AI Article Synopsis

  • A multiparameter mapping (MPM) protocol was established for high reproducibility in multicenter MRI studies using standardized sequences from various vendors, ensuring consistency across different sites and scanner types.
  • The study utilized six 3T MRI scanners and measured four key metrics (MT, PD, R1, and R2*) in a 20-minute scan session involving five participants across multiple sessions, showing low variability (CoV 4-10%) for most measurements.
  • The MPM protocol yielded precise and reliable quantitative maps suitable for tracking microstructural changes in clinical trials, demonstrating its potential as a valuable MRI biomarker.

Article Abstract

Multicenter clinical and quantitative magnetic resonance imaging (qMRI) studies require a high degree of reproducibility across different sites and scanner manufacturers, as well as time points. We therefore implemented a multiparameter mapping (MPM) protocol based on vendor's product sequences and demonstrate its repeatability and reproducibility for whole-brain coverage. Within ~20 min, four MPM metrics (magnetization transfer saturation [MT], proton density [PD], longitudinal [R1], and effective transverse [R2*] relaxation rates) were measured using an optimized 1 mm isotropic resolution protocol on six 3 T MRI scanners from two different vendors. The same five healthy participants underwent two scanning sessions, on the same scanner, at each site. MPM metrics were calculated using the hMRI-toolbox. To account for different MT pulses used by each vendor, we linearly scaled the MT values to harmonize them across vendors. To determine longitudinal repeatability and inter-site comparability, the intra-site (i.e., scan-rescan experiment) coefficient of variation (CoV), inter-site CoV, and bias across sites were estimated. For MT, R1, and PD, the intra- and inter-site CoV was between 4 and 10% across sites and scan time points for intracranial gray and white matter. A higher intra-site CoV (16%) was observed in R2* maps. The inter-site bias was below 5% for all parameters. In conclusion, the MPM protocol yielded reliable quantitative maps at high resolution with a short acquisition time. The high reproducibility of MPM metrics across sites and scan time points combined with its tissue microstructure sensitivity facilitates longitudinal multicenter imaging studies targeting microstructural changes, for example, as a quantitative MRI biomarker for interventional clinical trials.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7502832PMC
http://dx.doi.org/10.1002/hbm.25122DOI Listing

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