Abstract

Background. Magnetic Resonance (MR) diffusion tensor imaging (DTI) is able to quantify in vivo tissue microstructure properties and to detect disease related pathology of the central nervous system. Nevertheless, DTI is limited by low spatial resolution associated with its low signal-to-noise-ratio (SNR). Aim. The aim is to select a DTI sequence for brain clinical studies, optimizing SNR and resolution. Methods and Results. We applied 6 methods for SNR computation in 26 DTI sequences with different parameters using 4 healthy volunteers (HV). We choosed two DTI sequences for their high SNR, they differed by voxel size and b-value. Subsequently, the two selected sequences were acquired from 30 multiple sclerosis (MS) patients with different disability and lesion load and 18 age matched HV. We observed high concordance between mean diffusivity (MD) and fractional anysotropy (FA), nonetheless the DTI sequence with smaller voxel size displayed a better correlation with disease progression, despite a slightly lower SNR. The reliability of corpus callosum (CC) fiber tracking with the chosen DTI sequences was also tested. Conclusions. The sensitivity of DTI-derived indices to MS-related tissue abnormalities indicates that the optimized sequence may be a powerful tool in studies aimed at monitoring the disease course and severity.

Highlights

  • Magnetic Resonance (MR) diffusion tensor imaging (DTI) allows in vivo examination of the tissue microstructure, obtained by exploiting the properties of water diffusion

  • A similar representation was done for sequences with the same parameters but the bvalue, giving the result of SNR decreasing with the increasing of the diffusion-sensitivity coefficient, in particular the SNR estimated on images obtained from sequences with b-value of 1500 s/mm2 was 20% less than the SNR of sequences with b-value of 1000 s/mm2

  • The same analysis confirmed that the minimum TE feasible for the MR-scanner had to be selected, as expected, since DTI is T2 weighted

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Summary

Introduction

Magnetic Resonance (MR) diffusion tensor imaging (DTI) allows in vivo examination of the tissue microstructure, obtained by exploiting the properties of water diffusion. Magnetic Resonance (MR) diffusion tensor imaging (DTI) is able to quantify in vivo tissue microstructure properties and to detect disease related pathology of the central nervous system. Aim. The aim is to select a DTI sequence for brain clinical studies, optimizing SNR and resolution. We applied 6 methods for SNR computation in 26 DTI sequences with different parameters using 4 healthy volunteers (HV). We choosed two DTI sequences for their high SNR, they differed by voxel size and b-value. We observed high concordance between mean diffusivity (MD) and fractional anysotropy (FA), the DTI sequence with smaller voxel size displayed a better correlation with disease progression, despite a slightly lower SNR. The sensitivity of DTI-derived indices to MS-related tissue abnormalities indicates that the optimized sequence may be a powerful tool in studies aimed at monitoring the disease course and severity

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