Impact of Magnetic Resonance Imaging Markers on the Diagnostic Performance of the International Parkinson and Movement Disorder Society Multiple System Atrophy Criteria

  • Ida Jensen
  • , Johanne Heine
  • , Viktoria C. Ruf
  • , Yaroslau Compta
  • , Laura Molina Porcel
  • , Claire Troakes
  • , Albert Vamanu
  • , Sophia Downes
  • , David Irwin
  • , Jesse Cohen
  • , Edward B. Lee
  • , Christer Nilsson
  • , Elisabet Englund
  • , Mojtaba Nemati
  • , Sabrina Katzdobler
  • , Johannes Levin
  • , Alex Pantelyat
  • , Joseph Seemiller
  • , Stephen Berger
  • , John van Swieten
  • Elise Dopper, Annemieke Rozenmuller, Gabor G. Kovacs, Nathaniel Bendahan, Anthony E. Lang, Jochen Herms, Günter Höglinger, Franziska Hopfner

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

Background: Multiple system atrophy is a neurodegenerative disease with α-synuclein aggregation in glial cytoplasmic inclusions, leading to dysautonomia, parkinsonism, and cerebellar ataxia. Objective: The aim of this study was to validate the accuracy of the International Parkinson and Movement Disorder Society Multiple System Atrophy clinical diagnostic criteria, particularly considering the impact of the newly introduced brain magnetic resonance imaging (MRI) markers. Methods: Diagnostic accuracy of the clinical diagnostic criteria for multiple system atrophy was estimated retrospectively in autopsy-confirmed patients with multiple system atrophy, Parkinson's disease, progressive supranuclear palsy, and corticobasal degeneration. Results: We identified a total of 240 patients. Sensitivity of the clinically probable criteria was moderate at symptom onset but improved with disease duration (year 1: 9%, year 3: 39%, final ante mortem record: 77%), whereas their specificity remained consistently high (99%–100% throughout). Sensitivity of the clinically established criteria was low during the first 3 years (1%–9%), with mild improvement at the final ante mortem record (22%), whereas specificity remained high (99%–100% throughout). When MRI features were excluded from the clinically established criteria, their sensitivity increased considerably (year 1: 3%, year 3: 22%, final ante mortem record: 48%), and their specificity was not compromised (99%–100% throughout). Conclusions: The International Parkinson and Movement Disorder Society multiple system atrophy diagnostic criteria showed consistently high specificity and low to moderate sensitivity throughout the disease course. The MRI markers for the clinically established criteria reduced their sensitivity without improving specificity. Combining clinically probable and clinically established criteria, but disregarding MRI features, yielded the best sensitivity with excellent specificity and may be most appropriate to select patients for therapeutic trials.

Original languageEnglish (US)
Pages (from-to)1514-1522
Number of pages9
JournalMovement Disorders
Volume39
Issue number9
DOIs
StatePublished - Sep 2024

All Science Journal Classification (ASJC) codes

  • Neurology
  • Clinical Neurology

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