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  1. Home
  2. The Microstructure-weighted Human Connectome: Network Properties And Structure-function Correlations Across Spatial Scales.
  1. Home
  2. The Microstructure-weighted Human Connectome: Network Properties And Structure-function Correlations Across Spatial Scales.

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Modeling the Functional Network for Spatial Navigation in the Human Brain
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The microstructure-weighted human connectome: network properties and structure-function correlations across spatial

Arthur P C Spencer1, Saina Asadi1,2, Yasser Alemán-Gómez1,2

  • 1Department of Radiology, Lausanne University Hospital (CHUV), Lausanne, Switzerland.

Biorxiv : the Preprint Server for Biology
|June 4, 2026

View abstract on PubMed

Summary
This summary is machine-generated.

New brain connectome weights using biophysical diffusion modeling reveal more specific microstructural details. These novel metrics, intra-axonal signal fraction (f) and perpendicular extra-axonal diffusivity (D⊥), better capture structure-function relationships in the brain.

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Co-analysis of Brain Structure and Function using fMRI and Diffusion-weighted Imaging
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Co-analysis of Brain Structure and Function using fMRI and Diffusion-weighted Imaging
17:06

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Published on: November 8, 2012

Area of Science:

  • Neuroimaging
  • Computational Neuroscience
  • Biophysics

Background:

  • Conventional connectome edge weights (e.g., number of streamlines) lack microstructural specificity.
  • Biophysical diffusion modeling offers greater detail about white matter microstructure.

Purpose of the Study:

  • Investigate if biophysical diffusion model parameters can serve as informative connectome weights.
  • Assess the specificity and functional relevance of novel connectome metrics.

Main Methods:

  • Used diffusion MRI data from healthy adults.
  • Constructed structural networks weighted by intra-axonal signal fraction (f), perpendicular extra-axonal diffusivity (D⊥), number of streamlines (NOS), fractional anisotropy (FA), and radial diffusivity (RD).
  • Correlated weighted connectomes with resting-state fMRI and intracranial conduction velocity measurements.

Main Results:

  • All weights showed small-world network properties.
  • Intra-axonal signal fraction (f), perpendicular extra-axonal diffusivity (D⊥), and normalized NOS captured non-random local organization.
  • Only D⊥ demonstrated significant structure-function coupling across all scales and modalities.
  • f and radial diffusivity (RD) showed high consistency in regional structure-function coupling.

Conclusions:

  • Connectome weights derived from biophysical diffusion modeling, particularly D⊥, capture meaningful aspects of brain network organization.
  • These novel metrics offer improved specificity for understanding macroscale brain organization and function.