4.7 Article

Characterisation of white matter asymmetries in the healthy human brain using diffusion MRI fixel-based analysis

Journal

NEUROIMAGE
Volume 225, Issue -, Pages -

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2020.117505

Keywords

White matter; Asymmetry; Diffusion MRI; Fixel-based analysis

Funding

  1. National Health and Medical Research Council of Australia [APP1091593, APP1117724]
  2. Australian Research Council [DP170101815]
  3. Victorian Government's Operational Infrastructure Support Program
  4. Melbourne Bioinformatics at the University of Melbourne [UOM0048]
  5. National Imaging Facility (NIF), an Australian Government National Collaborative Research Infrastructure Strategy (NCRIS) capability
  6. NIH Blueprint for Neuroscience Research [1U54MH091657]
  7. McDonnell centre for Systems Neuroscience at Washington University [1U54MH091657]

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The study provides a more robust characterization of human brain white matter asymmetries using fiber-specific diffusion MRI metrics and a whole-brain data-driven approach. Significant asymmetries were found throughout the brain white matter, with no influences of sex, age, or handedness observed on the asymmetry.
The diffusion tensor model for diffusion MRI has been used extensively to study asymmetry in the human brain white matter. However, given the limitations of the tensor model, the nature of any underlying asymmetries remains uncertain, particularly in crossing fibre regions. Here, we provide a more robust characterisation of human brain white matter asymmetries based on fibre-specific diffusion MRI metrics and a whole-brain datadriven approach. We used high-quality diffusion MRI data (n = 100) from the Human Connectome Project, the spherical deconvolution model for fibre orientation distribution estimation, and the Fixel-Based Analysis framework to utilise crossing fibre information in registration, data smoothing and statistical inference. We found many significant asymmetries, widespread throughout the brain white matter, with both left >right and right >left dominances observed in different pathways. No influences of sex, age, or handedness on asymmetry were found. We also report on the relative contributions of microstructural and morphological white matter properties toward the asymmetry findings. Our findings should provide important information to future studies focussing on how these asymmetries are affected by disease, development/ageing, or how they correlate to functional/cognitive measures.

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