Abstract

ObjectivesTo evaluate the microstructural damage in the heterogeneity of different white matter areas in relapsing-remitting multiple sclerosis (RRMS) patients by using diffusion kurtosis imaging (DKI) and its correlation with clinical and cognitive status.Materials and MethodsKurtosis fractional anisotropy (KFA), fractional anisotropy (FA), mean kurtosis (MK), and mean diffusivity (MD) in T1-hypointense lesions (T1Ls), pure T2-hyperintense lesions (pure-T2Ls), normal-appearing white matter (NAWM), and white matter in healthy controls (WM in HCs) were measured in 48 RRMS patients and 26 sex- and age-matched HCs. All the participants were assessed with the Mini-Mental State Examination (MMSE), the Montreal Cognitive Assessment (MoCA), and the Symbol Digit Modalities Test (SDMT) scores as the cognitive status. The Kurtzke Expanded Disability Status Scale (EDSS) scores were used to evaluate the clinical status in RRMS patients.ResultsThe lowest KFA, FA, and MK values and the highest MD values were found in T1Ls, followed by pure-T2Ls, NAWM, and WM in HCs. The T1Ls and pure-T2Ls were significantly different in FA (p = 0.002) and MK (p = 0.013), while the NAWM and WM in HCs were significantly different in KFA, FA, and MK (p < 0.001; p < 0.001; p = 0.001). The KFA, FA, MK, and MD values in NAWM (r = 0.360, p = 0.014; r = 0.415, p = 0.004; r = 0.369, p = 0.012; r = −0.531, p < 0.001) were correlated with the MMSE scores and the FA, MK, and MD values in NAWM (r = 0.423, p = 0.003; r = 0.427, p = 0.003; r = −0.359, p = 0.014) were correlated with the SDMT scores.ConclusionApplying DKI to the imaging-based white matter classification has the potential to reflect the white matter damage and is correlated with cognitive impairment.

Highlights

  • Multiple sclerosis (MS) is one of the most prevalent chronic inflammatory demyelinated diseases, which is characterized by edema, inflammation, demyelination, and axonal loss in the central nervous system (Evangelou et al, 2000; Reich et al, 2018)

  • We found the lowest kurtosis fractional anisotropy (KFA), fractional anisotropy (FA), and mean kurtosis (MK) values, respectively, in T1-hypointense lesions (T1Ls), followed by pureT2Ls, normal-appearing white matter (NAWM), and white matter (WM) in healthy controls (HCs)

  • NAWM was significantly different from WM in HCs, even if it had minor histopathological damage compared to focal lesions

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Summary

Introduction

Multiple sclerosis (MS) is one of the most prevalent chronic inflammatory demyelinated diseases, which is characterized by edema, inflammation, demyelination, and axonal loss in the central nervous system (Evangelou et al, 2000; Reich et al, 2018). White matter lesions (WMLs) can be detected as areas of hyperintensity on T2-weighted images (T2WI) or fluid-attenuated inversion recovery (FLAIR) images. Those T2-hyperintense lesions (T2Ls) correspond to a broad spectrum of pathological changes, including edema, inflammation, demyelination, remyelination, gliosis, liquid necrosis, and axonal loss (MacKay et al, 2006). We hypothesize that those differences in intensities of WMLs on T1-weighted images (T1WI) and T2WI/FLAIR represent the different pathological changes in the white matter, which contribute differently to the progression of the disease

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