» Articles » PMID: 37330976

Brain FDG-PET Correlates of Saccadic Disorders in Early PSP

Overview
Journal J Neurol
Specialty Neurology
Date 2023 Jun 18
PMID 37330976
Authors
Affiliations
Soon will be listed here.
Abstract

Background: New diagnostic criteria of Progressive Supranuclear Palsy (PSP) have highlighted the interest of Eye Movement Records (EMR) at the early stage of the disease.

Objectives: To investigate the metabolic brain correlates of ocular motor dysfunction using [18F] Fluorodeoxyglucose Positron Emission Tomography (FDG-PET) in early PSP.

Methods: Retrospective observational descriptive study on longitudinal data with patients who underwent EMR and FDG-PET at the stage of suggestive and possible PSP according to Movement Disorders Society criteria. Longitudinal follow-up enables to confirm diagnosis of probable PSP. Using the Statistical Parametric Mapping software, we performed whole-brain voxel-based correlations between oculomotor variables and FDG-PET metabolism.

Results: Thirty-seven patients with early PSP who fulfilled criteria of probable PSP during the follow-up were included. Decrease in the gain of vertical saccades correlated with reduced metabolism in Superior Colliculi (SC). We also found a positive correlation between mean velocity of horizontal saccades and SC metabolism as well as dorsal nuclei in the pons. Finally, increase in horizontal saccades latencies correlated with decrease of posterior parietal metabolism.

Conclusions: These findings suggest the early involvement of SC in saccadic dysfunction in the course of PSP.

Citing Articles

Systematic assessment of square-wave jerks in progressive supranuclear palsy: a video-oculographic study.

Facchin A, Buonocore J, Crasa M, Quattrone A, Quattrone A J Neurol. 2024; 271(10):6639-6646.

PMID: 39134726 PMC: 11447104. DOI: 10.1007/s00415-024-12617-5.


Patterns of brain volume and metabolism predict clinical features in the progressive supranuclear palsy spectrum.

Ali F, Clark H, Machulda M, Senjem M, Lowe V, Jack Jr C Brain Commun. 2024; 6(4):fcae233.

PMID: 39056025 PMC: 11272075. DOI: 10.1093/braincomms/fcae233.


New Perspectives in Radiological and Radiopharmaceutical Hybrid Imaging in Progressive Supranuclear Palsy: A Systematic Review.

Strobel J, Muller H, Ludolph A, Beer A, Sollmann N, Kassubek J Cells. 2023; 12(24).

PMID: 38132096 PMC: 10742083. DOI: 10.3390/cells12242776.

References
1.
Litvan I, Agid Y, Calne D, Campbell G, Dubois B, Duvoisin R . Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of the NINDS-SPSP international workshop. Neurology. 1996; 47(1):1-9. DOI: 10.1212/wnl.47.1.1. View

2.
Steele J, Richardson J, Olszewski J . PROGRESSIVE SUPRANUCLEAR PALSY. A HETEROGENEOUS DEGENERATION INVOLVING THE BRAIN STEM, BASAL GANGLIA AND CEREBELLUM WITH VERTICAL GAZE AND PSEUDOBULBAR PALSY, NUCHAL DYSTONIA AND DEMENTIA. Arch Neurol. 1964; 10:333-59. DOI: 10.1001/archneur.1964.00460160003001. View

3.
Respondek G, Kurz C, Arzberger T, Compta Y, Englund E, Ferguson L . Which ante mortem clinical features predict progressive supranuclear palsy pathology?. Mov Disord. 2017; 32(7):995-1005. PMC: 5543934. DOI: 10.1002/mds.27034. View

4.
Respondek G, Stamelou M, Kurz C, Ferguson L, Rajput A, Chiu W . The phenotypic spectrum of progressive supranuclear palsy: a retrospective multicenter study of 100 definite cases. Mov Disord. 2014; 29(14):1758-66. DOI: 10.1002/mds.26054. View

5.
Marx S, Respondek G, Stamelou M, Dowiasch S, Stoll J, Bremmer F . Validation of mobile eye-tracking as novel and efficient means for differentiating progressive supranuclear palsy from Parkinson's disease. Front Behav Neurosci. 2012; 6:88. PMC: 3521127. DOI: 10.3389/fnbeh.2012.00088. View