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Published in: Neurological Sciences 6/2022

Open Access 01-06-2022 | Dystonia | Original Article

Uncovering clinical and radiological asymmetry in progressive supranuclear palsy—Richardson’s syndrome

Authors: Marina Picillo, Maria Francesca Tepedino, Filomena Abate, Sara Ponticorvo, Roberto Erro, Sofia Cuoco, Nevra Oksuz, Gianfranco Di Salle, Francesco Di Salle, Fabrizio Esposito, Maria Teresa Pellecchia, Renzo Manara, Paolo Barone

Published in: Neurological Sciences | Issue 6/2022

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Abstract

Background

Richardson’s syndrome (RS) is considered the most symmetric phenotype of progressive supranuclear palsy (PSP) as opposed to PSP with predominant corticobasal syndrome (PSP-CBS) or parkinsonism (PSP-P).

Objectives

Evaluate asymmetrical motor and higher cortical features in probable PSP-RS and compare the degree of asymmetry of cortical lobes and hemispheres between PSP-RS, PSP-CBS, PSP-P, and age-matched healthy controls (HC).

Methods

Asymmetry of motor and higher cortical features evaluated with an extensive videotaped neurologic examination was investigated in 28 PSP-RS, 8 PSP-CBS, and 14 PSP-P. Brain MRI to compute the laterality index (LI) was performed in 36 patients as well as in 56 HC.

Results

In PSP-RS, parkinsonism was the most common asymmetric motor feature (53.6%), followed by dystonia and myoclonus (21.4% and 17.9%, respectively). Among higher cortical features, limb apraxia was found asymmetric in about one-third of patients. PSP-RS disclosed higher LI for hemispheres compared to HC, indicating a greater degree of asymmetry (p = 0.003). The degree of asymmetry of clinical features was not different between PSP-RS and those qualifying for PSP-CBS or PSP-P. As for imaging, LI was not different between PSP-RS, PSP-CBS, and PSP-P in any cortical region.

