Mesoscale Whole-Brain T2*-Weighted and Associated Quantitative MRI in Humans at 10.5 T

Magn Reson Med. 2026 Aug;96(2):817-825. doi: 10.1002/mrm.70366. Epub 2026 Apr 7.

Abstract

Purpose: To demonstrate mesoscale whole-brain T2*-weighted (T2*w) MRI at 10.5 T, quantify R2* relaxation rate and magnetic susceptibility (χ), and evaluate T2*w contrast at such high field strength.

Methods: Multi-echo GRE (ME-GRE) data were collected in healthy adults at 0.5 mm isotropic resolution at 10.5 T. Whole-brain images were reconstructed with navigator-guided joint motion and field correction and were used for quantitative R2* and χ mapping. Regional R2* and χ values and R2* contrast were analyzed in volumetric regions of interest (ROIs) and intra-cortical surface-based ROIs. For comparison, ME-GRE data from the same subjects were acquired using a similar protocol at 7 T.

Results: High-quality whole-brain T2*w images were obtained, enabling R2* and χ mapping with delineation of fine-scale brain structures. Regional R2* analysis revealed a linear relationship between 10.5 T and 7 T R2* values with a slope of 1.52, in agreement with previously reported linear field dependency of R2*. Estimated χ values were field-independent in most brain regions under consideration except for the basal ganglia where χ was observed to be lower at 10.5 T than at 7 T. The normalized R2* contrast that is, the R2* difference normalized by the mean R2*, increased by about 3% between brain regions and 12% between cortical depths from 7 to 10.5 T.

Conclusion: It is feasible to achieve high-quality mesoscale whole-brain T2*w MRI at 10.5 T and associated quantitative R2* and χ mapping. Our results may aid future optimization of anatomic T2*w brain MRI at ultrahigh field beyond 7 T.

Keywords: 10.5 T; R2* relaxation rate; T2*‐weighted MRI; magnetic susceptibility χ; mesoscale whole‐brain MRI; ultrahigh field MRI.

MeSH terms

  • Adult
  • Algorithms
  • Brain Mapping / methods
  • Brain* / diagnostic imaging
  • Female
  • Humans
  • Image Processing, Computer-Assisted* / methods
  • Magnetic Resonance Imaging* / methods
  • Male