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Brain gray matter abnormalities in progressive supranuclear palsy revisited
PingLei Pan1,2, Yi Liu1,3,4,5,6, Yang Zhang1,3,4,5,6
1Department of Neurology, Drum Tower Hospital, Medical School of Nanjing University, Nanjing, PR China.
Progressive supranuclear palsy (PSP) patients show widespread gray matter (GM) loss in cortical and subcortical brain regions. This meta-analysis reveals a specific pattern of GM atrophy linked to PSP symptoms.
Area of Science:
- Neuroimaging
- Neurology
- Neurodegeneration
Background:
- Voxel-based morphometry (VBM) studies on progressive supranuclear palsy (PSP) report inconsistent gray matter (GM) abnormalities.
- Understanding the precise neuroanatomical changes in PSP is crucial for diagnosis and treatment.
Purpose of the Study:
- To identify consistent patterns of GM anomalies in PSP using a coordinate-based meta-analytic approach.
- To explore potential confounding factors contributing to heterogeneity in VBM studies of PSP.
Main Methods:
- A coordinate-based meta-analysis using Seed-based d Mapping was performed.
- Included 18 VBM studies with 284 PSP patients and 367 healthy controls.
- Analyzed data from published VBM studies on PSP.
Main Results:
- Significant GM reductions were observed in PSP patients compared to controls.
- Affected regions include frontal cortices, insula, striatum, thalamus, midbrain, and cerebellum.
- Identified a specific neuroanatomical pattern of GM atrophy in PSP.
Conclusions:
- PSP is characterized by widespread cortical-subcortical GM atrophy.
- This pattern correlates with key PSP clinical features like gaze palsy and motor deficits.
- Future research should account for confounding factors to reduce heterogeneity.
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