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Neuroimage. 2019 Oct 1;199:289-303. doi: 10.1016/j.neuroimage.2019.05.061. Epub 2019 May 26.

Validating the sensitivity of inhomogeneous magnetization transfer (ihMT) MRI to myelin with fluorescence microscopy.

Author information

1
Aix Marseille Univ, CNRS, CRMBM - UMR 7339, Marseille, France. Electronic address: guillaume.duhamel@univ-amu.fr.
2
Aix Marseille Univ, CNRS, CRMBM - UMR 7339, Marseille, France.
3
Aix Marseille Univ, CNRS, IBDM - UMR 7288, Marseille, France.
4
Department of Radiology, Division of MR Research, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, 02215, USA.

Abstract

Inhomogeneous Magnetization Transfer (ihMT) is a development from the MT MRI technique. IhMT can be considered as a dipolar order relaxation time (T1D) weighted imaging modality whose signal has shown an enhanced selectivity for myelin-rich structures. However, a formal validation of the ihMT sensitivity relative to a gold standard myelin density measurement has not yet been reported. To address this need, we compared ihMT MRI with green fluorescence protein (GFP) microscopy, in a study performed on genetically-modified plp-GFP mice, considered as a reference technique for myelin-content assessment. Various ihMT protocols consisting of variable T1D-filtering and radiofrequency power temporal distributions, were used for comparison with fluorescence microscopy. Strong and significant linear relationships (r2 (0.87-0.96), p < 0.0001) were found between GFP and ihMT ratio signals across brain regions for all tested protocol variants. Conventional MT ratios showed weaker correlations (r2 (0.24-0.78), p ≤ 0.02) and a much larger signal fraction unrelated to myelin, hence corresponding to a much lower specificity for myelin. T1D-filtering reduced the ihMT signal fraction not attributed to myelin by almost twofold relative to zero filtering suggesting that at least half of the unrelated signal has a substantially shorter T1D than myelin. Overall, these results strongly support the sensitivity of ihMT to myelin content.

KEYWORDS:

Fluorescence microscopy; Inhomogeneous magnetization transfer; MRI; Myelin imaging; ihMT; plp-GFP

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