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.

Insights

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.

Related Concept Videos

Cerebellum: Anatomical Regions01:17

Cerebellum: Anatomical Regions

The cerebellum, also known as the "little brain," is located in the posterior cranial fossa, inferior to the tentorium cerebelli and dorsal to the brainstem. It plays a significant role in motor control, coordination, and proprioception.
Cerebellar Structure
Externally, the cerebellum features a highly convoluted surface with numerous folia (narrow ridges) separated by shallow sulci (grooves). The cerebellum is divided into two hemispheres by a thin median structure known as the vermis. The...
5.1K
Cerebrum: Anatomical Overview II01:11

Cerebrum: Anatomical Overview II

Each cerebral hemisphere can be divided into three main regions. The outermost region, the cerebral cortex, is a thin layer (2 to 4 millimeters thick) made up of gray matter, consisting of neuron cell bodies, dendrites, glial cells, and blood vessels. The middle region, or white matter, is primarily composed of myelinated nerve fibers organized into three types of large tracts: association fibers, commissures, and projection fibers. Association fibers connect different areas within the same...
5.4K
Alzheimer's Disease: Overview01:26

Alzheimer's Disease: Overview

Alzheimer's Disease (AD) is a continually advancing neurodegenerative disorder, distinguished by escalating memory loss, cognitive dysfunction, and dementia. The disease unfolds in three stages: preclinical, mild cognitive impairment (MCI), and dementia. Its onset is insidious, and the progression gradual, with the cause not well explained by other disorders.
The clinical diagnosis of AD hinges on the presence of memory and other cognitive impairments. Biomarkers, such as changes in Aβ...
1.9K