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regionalpcs improve discovery of DNA methylation associations with complex traits

Author

Listed:
  • Tiffany Eulalio

    (Stanford University)

  • Min Woo Sun

    (Stanford University)

  • Olivier Gevaert

    (Stanford University
    Stanford University)

  • Michael D. Greicius

    (Stanford University)

  • Thomas J. Montine

    (Stanford University)

  • Daniel Nachun

    (Stanford University)

  • Stephen B. Montgomery

    (Stanford University
    Stanford University)

Abstract

We have developed the regionalpcs method, an approach for summarizing gene-level methylation. regionalpcs addresses the challenge of deciphering complex epigenetic mechanisms in diseases like Alzheimer’s disease. In contrast to averaging, regionalpcs uses principal components analysis to capture complex methylation patterns across gene regions. Our method demonstrates a 54% improvement in sensitivity over averaging in simulations, providing a robust framework for identifying subtle epigenetic variations. Applying regionalpcs to Alzheimer’s disease brain methylation data, combined with cell type deconvolution, we uncover 838 differentially methylated genes associated with neuritic plaque burden—significantly outperforming conventional methods. Integrating methylation quantitative trait loci with genome-wide association studies identified 17 genes with potential causal roles in Alzheimer’s disease risk, including MS4A4A and PICALM. Available in the Bioconductor package regionalpcs, our approach facilitates a deeper understanding of the epigenetic landscape in Alzheimer’s disease and opens avenues for research into complex diseases.

Suggested Citation

  • Tiffany Eulalio & Min Woo Sun & Olivier Gevaert & Michael D. Greicius & Thomas J. Montine & Daniel Nachun & Stephen B. Montgomery, 2025. "regionalpcs improve discovery of DNA methylation associations with complex traits," Nature Communications, Nature, vol. 16(1), pages 1-19, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-024-55698-6
    DOI: 10.1038/s41467-024-55698-6
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    References listed on IDEAS

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