On multi-path longitudinal spin relaxation in brain tissue

The purpose of this paper is to confirm previous reports that identified magnetization transfer (MT) as an inherent driver of longitudinal relaxation in brain tissue by asserting a substantial difference between the T(1) relaxation times of the free and the semi-solid spin pools. Further, we aim to identify an avenue towards the quantification of these relaxation processes on a voxel-by-voxel basis in a clinical imaging setting, i.e. with a nominal resolution of 1mm isotropic and full brain coverage in 12min. To this end, we optimized a hybrid-state pulse sequence for mapping the parameters of an unconstrained MT model. We scanned 4 people with relapsing-remitting multiple sclerosis (MS) and 4 healthy controls with this pulse sequence and estimated [Formula: see text] and [Formula: see text] for the free and semi-solid spin pool of healthy WM, respectively, confirming previous reports and questioning the commonly used assumptions [Formula: see text] or [Formula: see text]. Further, we estimated a fractional size of the semi-solid spin pool of [Formula: see text] , which is larger than previously assumed. An analysis of [Formula: see text] in normal appearing white matter revealed statistically significant differences between individuals with MS and controls. In conclusion, we confirm that longitudinal spin relaxation in brain tissue is dominated by MT and that the hybrid state facilitates a voxel-wise fit of the unconstrained MT model, which enables the analysis of subtle neurodegeneration.