Frontiers in Neuroscience (Aug 2023)

Fiber-orientation independent component of R2* obtained from single-orientation MRI measurements in simulations and a post-mortem human optic chiasm

  • Francisco J. Fritz,
  • Laurin Mordhorst,
  • Mohammad Ashtarayeh,
  • Joao Periquito,
  • Andreas Pohlmann,
  • Markus Morawski,
  • Markus Morawski,
  • Carsten Jaeger,
  • Carsten Jaeger,
  • Thoralf Niendorf,
  • Kerrin J. Pine,
  • Martina F. Callaghan,
  • Nikolaus Weiskopf,
  • Nikolaus Weiskopf,
  • Siawoosh Mohammadi,
  • Siawoosh Mohammadi,
  • Siawoosh Mohammadi

DOI
https://doi.org/10.3389/fnins.2023.1133086
Journal volume & issue
Vol. 17

Abstract

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The effective transverse relaxation rate (R2*) is sensitive to the microstructure of the human brain like the g-ratio which characterises the relative myelination of axons. However, the fibre-orientation dependence of R2* degrades its reproducibility and any microstructural derivative measure. To estimate its orientation-independent part (R2,iso*) from single multi-echo gradient-recalled-echo (meGRE) measurements at arbitrary orientations, a second-order polynomial in time model (hereafter M2) can be used. Its linear time-dependent parameter, β1, can be biophysically related to R2,iso* when neglecting the myelin water (MW) signal in the hollow cylinder fibre model (HCFM). Here, we examined the performance of M2 using experimental and simulated data with variable g-ratio and fibre dispersion. We found that the fitted β1 can estimate R2,iso* using meGRE with long maximum-echo time (TEmax ≈ 54 ms), but not accurately captures its microscopic dependence on the g-ratio (error 84%). We proposed a new heuristic expression for β1 that reduced the error to 12% for ex vivo compartmental R2 values. Using the new expression, we could estimate an MW fraction of 0.14 for fibres with negligible dispersion in a fixed human optic chiasm for the ex vivo compartmental R2 values but not for the in vivo values. M2 and the HCFM-based simulations failed to explain the measured R2*-orientation-dependence around the magic angle for a typical in vivo meGRE protocol (with TEmax ≈ 18 ms). In conclusion, further validation and the development of movement-robust in vivo meGRE protocols with TEmax ≈ 54 ms are required before M2 can be used to estimate R2,iso* in subjects.

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