Abstract

The absence of nigral hyperintensity is a promising MR marker for Parkinson’s disease (PD), but its small size imposes limitations on its routine use. Our aim was to compare Multi Echo Data Image Combination (MEDIC), segmented echo-planar imaging (EPISEG) and fluid-attenuated inversion recovery (FLAIR) sequences, as well as both magnitude (MAG) and susceptibility-weighted imaging (SWI) reconstructions of single-echo gradient echo for nigral hyperintensity imaging. Twenty-five healthy and twenty PD subjects were included. Sensitivity to motion artefacts, confidence of the radiologist in interpretation, rate of nondiagnostic scans and diagnostic accuracy were assessed. EPISEG was less motion-sensitive than MEDIC, MAG, and SWI, while FLAIR was less motion-sensitive than MAG and SWI. The reviewers were more confident when using EPISEG compared to any other techniques and MEDIC was superior to FLAIR. The proportions of nondiagnostic scans were lower for EPISEG than for other sequences. The best diagnostic performance was achieved for EPISEG (sensitivity = 65%, specificity = 96%). Using EPISEG, the absence of nigral hyperintensity in PD was associated with higher Hoehn-Yahr stage and MDS-UPDRS II + III. Nigral hyperintensity may be intact at the very early stages of PD. The promising properties of EPISEG may help the transfer of nigral hyperintensity imaging into daily clinical practice.

Highlights

  • The absence of nigral hyperintensity is a promising MR marker for Parkinson’s disease (PD), but its small size imposes limitations on its routine use

  • EPISEG was significantly less sensitive to motion compared to Multi Echo Data Image Combination (MEDIC), MAG, and susceptibility-weighted imaging (SWI) techniques

  • The reviewers were more confident in assessing nigral hyperintensity using EPISEG compared to any of the other sequences, and they were more confident when using MEDIC compared to fluid-attenuated inversion recovery (FLAIR)

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Summary

Introduction

The absence of nigral hyperintensity is a promising MR marker for Parkinson’s disease (PD), but its small size imposes limitations on its routine use. By combining 7T MRI and histologic data, Blazejewska et al.[8] found that the oval hyperintense region conforms to nigrosome 1 subregion of substantia nigra, showing severe loss of dopamine-containing neurons in PD Since these pioneering ultra-high field studies, the normal appearance of nigral hyperintensity and its loss in PD have been replicated at 3T field-strength, which is more widely available in clinical p­ ractice[3,6,9,10,11,12,13]. The measurement was aimed to be Scientific Reports | (2021) 11:1179

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