Midbrain MRI assessments in progressive supranuclear palsy subtypes

Marina Picillo, Maria Francesca Tepedino, Filomena Abate, Roberto Erro, Sara Ponticorvo, Salvatore Tartaglione, Giampiero Volpe, Daniela Frosini, Paolo Cecchi, Mirco Cosottini, Roberto Ceravolo, Fabrizio Esposito, Maria Teresa Pellecchia, Paolo Barone, Renzo Manara

Research output: Contribution to journalArticlepeer-review

38 Scopus citations

Abstract

Objectives To explore the role of the available midbrain-based MRI morphometric assessments in (1) differentiating among progressive supranuclear palsy (PSP) subtypes (PSP Richardson's syndrome (PSP-RS), PSP with predominant parkinsonism (PSP-P) and the other variant syndromes of PSP (vPSP)), and (2) supporting the diagnosis of PSP subtypes compared with Parkinson's disease (PD) and healthy controls (HC). Methods Seventy-eight patients with PSP (38 PSP-RS, 21 PSP-P and 19 vPSP), 35 PD and 38 HC were included in the present analysis. Available midbrain-based MRI morphometric assessments were calculated for all participants. Results Current MRI midbrain-based assessments do not display an adequate sensitivity and specificity profile in differentiating PSP subtypes. On the other hand, we confirmed MR Parkinsonism Index (MRPI) and pons area to midbrain area ratio (P/M) have adequate diagnostic value to support PSP-RS clinical diagnosis compared with both PD and HC, but low sensitivity and specificity profile in differentiating PSP-P from PD as well as from HC. The same measures show acceptable sensitivity and specificity profile in supporting clinical diagnosis of vPSP versus HC but not versus PD. Similar findings were detected for the newer MRPI and P/M versions. Conclusions Further studies are warranted to identify neuroimaging biomarkers supporting the clinical phenotypic categorisation of patients with PSP. MRPI and P/M have diagnostic value in supporting the clinical diagnosis of PSP-RS. Classification of evidence This study provides class III evidence that available MRI midbrain-based assessments do not have diagnostic value in differentiating the Movement Disorder Society PSP subtypes.

Original languageEnglish (US)
Pages (from-to)98-103
Number of pages6
JournalJournal of Neurology, Neurosurgery and Psychiatry
Volume91
Issue number1
DOIs
StatePublished - Jan 1 2020
Externally publishedYes

Bibliographical note

Publisher Copyright:
© Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.

Keywords

  • Diagnostic criteria
  • Imaging
  • Progressive supranuclear palsy
  • Subtypes

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