Date:

Abstract

The diagnosis of Parkinson's disease (PD) is challenging at all stages due to variable symptomatology, comorbidities, and mimicking conditions. Postmortem assessment remains the gold standard for a definitive diagnosis. While it is well recognized that PD manifests pathologically in the central nervous system with aggregation of α-synuclein as Lewy bodies and neurites, similar Lewy-type synucleinopathy (LTS) is additionally found in the peripheral nervous system that may be useful as an antemortem biomarker. We have previously found that detection of LTS in submandibular gland (SMG) biopsies is sensitive and specific for advanced PD; however, the sensitivity is suboptimal especially for early-stage disease. Further, visual microscopic assessment of biopsies by a neuropathologist to identify LTS is impractical for large-scale adoption. Here, we trained and validated a convolutional neural network (CNN) for detection of LTS on 283 digital whole slide images (WSI) from 95 unique SMG biopsies. A total of 8,450 LTS and 35,066 background objects were annotated following an inter-rater reliability study with Fleiss Kappa = 0.72. We used transfer learning to train a CNN model to classify image patches (151 × 151 pixels at 20× magnification) with and without the presence of LTS objects. The trained CNN model showed the following performance on image patches: sensitivity: 0.99, specificity: 0.99, precision: 0.81, accuracy: 0.99, and F-1 score: 0.89. We further tested the trained network on 1230 naïve WSI from the same cohort of research subjects comprising 42 PD patients and 14 controls. Logistic regression models trained on features engineered from the CNN predictions on the WSI resulted in sensitivity: 0.71, specificity: 0.65, precision: 0.86, accuracy: 0.69, and F-1 score: 0.76 in predicting clinical PD status, and 0.64 accuracy in predicting PD stage, outperforming expert neuropathologist LTS density scoring in terms of sensitivity but not specificity. These findings demonstrate the practical utility of a CNN detector in screening for LTS, which can translate into a computational tool to facilitate the antemortem tissue-based diagnosis of PD in clinical settings.

Authors

  • Maxim Signaevsky
    Department of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Bahram Marami
    The Center for Computational and Systems Pathology, Department of Pathology, Icahn School of Medicine at Mount Sinai and The Mount Sinai Hospital, New York, USA.
  • Marcel Prastawa
    Department of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Nabil Tabish
    Department of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Megan A Iida
    Department of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Xiang Fu Zhang
    Center for Computational and Systems Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Mary Sawyer
    Center for Computational and Systems Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Israel Duran
    Center for Computational and Systems Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Daniel G Koenigsberg
    Department of Pathology, Icahn School of Medicine at Mount Sinai, 1 Gustave L. Levy Place, Box 1194, New York, NY, 10029, USA.
  • Clare H Bryce
    Department of Pathology, Icahn School of Medicine at Mount Sinai, 1 Gustave L. Levy Place, Box 1194, New York, NY, 10029, USA.
  • Lana M Chahine
    Department of Neurology, University of Pittsburgh, Pittsburgh, PA, USA.
  • Brit Mollenhauer
    Center of Parkinsonism and Movement Disorders Paracelsus, Elena Klinik Kassel and University Medical Center Göttingen, Göttingen, Germany.
  • Sherri Mosovsky
    Department of Neurology, University of Pittsburgh, Pittsburgh, PA, USA.
  • Lindsey Riley
    The Michael J. Fox Foundation for Parkinson's Research, New York, NY, USA.
  • Kuldip D Dave
    The Michael J. Fox Foundation for Parkinson's Research, New York, NY, USA.
  • Jamie Eberling
    The Michael J. Fox Foundation for Parkinson's Research, New York, NY, USA.
  • Chris S Coffey
    University of Iowa, Iowa City, IA, USA.
  • Charles H Adler
    Department of Neurology, Mayo Clinic College of Medicine, Scottsdale, AZ, USA.
  • Geidy E Serrano
    Civin Laboratory for Neuropathology, Banner Sun Health Research Institute, Sun City, AZ, USA.
  • Charles L White
    Neuropathology Laboratory, Department of Pathology, UT Southwestern Medical Center, Dallas, TX, 75390, USA.
  • John Koll
    Department of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Gerardo Fernandez
    Department of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Jack Zeineh
    Department of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Carlos Cordon-Cardo
    Department of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Thomas G Beach
    Civin Laboratory for Neuropathology, Banner Sun Health Research Institute, Sun City, AZ, USA.
  • John F Crary
    Department of Pathology, Nash Family Department of Neuroscience, Department of Artificial Intelligence & Human Health, Neuropathology Brain Bank & Research CoRE, Ronald M. Loeb Center for Alzheimer's Disease, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.