Volume 94, Issue 3 pp. 1103-1118
RESEARCH ARTICLE

Quantitative muscle water T2 mapping using RF phase-modulated 3D gradient echo imaging

Eléonore Vermeulen

Corresponding Author

Eléonore Vermeulen

NMR Laboratory, Neuromuscular Investigation Center, Institute of Myology, Paris, France

Correspondence

Eléonore Vermeulen, Institute of Myology, Bâtiment Babinski, Groupe Hospitalier Pitié-Salpêtrière, 47-83 boulevard Vincent Auriol, 75651 Paris Cedex 13, Paris, France.

Email: [email protected]

Search for more papers by this author
Pierre-Yves Baudin

Pierre-Yves Baudin

NMR Laboratory, Neuromuscular Investigation Center, Institute of Myology, Paris, France

Search for more papers by this author
Marc Lapert

Marc Lapert

Siemens Healthcare SAS, Courbevoie, France

Search for more papers by this author
Benjamin Marty

Benjamin Marty

NMR Laboratory, Neuromuscular Investigation Center, Institute of Myology, Paris, France

Search for more papers by this author
First published: 06 May 2025

Abstract

Purpose

To propose a motion robust 3D sequence for water T2 ( T 2 H 2 O $$ \mathrm{T}{2}_{{\mathrm{H}}_2\mathrm{O}} $$ ) estimation in skeletal muscle tissues.

Methods

A T 2 H 2 O $$ \mathrm{T}{2}_{{\mathrm{H}}_2\mathrm{O}} $$ estimation method is proposed, using 10 image volumes acquired with a partially spoiled gradient echo (pSPGR) sequence, varying the RF phase-cycling increment and prescribed flip angle. The complex signal evolution is fit with a bi-component water/fat model to extract T 2 H 2 O $$ \mathrm{T}{2}_{{\mathrm{H}}_2\mathrm{O}} $$ and account for B1 and fat fraction confounders. Accuracy and precision were evaluated using numerical simulations. Cartesian and radial implementations of the sequence were tested. In phantoms, results were compared with reference spectroscopic and multi-spin echo imaging techniques. Several in vivo experiments evaluated robustness to B1 field inhomogeneities, sensitivity to physiological and pathological variations in T 2 H 2 O $$ \mathrm{T}{2}_{{\mathrm{H}}_2\mathrm{O}} $$ on the thigh muscles.

Results

In phantoms, T 2 H 2 O $$ \mathrm{T}{2}_{{\mathrm{H}}_2\mathrm{O}} $$ values were highly correlated with reference spectroscopy and multi spin echo values (R2 > 0.8). In vivo, T 2 H 2 O $$ \mathrm{T}{2}_{{\mathrm{H}}_2\mathrm{O}} $$ values were correlated with reference values in healthy controls (R2 = 0.69) and pathological muscles (R2 = 0.87) and were not affected by B1 inhomogeneities (R2 = 0.06). In the tongue muscle, a significant reduction in the SD of T 2 H 2 O $$ \mathrm{T}{2}_{{\mathrm{H}}_2\mathrm{O}} $$ values was observed using the radial compared to the Cartesian pSPGR sequence (−28%).

Conclusion

The proposed approach provides efficient 3D T 2 H 2 O $$ \mathrm{T}{2}_{{\mathrm{H}}_2\mathrm{O}} $$ estimation in skeletal muscle, including small moving organs like the tongue. This broadens the range of accessible targets for characterizing heterogeneous impairment of muscle tissue, while retaining durations compatible with clinical research.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.