Intra-voxel and inter-voxel coherence in patients with multiple sclerosis assessed using diffusion tensor MRI

Abstract.

Previous diffusion tensor magnetic resonance imaging (DT-MRI) studies reported mean diffusivity (${\overline D}$) and fractional anisotropy (FA) changes in lesions and normal-appearing white matter (NAWM) of patients with multiple sclerosis (MS), but neglected the additional information which can be obtained by the analysis of the inter-voxel coherence (C). The present study is based on a large sample of patients with MS and it is aimed at assessing the potential role of C in the quantification of MS-related tissue damage of T2-visible lesions and NAWM. We obtained dual-echo, T1-weighted and DT-MRI scans from 78 patients with relapsing-remitting (RR), secondary progressive (SP), or primary progressive (PP) MS and from 26 healthy volunteers. We calculated ${\overline D}$, FA and C of T2-hyperintense lesions, T1-isointense lesions, T1-hypointense lesions and several areas of the NAWM. ${\overline D}$ and FA of the majority of NAWM regions studied from MS patients were different from the corresponding quantities of the white matter from controls. NAWM C from patients was lower than white matter C from controls only for the parietal pericallosal areas. SPMS patients had higher corpus callosum ${\overline D}$ and lower corpus callosum FA and C than patients with either RRMS or PPMS. Average lesion ${\overline D}$ was higher, and average FA and C lower than the corresponding quantities measured in the NAWM. Average T1-hypointense lesion ${\overline D}$ was higher and average FA lower than the corresponding quantities of T1-isointense lesions, whereas average C of these two lesion populations were not different. SPMS had higher average lesion ${\overline D}$ than both PPMS and RRMS patients. NAWM ${\overline D}$ and C of the corpus callosum were moderately correlated with disability. This study confirms the role of DT-MRI metrics to identify MS lesions with different amounts of tissue damage and to detect diffuse changes in the NAWM. It also shows that measuring C enables us to obtain additional information about tissue damage, which is complementary to that given by the analysis of ${\overline D}$ and FA.