Midbrain MRI assessments in progressive supranuclear palsy subtypes.
Aged
Aged, 80 and over
Diagnosis, Differential
Female
Humans
Image Processing, Computer-Assisted
Magnetic Resonance Imaging
/ methods
Male
Mesencephalon
/ diagnostic imaging
Middle Aged
Neuroimaging
Parkinsonian Disorders
/ diagnostic imaging
Pons
/ diagnostic imaging
Reproducibility of Results
Sensitivity and Specificity
Supranuclear Palsy, Progressive
/ classification
diagnostic criteria
imaging
progressive supranuclear palsy
subtypes
Journal
Journal of neurology, neurosurgery, and psychiatry
ISSN: 1468-330X
Titre abrégé: J Neurol Neurosurg Psychiatry
Pays: England
ID NLM: 2985191R
Informations de publication
Date de publication:
01 2020
01 2020
Historique:
received:
05
06
2019
revised:
22
07
2019
accepted:
19
08
2019
pubmed:
19
9
2019
medline:
7
7
2020
entrez:
19
9
2019
Statut:
ppublish
Résumé
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). 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. 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. 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. 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.
Identifiants
pubmed: 31527182
pii: jnnp-2019-321354
doi: 10.1136/jnnp-2019-321354
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
98-103Informations de copyright
© Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: None declared.