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Reduced cross‐scanner variability using vendor‐agnostic sequences for single‐shell diffusion MRI.

Authors :
Liu, Qiang
Ning, Lipeng
Shaik, Imam Ahmed
Liao, Congyu
Gagoski, Borjan
Bilgic, Berkin
Grissom, William
Nielsen, Jon‐Fredrik
Zaitsev, Maxim
Rathi, Yogesh
Source :
Magnetic Resonance in Medicine; Jul2024, Vol. 92 Issue 1, p246-256, 11p
Publication Year :
2024

Abstract

Purpose: To reduce the inter‐scanner variability of diffusion MRI (dMRI) measures between scanners from different vendors by developing a vendor‐neutral dMRI pulse sequence using the open‐source vendor‐agnostic Pulseq platform. Methods: We implemented a standard EPI based dMRI sequence in Pulseq. We tested it on two clinical scanners from different vendors (Siemens Prisma and GE Premier), systematically evaluating and comparing the within‐ and inter‐scanner variability across the vendors, using both the vendor‐provided and Pulseq dMRI sequences. Assessments covered both a diffusion phantom and three human subjects, using standard error (SE) and Lin's concordance correlation to measure the repeatability and reproducibility of standard DTI metrics including fractional anisotropy (FA) and mean diffusivity (MD). Results: Identical dMRI sequences were executed on both scanners using Pulseq. On the phantom, the Pulseq sequence showed more than a 2.5× reduction in SE (variability) across Siemens and GE scanners. Furthermore, Pulseq sequences exhibited markedly reduced SE in‐vivo, maintaining scan‐rescan repeatability while delivering lower variability in FA and MD (more than 50% reduction in cortical/subcortical regions) compared to vendor‐provided sequences. Conclusion: The Pulseq diffusion sequence reduces the cross‐scanner variability for both phantom and in‐vivo data, which will benefit multi‐center neuroimaging studies and improve the reproducibility of neuroimaging studies. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
07403194
Volume :
92
Issue :
1
Database :
Complementary Index
Journal :
Magnetic Resonance in Medicine
Publication Type :
Academic Journal
Accession number :
176868695
Full Text :
https://doi.org/10.1002/mrm.30062