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Tau follows principal axes of functional and structural brain organization in Alzheimer’s disease

Author

Listed:
  • Julie Ottoy

    (University of Toronto)

  • Min Su Kang

    (University of Toronto)

  • Jazlynn Xiu Min Tan

    (University of Toronto)

  • Lyndon Boone

    (University of Toronto)

  • Reinder Vos de Wael

    (McGill University)

  • Bo-yong Park

    (Inha University
    Institute for Basic Science)

  • Gleb Bezgin

    (McGill University
    McGill University)

  • Firoza Z. Lussier

    (McGill University
    University of Pittsburgh)

  • Tharick A. Pascoal

    (University of Pittsburgh)

  • Nesrine Rahmouni

    (McGill University)

  • Jenna Stevenson

    (McGill University)

  • Jaime Fernandez Arias

    (McGill University)

  • Joseph Therriault

    (McGill University)

  • Seok-Jun Hong

    (Sungkyunkwan University)

  • Bojana Stefanovic

    (University of Toronto
    University of Toronto
    University of Toronto)

  • JoAnne McLaurin

    (University of Toronto
    University of Toronto
    University of Toronto)

  • Jean-Paul Soucy

    (McGill University)

  • Serge Gauthier

    (McGill University)

  • Boris C. Bernhardt

    (McGill University)

  • Sandra E. Black

    (University of Toronto
    University of Toronto)

  • Pedro Rosa-Neto

    (McGill University
    McGill University)

  • Maged Goubran

    (University of Toronto
    University of Toronto
    University of Toronto)

Abstract

Alzheimer’s disease (AD) is a brain network disorder where pathological proteins accumulate through networks and drive cognitive decline. Yet, the role of network connectivity in facilitating this accumulation remains unclear. Using in-vivo multimodal imaging, we show that the distribution of tau and reactive microglia in humans follows spatial patterns of connectivity variation, the so-called gradients of brain organization. Notably, less distinct connectivity patterns (“gradient contraction”) are associated with cognitive decline in regions with greater tau, suggesting an interaction between reduced network differentiation and tau on cognition. Furthermore, by modeling tau in subject-specific gradient space, we demonstrate that tau accumulation in the frontoparietal and temporo-occipital cortices is associated with greater baseline tau within their functionally and structurally connected hubs, respectively. Our work unveils a role for both functional and structural brain organization in pathology accumulation in AD, and supports subject-specific gradient space as a promising tool to map disease progression.

Suggested Citation

  • Julie Ottoy & Min Su Kang & Jazlynn Xiu Min Tan & Lyndon Boone & Reinder Vos de Wael & Bo-yong Park & Gleb Bezgin & Firoza Z. Lussier & Tharick A. Pascoal & Nesrine Rahmouni & Jenna Stevenson & Jaime , 2024. "Tau follows principal axes of functional and structural brain organization in Alzheimer’s disease," Nature Communications, Nature, vol. 15(1), pages 1-18, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-49300-2
    DOI: 10.1038/s41467-024-49300-2
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    References listed on IDEAS

    as
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