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Updated: Jun 11, 2026

Quantitative Magnetic Resonance Imaging of Skeletal Muscle Disease
Published on: December 18, 2016
Simultaneous quantification of T2 and T'2 using a combined gradient echo-spin echo sequence at ultrahigh field.
Eleanor F Cox1, Penny A Gowland
1Sir Peter Mansfield Magnetic Resonance Centre, School of Physics and Astronomy, University of Nottingham, United Kingdom. eleanor.cox@nottingham.ac.uk
Gradient echo sampling of spin echo (GESSE) accurately measures T(2) relaxation times at 7.0 Tesla, overcoming radiofrequency inhomogeneity. This method optimizes fitting and timing parameters for precise T(2) and T’(2) estimations in brain tissues.
Area of Science:
- Magnetic Resonance Imaging
- Biophysics
- Neuroimaging
Background:
- Measuring T(2) relaxation times at high magnetic fields (7.0 T) is challenging due to radiofrequency (RF) inhomogeneity.
- Existing methods can be susceptible to RF pulse errors and image distortions.
Purpose of the Study:
- To evaluate gradient echo sampling of a spin echo (GESSE) for T(2) and T'(2) measurements at 7.0 T.
- To optimize GESSE acquisition and analysis parameters for improved accuracy and reduced noise sensitivity.
Main Methods:
- GESSE technique was employed to acquire data at 1.5, 3.0, and 7.0 T.
- Weighted linear fitting and optimized spin echo and gradient echo timing were utilized.
- T(2), T'(2), and T*(2) values were calculated for frontal gray matter, occipital gray matter, and white matter.
Main Results:
- GESSE is insensitive to RF pulse errors and image distortions, enabling simultaneous T(2) and T'(2) estimation.
- A weighted linear fit improved T(2) accuracy compared to nonlinear fitting.
- T(2), T'(2), and T*(2) values decreased with increasing field strength across all investigated brain regions.
- T(2) exhibited a linear dependence on field strength.
Conclusions:
- GESSE is a robust method for quantitative T(2) and T'(2) mapping at 7.0 T.
- Optimized fitting and timing parameters enhance the reliability of T(2) measurements.
- Field-dependent changes in T(2), T'(2), and T*(2) were observed in human brain tissues.
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