6533b85bfe1ef96bd12bb2d7

RESEARCH PRODUCT

Assessment of cortical damage in early multiple sclerosis with quantitative T 2 relaxometry

Amgad DrobyHilga ZimmermannSarah C. ReitzJohannes C. KleinHelmuth SteinmetzStephanie-michelle HofVinzenz FleischerFrauke ZippRené-maxime GracienRalf Deichmann

subject

Pathologymedicine.medical_specialtyClinically isolated syndromemedicine.diagnostic_testbusiness.industryMultiple sclerosisMagnetic resonance imagingmedicine.disease030218 nuclear medicine & medical imaging03 medical and health sciences0302 clinical medicinemedicine.anatomical_structureCerebral cortexIn vivoRegion of interestCortex (anatomy)medicineMolecular MedicineRadiology Nuclear Medicine and imagingMagnetization transferbusiness030217 neurology & neurosurgerySpectroscopy

description

T2 relaxation time is a quantitative MRI in vivo surrogate of cerebral tissue damage in multiple sclerosis (MS) patients. Cortical T2 prolongation is a known feature in later disease stages, but has not been demonstrated in the cortical normal appearing gray matter (NAGM) in early MS. This study centers on the quantitative evaluation of the tissue parameter T2 in cortical NAGM in a collective of early MS and clinically isolated syndrome (CIS) patients, hypothesizing that T2 prolongation is already present at early disease stages and variable over space, in line with global and focal inflammatory processes in MS. Additionally, magnetization transfer ratio (MTR) mapping was performed for further characterization of the expected cortical T2 alteration. Quantitative T2 and MTR maps were acquired from 12 patients with CIS and early MS, and 12 matched healthy controls. The lesion-free part of the cortical volume was identified, and the mean T2 and MTR values and their standard deviations within the cortical volume were determined. For evaluation of spatial specificity, cortical lobar subregions were tested separately for differences of mean T2 and T2 standard deviation. We detected significantly prolonged T2 in cortical NAGM in patients. T2 prolongation was found across the whole cerebral cortex and in all individual lobar subregions. Significantly higher standard deviations across the respective region of interest were found for the whole cerebral cortex and all subregions, suggesting the occurrence of spatially inhomogeneous cortical damage in all regions studied. A trend was observed for MTR reduction and increased MTR variability across the whole cortex in the MS group, suggesting demyelination. In conclusion, our results suggest that cortical damage in early MS is evidenced by spatially inhomogeneous T2 prolongation which goes beyond demyelination. Iron deposition, which is known to decrease T2, seems less prominent.

https://doi.org/10.1002/nbm.3486