Abstract

Fractional anisotropy (FA) is the most commonly used quantitative measure of diffusion in the brain. Changes in FA have been reported in many neurological disorders, but the implementation of diffusion tensor imaging (DTI) in daily clinical practice remains challenging. We propose a novel color look-up table (LUT) based on normative data as a tool for screening FA changes. FA was calculated for 76 healthy volunteers using 12 motion-probing gradient directions (MPG), a subset of 59 subjects was additionally scanned using 30 MPG. Population means and 95% prediction intervals for FA in the corpus callosum, frontal gray matter, thalamus and basal ganglia were used to create the LUT. Unique colors were assigned to inflection points with continuous ramps between them. Clinical use was demonstrated on 17 multiple system atrophy (MSA) patients compared to 13 patients with Parkinson disease (PD) and 17 healthy subjects. Four blinded radiologists classified subjects as MSA/non-MSA. Using only the LUT, high sensitivity (80%) and specificity (84%) were achieved in differentiating MSA subjects from PD subjects and controls. The LUTs generated from 12 and 30 MPG were comparable and accentuate FA abnormalities.

Highlights

  • Radiologists primarily make clinical decisions based on the qualitative assessment of images

  • Generation of the look-up table (LUT) A nonlinear LUT was created using inflection points based on fractional anisotropy (FA) values in the basal ganglia (BG), GM and corpus callosum (CC)

  • The mean FA of white matter region of interest (ROI) was equal in both sequences, while FA values in the BG and GM differed

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Summary

Introduction

Radiologists primarily make clinical decisions based on the qualitative assessment of images. A general impression may be followed by measurements of size (e.g., of a solid tumor), quantitative tissue measures (e.g., apparent diffusion coefficient in acute stroke) or by more complex post-processing (e.g., in cardiac magnetic resonance imaging). Despite the fact that the Hounsfield unit (based on the amount of X-radiation absorbed by tissue, used in computed tomography) is no longer the only absolute voxel intensity measure and widespread film-less radiology enables comparison of quantitative parameters with previous records, voxel value measurements in magnetic resonance imaging (MRI) remain uncommon. Diffusion tensor imaging (DTI) has become a useful quantitative tool in experimental medicine for investigating certain morphological and functional characteristics of the brain in both health and disease states [1,2,3]. In some diseases typically affecting the white matter of the brain, DTI may improve the diagnostic process [4] and has shown utility in monitoring disease progression [5,6,7]

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