Abstract

We investigated the association between the Magnetic Resonance Parkinsonism Index (MRPI) and REM sleep behavior disorder (RBD). We included 226 de novo PD patients (82 PD-RBD and 144 PD-noRBD) and 19 idiopathic RBD patients. Furthermore, 3T T1-weighted MR images were used for automated brainstem calculations. MRPI values were higher in the PD-RBD (p = 0.004) compared to PD-noRBD patients. Moreover, MRPI proved to be a significant predictor of REM Behavior Disorder Screening Questionnaire scores in PD (β = 0.195, p = 0.007) and iRBD patients (β = 0.582, p = 0.003). MRPI can be used as an imaging marker of RBD in patients with de novo PD and iRBD.

Highlights

  • REM sleep behavior disorder (RBD) is characterized by loss of physiological muscle atonia and episodes of dream-enactment behaviors during REM sleep [1]

  • We investigated whether the Magnetic Resonance Parkinsonism Index (MRPI) could represent a useful neuroimaging marker able to capture the morphometric changes of brainstem subregions associated with RBD in de novo patients with PD and subjects with Idiopathic RBD (iRBD)

  • A total of 82 PD patients were classified as PD-RBD while 144 were classified as PD-noRBD

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Summary

Introduction

REM sleep behavior disorder (RBD) is characterized by loss of physiological muscle atonia and episodes of dream-enactment behaviors during REM sleep [1]. RBD’s pathophysiology has not been completely elucidated, lesions in the brainstem structures, such as midbrain, pons, and medulla,- have been associated with RBD in both animal [5,6] and human studies [7]. The Magnetic Resonance Parkinsonism Index (MRPI), which integrates the pons and midbrain areas and the width of middle and superior cerebellar peduncles, has been proven to be a measure to capture the midbrain and superior cerebellar peduncles atrophy, characterizing patients with progressive supranuclear palsy [13,14]. We investigated whether the MRPI could represent a useful neuroimaging marker able to capture the morphometric changes of brainstem subregions associated with RBD in de novo patients with PD and subjects with iRBD

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