IDEAS home Printed from https://ideas.repec.org/a/plo/pone00/0342549.html

Disease progression modeling of Alzheimer’s disease based on variational probability principal component analysis

Author

Listed:
  • Xin Xiong
  • Ximin Wang
  • Chenyang Zhu
  • Jianfeng He
  • for the Alzheimer’s Disease Neuroimaging Initiative

Abstract

Alzheimer’s disease (AD) is a neurodegenerative disorder and the leading cause of dementia. Early diagnosis and monitoring of disease progression are crucial for effective intervention. This study presents a novel disease progression model based on Variational Probabilistic Principal Component Analysis (VPPCA), which uses a Bayesian framework for dimensionality reduction and uncertainty quantification. By analyzing 1,021 amyloid-positive patients from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database, we extracted 25 features, including CSF (ABETA, TAU, PTAU), PET (FDG, AV45), and MRI volumetrics, along with cognitive and functional assessments. VPPCA compresses these multi-modal biomarkers into a single first principal component score (VPPCA1), which serves as a measure of disease progression. To ensure biological grounding and avoid circularity, we demonstrated that a VPPCA1 model using only non-cognitive features (CSF, PET, MRI, demographics) correlates strongly with cognitive decline (r = 0.658 with ADAS-Cog13), confirming that it captures genuine pathological progression rather than simply reflecting cognitive assessments. Block-wise feature ablation revealed that multi-modal integration is essential, with cognitive features showing the highest importance (0.1064), though all modalities contribute complementarily. In classification tasks, VPPCA exhibited strong performance with ROC-AUC values of 0.990 (CN vs Dementia), 0.774 (CN vs MCI), and 0.785 (MCI vs Dementia). A Bayesian hierarchical longitudinal model effectively captured patient-specific progression trajectories, offering personalized predictions of future disease states. VPPCA outperforms Probabilistic PCA (PPCA) by providing uncertainty quantification, with patient-specific confidence levels (σ = 0.086–0.136), which correlate with data quality, enabling automatic risk stratification. This work demonstrates that VPPCA offers a robust, biologically-grounded framework for modeling AD progression, providing actionable uncertainty quantification that improves clinical decision support and facilitates personalized care.

Suggested Citation

  • Xin Xiong & Ximin Wang & Chenyang Zhu & Jianfeng He & for the Alzheimer’s Disease Neuroimaging Initiative, 2026. "Disease progression modeling of Alzheimer’s disease based on variational probability principal component analysis," PLOS ONE, Public Library of Science, vol. 21(3), pages 1-26, March.
  • Handle: RePEc:plo:pone00:0342549
    DOI: 10.1371/journal.pone.0342549
    as

    Download full text from publisher

    File URL: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0342549
    Download Restriction: no

    File URL: https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0342549&type=printable
    Download Restriction: no

    File URL: https://libkey.io/10.1371/journal.pone.0342549?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:plo:pone00:0342549. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: plosone (email available below). General contact details of provider: https://journals.plos.org/plosone/ .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.