Conclusions

Motor and higher cortical features are asymmetric in up to 50% of PSP-RS who also present a greater degree of asymmetry in hemispheres compared to age-matched HC. Lateralization of clinical features should be annotated in PSP.
Literature
1.
go back to reference Hoglinger GU, Respondek G, Stamelou M, et al; Movement Disorder Society-endorsed PSP Study Group (2017) Clinical diagnosis of progressive supranuclear palsy: the movement disorder society criteria. Mov Disord 32:853–864. Hoglinger GU, Respondek G, Stamelou M, et al; Movement Disorder Society-endorsed PSP Study Group (2017) Clinical diagnosis of progressive supranuclear palsy: the movement disorder society criteria. Mov Disord 32:853–864.
2.
go back to reference Litvan I, Agid Y, Calne D et al (1996) Clinical reserach criteria for the diagnosis of progressive supranuclear palsy: report of the NINDS-SPSP international workshop. Neurology 47(1):1–9CrossRef Litvan I, Agid Y, Calne D et al (1996) Clinical reserach criteria for the diagnosis of progressive supranuclear palsy: report of the NINDS-SPSP international workshop. Neurology 47(1):1–9CrossRef
3.
go back to reference Litvan I, Mangone CA, McKee A et al (1996) Natural history of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) and clinical predictors of survival: a clinicopathological study. J Neurol Neurosurg Psychiatry 60(6):615–620CrossRef Litvan I, Mangone CA, McKee A et al (1996) Natural history of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) and clinical predictors of survival: a clinicopathological study. J Neurol Neurosurg Psychiatry 60(6):615–620CrossRef
4.
go back to reference Respondek G, Hoglinger GU. (2016) The phenotypic spectrum of progressive supranuclear palsy. 22Suppl1:S34–36. Respondek G, Hoglinger GU. (2016) The phenotypic spectrum of progressive supranuclear palsy. 22Suppl1:S34–36.
5.
go back to reference Grimm MJ, Respondek G, Stamelou M, et al; Movement Disorder Society-endorsed PSP Study Group. (2019) How to apply the movement disorder society criteria for diagnosis of progressive supranuclear palsy. Mov Disord 34:1228–1232. Grimm MJ, Respondek G, Stamelou M, et al; Movement Disorder Society-endorsed PSP Study Group. (2019) How to apply the movement disorder society criteria for diagnosis of progressive supranuclear palsy. Mov Disord 34:1228–1232.
6.
go back to reference Picillo M, Cuoco S, Tepedino MF,: Salerno PSP study group, et al (2019) Motor, cognitive and behavioral differences in MDS PSP phenotypes. J Neurol 266:1727–1735CrossRef Picillo M, Cuoco S, Tepedino MF,: Salerno PSP study group, et al (2019) Motor, cognitive and behavioral differences in MDS PSP phenotypes. J Neurol 266:1727–1735CrossRef
7.
go back to reference Stezin A, Holla VV, Chaithra SP et al (2019) Asymmetric limb dystonia in progressive supranuclear palsy: conundrum in nosology. Movement Disorders Clinical Practice 6:415–416CrossRef Stezin A, Holla VV, Chaithra SP et al (2019) Asymmetric limb dystonia in progressive supranuclear palsy: conundrum in nosology. Movement Disorders Clinical Practice 6:415–416CrossRef
8.
go back to reference Bayram E, Dickson D, Reich S, Litvan I (2020) Pathology-proven corticobasal degeneration presenting as Richardson’s syndrome. Mov Disord Clin Pract 7:267–272CrossRef Bayram E, Dickson D, Reich S, Litvan I (2020) Pathology-proven corticobasal degeneration presenting as Richardson’s syndrome. Mov Disord Clin Pract 7:267–272CrossRef
9.
go back to reference Oide T, Ohara S, Yazawa M et al (2002) Progressive supranuclear palsy with asymmetric tau pathology presenting with unilateral limb dystonia. Acta Neuropathol 104:209–214CrossRef Oide T, Ohara S, Yazawa M et al (2002) Progressive supranuclear palsy with asymmetric tau pathology presenting with unilateral limb dystonia. Acta Neuropathol 104:209–214CrossRef
10.
go back to reference Golbe LI, Ohman-Strickland PA (2007) A clinical rating scale for progressive supranuclear palsy. Brain 130:1552–1565CrossRef Golbe LI, Ohman-Strickland PA (2007) A clinical rating scale for progressive supranuclear palsy. Brain 130:1552–1565CrossRef
11.
go back to reference Picillo M, Erro R, Cuoco S,: PSP Salerno study group, et al (2018) MDS PSP criteria in real-life clinical setting: motor and cognitive characterization of subtypes. Mov Disord 33:1361–1365CrossRef Picillo M, Erro R, Cuoco S,: PSP Salerno study group, et al (2018) MDS PSP criteria in real-life clinical setting: motor and cognitive characterization of subtypes. Mov Disord 33:1361–1365CrossRef
12.
go back to reference Picillo M, Tepedino MF, Abate F et al (2020) Midbrain MRI assessments in progressive supranuclear palsy subtypes. J Neurol Neurosurg Psychiatry 91:98–103CrossRef Picillo M, Tepedino MF, Abate F et al (2020) Midbrain MRI assessments in progressive supranuclear palsy subtypes. J Neurol Neurosurg Psychiatry 91:98–103CrossRef
13.
go back to reference Picillo M, Abate F, Ponticorvo S, et al (2020) Association of MRI measures with disease severity and progression in progressive supranuclear palsy. Front Neurol 11:603161. Picillo M, Abate F, Ponticorvo S, et al (2020) Association of MRI measures with disease severity and progression in progressive supranuclear palsy. Front Neurol 11:603161.
14.
go back to reference Payan CA, Viallet F, Landwehrmeyer BG et al (2011) NNIPPS Study Group. Disease severity and progression in progressive supranuclear palsy and multiple system atrophy: validation of the NNIPPS–Parkinson Plus Scale. PLoS One 6(8):e22293. Payan CA, Viallet F, Landwehrmeyer BG et al (2011) NNIPPS Study Group. Disease severity and progression in progressive supranuclear palsy and multiple system atrophy: validation of the NNIPPS–Parkinson Plus Scale. PLoS One 6(8):e22293.
15.
go back to reference De Renzi E, Motti F, Nichelli P. (1980) Imitating gestures. A quantitative approach to ideomotor apraxia. Arch Neurol 37(1):6–10. De Renzi E, Motti F, Nichelli P. (1980) Imitating gestures. A quantitative approach to ideomotor apraxia. Arch Neurol 37(1):6–10.
16.
go back to reference Dale AM, Sereno MI (1993) Improved localization of cortical activity by combining EEG and MEG with MRI cortical surface reconstruction: a linear approach. J Cogn Neurosci 5(2):162–176CrossRef Dale AM, Sereno MI (1993) Improved localization of cortical activity by combining EEG and MEG with MRI cortical surface reconstruction: a linear approach. J Cogn Neurosci 5(2):162–176CrossRef
17.
go back to reference Desikan RS, Ségonne F, Fischl B et al (2006) An automated labeling system for subdividing the human cerebral cortex on MRI scans into gyral based regions of interest. Neuroimage 31(31):968–980CrossRef Desikan RS, Ségonne F, Fischl B et al (2006) An automated labeling system for subdividing the human cerebral cortex on MRI scans into gyral based regions of interest. Neuroimage 31(31):968–980CrossRef
18.
go back to reference Piot I, Schweyer L, Respondek G et al (2020) The Progressive Supranuclear Palsy Clinical Deficits Scale. Mov Disord 35:650–651CrossRef Piot I, Schweyer L, Respondek G et al (2020) The Progressive Supranuclear Palsy Clinical Deficits Scale. Mov Disord 35:650–651CrossRef
Metadata
Title
Uncovering clinical and radiological asymmetry in progressive supranuclear palsy—Richardson’s syndrome
Authors
Marina Picillo
Maria Francesca Tepedino
Filomena Abate
Sara Ponticorvo
Roberto Erro
Sofia Cuoco
Nevra Oksuz
Gianfranco Di Salle
Francesco Di Salle
Fabrizio Esposito
Maria Teresa Pellecchia
Renzo Manara
Paolo Barone
Publication date
01-06-2022
Publisher
Springer International Publishing
Published in
Neurological Sciences / Issue 6/2022
Print ISSN: 1590-1874
Electronic ISSN: 1590-3478
DOI
https://doi.org/10.1007/s10072-022-05919-x

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