F.J. Martinez-Murcia
  • Home
  • Research
  • Publications
  • Teaching
  • Communication
  • Blog

Bridging Imaging and Clinical Scores in Parkinson’s Progression Via Multimodal Self-Supervised Deep Learning

LATiDOS
neurodegenerative disease progression
Alzheimer’s Disease
Authors
Affiliations

Francisco J. Martinez-Murcia

Dept. of Signal Theory, Networking and Communications

Andalusian Institute for Data Science and Artificial Intelligence (DASCI)

Juan Eloy Arco

Dept. of Signal Theory, Networking and Communications

Andalusian Institute for Data Science and Artificial Intelligence (DASCI)

Carmen Jimenez-Mesa

Dept. of Signal Theory, Networking and Communications

Andalusian Institute for Data Science and Artificial Intelligence (DASCI)

Fermin Segovia

Dept. of Signal Theory, Networking and Communications

Andalusian Institute for Data Science and Artificial Intelligence (DASCI)

Ignacio A. Illan

Dept. of Signal Theory, Networking and Communications

Andalusian Institute for Data Science and Artificial Intelligence (DASCI)

Javier Ramirez

Dept. of Signal Theory, Networking and Communications

Andalusian Institute for Data Science and Artificial Intelligence (DASCI)

Juan Manuel Gorriz

Dept. of Signal Theory, Networking and Communications

Andalusian Institute for Data Science and Artificial Intelligence (DASCI)

Published

May 22, 2024

Abstract
Neurodegenerative diseases pose a formidable challenge to medical research, demanding a nuanced understanding of their progressive nature. In this regard, latent generative models can effectively be used in a data-driven modeling of different dimensions of neurodegeneration, framed within the context of the manifold hypothesis. This paper proposes a joint framework for a multi-modal, common latent generative model to address the need for a more comprehensive understanding of the neurodegenerative landscape in the context of Parkinson’s disease (PD). The proposed architecture uses coupled variational autoencoders (VAEs) to joint model a common latent space to both neuroimaging and clinical data from the Parkinson’s Progression Markers Initiative (PPMI). Alternative loss functions, different normalization procedures, and the interpretability and explainability of latent generative models are addressed, leading to a model that was able to predict clinical symptomatology in the test set, as measured by the unified Parkinson’s disease rating scale (UPDRS), with R2 up to 0.86 for same-modality and 0.441 cross-modality (using solely neuroimaging). The findings provide a foundation for further advancements in the field of clinical research and practice, with potential applications in decision-making processes for PD. The study also highlights the limitations and capabilities of the proposed model, emphasizing its direct interpretability and potential impact on understanding and interpreting neuroimaging patterns associated with PD symptomatology.

Citation

BibTeX citation:
@article{martinez-murcia2024,
  author = {Martinez-Murcia, Francisco J. and Arco, Juan Eloy and
    Jimenez-Mesa, Carmen and Segovia, Fermin and Illan, Ignacio A. and
    Ramirez, Javier and Gorriz, Juan Manuel},
  title = {Bridging {Imaging} and {Clinical} {Scores} in {Parkinson’s}
    {Progression} {Via} {Multimodal} {Self-Supervised} {Deep}
    {Learning}},
  journal = {International Journal of Neural Systems},
  volume = {34},
  number = {08},
  pages = {2450043},
  date = {2024-05-22},
  url = {https://www.worldscientific.com/doi/abs/10.1142/S0129065724500436},
  doi = {10.1142/S0129065724500436},
  langid = {en},
  abstract = {Neurodegenerative diseases pose a formidable challenge to
    medical research, demanding a nuanced understanding of their
    progressive nature. In this regard, latent generative models can
    effectively be used in a data-driven modeling of different
    dimensions of neurodegeneration, framed within the context of the
    manifold hypothesis. This paper proposes a joint framework for a
    multi-modal, common latent generative model to address the need for
    a more comprehensive understanding of the neurodegenerative
    landscape in the context of Parkinson’s disease (PD). The proposed
    architecture uses coupled variational autoencoders (VAEs) to joint
    model a common latent space to both neuroimaging and clinical data
    from the Parkinson’s Progression Markers Initiative (PPMI).
    Alternative loss functions, different normalization procedures, and
    the interpretability and explainability of latent generative models
    are addressed, leading to a model that was able to predict clinical
    symptomatology in the test set, as measured by the unified
    Parkinson’s disease rating scale (UPDRS), with R2 up to 0.86 for
    same-modality and 0.441 cross-modality (using solely neuroimaging).
    The findings provide a foundation for further advancements in the
    field of clinical research and practice, with potential applications
    in decision-making processes for PD. The study also highlights the
    limitations and capabilities of the proposed model, emphasizing its
    direct interpretability and potential impact on understanding and
    interpreting neuroimaging patterns associated with PD
    symptomatology.}
}
For attribution, please cite this work as:
Martinez-Murcia, Francisco J., Juan Eloy Arco, Carmen Jimenez-Mesa, Fermin Segovia, Ignacio A. Illan, Javier Ramirez, and Juan Manuel Gorriz. 2024. “Bridging Imaging and Clinical Scores in Parkinson’s Progression Via Multimodal Self-Supervised Deep Learning.” International Journal of Neural Systems 34 (08): 2450043. https://doi.org/10.1142/S0129065724500436.