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.

Highlights

  • Multicenter clinical studies using magnetic resonance imaging (MRI) increase the size and diversity of the study population (Van Horn & Toga, 2009)

  • In this article we report the scan-rescan repeatability and inter-site comparability of the multiparameter mapping (MPM) protocol across six different clinical sites involved in the NISCI trial

  • This study investigated scan-rescan and inter-site reproducibility of the multiparameter mapping (MPM) approach implemented, at 3 T MRI, with Philips and Siemens vendor sequences

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Summary

Introduction

Multicenter clinical studies using magnetic resonance imaging (MRI) increase the size and diversity of the study population (Van Horn & Toga, 2009). The multiparameter mapping (MPM) method (Helms, Dathe, Kallenberg, & Dechent, 2008; Weiskopf et al, 2013) provides quantitative high-resolution maps (magnetization transfer saturation [MT], proton density [PD], longitudinal and effective transverse relaxation [R1, R2*]) sensitive to myelin and iron content in the brain within clinically feasible scan times (20 min). MPM has been applied in a wide range of studies to investigate microstructural tissue properties in gray and white matter and has proven its potential to provide quantitative imaging biomarkers (Callaghan et al, 2014; Freund et al, 2013; Grabher et al, 2015; Seif et al, 2018; Weiskopf et al, 2013; Ziegler et al, 2018)

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