# Verifying the concordance between motion corrected and conventional MPRAGE for pediatric morphometric analysis

**Authors:** Barat Gal-Er, Yannick Brackenier, Alexandra F. Bonthrone, Chiara Casella, Anthony Price, Sophie Arulkumaran, Andrew T. M. Chew, Chiara Nosarti, Michela Cleri, Pierluigi Di Cio, Alexia Egloff, Mary A. Rutherford, Jonathan O’Muircheartaigh, Raphael Tomi-Tricot, Shaihan Malik, Lucilio Cordero-Grande, Joseph V. Hajnal, Serena J. Counsell

PMC · DOI: 10.3389/fnins.2025.1534924 · Frontiers in Neuroscience · 2025-05-09

## TL;DR

This study shows that a new motion correction technique called DISORDER produces reliable brain measurements in children, even when motion is present, improving on conventional methods.

## Contribution

The study validates DISORDER as a motion correction technique for pediatric brain morphometry, showing improved reliability over conventional MPRAGE in motion-corrupted scans.

## Key findings

- DISORDER showed good/excellent agreement with conventional MPRAGE for most subcortical GM and regional brain volumes.
- Motion-corrupt conventional MPRAGE had significantly greater differences compared to DISORDER data in 22/58 brain structures.
- DISORDER provides more reliable morphometric measures in motion-degraded pediatric scans than conventional MPRAGE.

## Abstract

This study aimed to validate a retrospective motion correction technique, Distributed and Incoherent Sample Orders for Reconstruction Deblurring using Encoding Redundancy (DISORDER), for pediatric brain morphometry.

Two T1-weighted MPRAGE 3D datasets were acquired at 3 T in thirty-seven children aged 7–8 years: one with conventional linear phase encoding and one using DISORDER. MPRAGE images were scored as motion-free or motion-corrupt. Cortical morphometry and regional brain volumes were measured with FreeSurfer, subcortical grey matter (GM) with FSL-FIRST, and hippocampi with HippUnfold. Intraclass correlation coefficient (ICC) was used to determine agreement. Mann–Whitney U was used to test the difference between measures obtained using DISORDER and (i) motion-free and (ii) motion-corrupt conventional MPRAGE data.

ICC measures between conventional MPRAGE and DISORDER data were good/excellent for most subcortical GM (motion-free, 0.75–0.96; motion-corrupt, 0.62–0.98) and regional brain volumes (motion-free 0.47–0.99; motion-corrupt, 0.54–0.99), except for the amygdala and nucleus accumbens (motion-free, 0.38–0.65; motion-corrupt, 0.1–0.42). These values were less consistent for motion-corrupt conventional MPRAGE data for hippocampal volumes (motion-free 0.65–0.99; motion-corrupt, 0.11–0.91) and cortical measures (motion-free 0.76–0.98; motion-corrupt, 0.09–0.74). Mann–Whitney U showed percentage differences in measures obtained with motion-corrupt conventional MPRAGE compared to DISORDER data were significantly greater than in those obtained using motion-free conventional MPRAGE data in 22/58 structures.

In the absence of motion, morphometric measures obtained using DISORDER are largely consistent with those from conventional MPRAGE data, whereas improved reliability is obtained by DISORDER for motion-degraded scans. This study validates the use of DISORDER for brain morphometric studies in children.

## Full-text entities

- **Genes:** CA3 (carbonic anhydrase 3) [NCBI Gene 761] {aka CAIII, Car3}, CA2 (carbonic anhydrase 2) [NCBI Gene 760] {aka CA-II, CAC, CAII, Car2, HEL-76, HEL-S-282}, CA1 (carbonic anhydrase 1) [NCBI Gene 759] {aka CA-I, CAB, Car1, HEL-S-11}, CA4 (carbonic anhydrase 4) [NCBI Gene 762] {aka CAIV, Car4, RP17}
- **Diseases:** epilepsy (MESH:D004827), ADHD (MESH:D001289), CHD (MESH:D006330), brain asymmetry (MESH:D005146), motion (MESH:D009041), DISORDER (MESH:D009358)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12098291/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12098291/full.md

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Source: https://tomesphere.com/paper/PMC12098291