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A deep learning framework identifies dimensional representations of Alzheimer’s Disease from brain structure

Author

Listed:
  • Zhijian Yang

    (University of Pennsylvania
    University of Pennsylvania)

  • Ilya M. Nasrallah

    (University of Pennsylvania
    University of Pennsylvania)

  • Haochang Shou

    (University of Pennsylvania
    University of Pennsylvania)

  • Junhao Wen

    (University of Pennsylvania
    University of Pennsylvania)

  • Jimit Doshi

    (University of Pennsylvania
    University of Pennsylvania)

  • Mohamad Habes

    (University of Pennsylvania
    University of Texas Health Science Center San Antonio (UTHSCSA))

  • Guray Erus

    (University of Pennsylvania
    University of Pennsylvania)

  • Ahmed Abdulkadir

    (University of Pennsylvania
    University of Pennsylvania)

  • Susan M. Resnick

    (National Institute on Aging)

  • Marilyn S. Albert

    (Johns Hopkins University School of Medicine)

  • Paul Maruff

    (University of Melbourne)

  • Jurgen Fripp

    (Australian e-Health Research Centre CSIRO)

  • John C. Morris

    (Washington University in St. Louis)

  • David A. Wolk

    (University of Pennsylvania
    University of Pennsylvania
    University of Pennsylvania)

  • Christos Davatzikos

    (University of Pennsylvania
    University of Pennsylvania)

Abstract

Heterogeneity of brain diseases is a challenge for precision diagnosis/prognosis. We describe and validate Smile-GAN (SeMI-supervised cLustEring-Generative Adversarial Network), a semi-supervised deep-clustering method, which examines neuroanatomical heterogeneity contrasted against normal brain structure, to identify disease subtypes through neuroimaging signatures. When applied to regional volumes derived from T1-weighted MRI (two studies; 2,832 participants; 8,146 scans) including cognitively normal individuals and those with cognitive impairment and dementia, Smile-GAN identified four patterns or axes of neurodegeneration. Applying this framework to longitudinal data revealed two distinct progression pathways. Measures of expression of these patterns predicted the pathway and rate of future neurodegeneration. Pattern expression offered complementary performance to amyloid/tau in predicting clinical progression. These deep-learning derived biomarkers offer potential for precision diagnostics and targeted clinical trial recruitment.

Suggested Citation

  • Zhijian Yang & Ilya M. Nasrallah & Haochang Shou & Junhao Wen & Jimit Doshi & Mohamad Habes & Guray Erus & Ahmed Abdulkadir & Susan M. Resnick & Marilyn S. Albert & Paul Maruff & Jurgen Fripp & John C, 2021. "A deep learning framework identifies dimensional representations of Alzheimer’s Disease from brain structure," Nature Communications, Nature, vol. 12(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-26703-z
    DOI: 10.1038/s41467-021-26703-z
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    References listed on IDEAS

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    1. Alexandra L Young & Razvan V Marinescu & Neil P Oxtoby & Martina Bocchetta & Keir Yong & Nicholas C Firth & David M Cash & David L Thomas & Katrina M Dick & Jorge Cardoso & John Swieten & Barbara Borr, 2018. "Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference," Nature Communications, Nature, vol. 9(1), pages 1-16, December.
    2. Lawrence Hubert & Phipps Arabie, 1985. "Comparing partitions," Journal of Classification, Springer;The Classification Society, vol. 2(1), pages 193-218, December.
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    Cited by:

    1. Zhijian Yang & Junhao Wen & Ahmed Abdulkadir & Yuhan Cui & Guray Erus & Elizabeth Mamourian & Randa Melhem & Dhivya Srinivasan & Sindhuja T. Govindarajan & Jiong Chen & Mohamad Habes & Colin L. Master, 2024. "Gene-SGAN: discovering disease subtypes with imaging and genetic signatures via multi-view weakly-supervised deep clustering," Nature Communications, Nature, vol. 15(1), pages 1-16, December.

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