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Updated: Mar 2, 2026

Whole-brain Segmentation and Change-point Analysis of Anatomical Brain MRI—Application in Premanifest Huntington's Disease
Published on: June 9, 2018
Cerebellar Gray Matter Alterations in Huntington Disease: A Voxel-Based Morphometry Study
Paula C de Azevedo1,2, Rachel P Guimarães3, Camila C Piccinin3
1Neuroimaging Laboratory, University of Campinas UNICAMP, Campinas, Rua Vital Brasil, 251, Cidade Universitária Zeferino Vaz, Campinas, SP, 13083-887, Brazil. paulacazevedo@yahoo.com.br.
Huntington disease (HD) involves cerebellar gray matter (GM) changes, particularly in the anterior and posterior regions. These alterations correlate with motor and cognitive symptoms, highlighting the cerebellum's role in HD.
Area of Science:
- Neuroscience
- Neurology
- Neuroimaging
Background:
- Previous neuropathological and neuroimaging studies suggest cerebellar involvement in Huntington disease (HD).
- A detailed in vivo evaluation of cerebellar morphology in HD is crucial for understanding disease mechanisms.
Purpose of the Study:
- To conduct a comprehensive assessment of cerebellar gray matter (GM) morphology in individuals with Huntington disease (HD).
- To investigate the correlation between cerebellar GM alterations and clinical/cognitive measures in HD patients.
Main Methods:
- Utilized the Spatially Unbiased Atlas Template (SUIT)-SPM-toolbox for detailed analysis of cerebellar GM.
- Performed Unified Huntington's Disease Rating Scale (UHDRS) and Montreal Cognitive Assessment (MOCA) on 26 HD patients and 26 controls.
- Employed two-sample t-tests to compare GM density between groups and correlation analyses, corrected for relevant covariates.
Main Results:
- Observed increased cerebellar GM density in the anterior cerebellum in HD patients compared to controls.
- Found significant correlations between GM density in the postero-superior cerebellum and mood symptoms.
- Worse motor function and better cognitive function in HD patients correlated with GM changes in the posterior cerebellum (FDR corrected, p < 0.05).
Conclusions:
- The study demonstrates significant in vivo cerebellar GM changes in individuals with Huntington disease.
- Observed GM alterations are localized to regions involved in sensorimotor integration, motor planning, and emotional processing.
- These findings support a critical role for the cerebellum in the neuropathological progression of Huntington disease.
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