Progressive gray matter atrophy in parkinsonian variant of multiple system atrophy assessed by using causal

Tong Wu1, Yuanyuan Zhang2,3, Kun Xia3

  • 1Department of Neurology, The Second Affiliated Hospital of Anhui Medical University, Hefei, 230601, China.

Neuroradiology
|September 2, 2024
PubMed
Abstract

Insights

Multiple system atrophy parkinsonian (MSA-P) causes progressive gray matter loss, originating in the right cerebellum and spreading to other brain regions. The cerebellum acts as a key hub, influencing motor and non-motor pathways.

Area of Science:

  • Neuroscience
  • Neurology
  • Radiology

Background:

  • Multiple system atrophy (MSA) is a rare neurodegenerative disorder.
  • Brain morphological alterations are common in MSA.
  • Causal relationships of progressive gray matter atrophy in the MSA parkinsonian (MSA-P) subtype are not well understood.

Purpose of the Study:

  • To investigate the causal relationships between progressive gray matter atrophy in MSA-P patients.
  • To identify the origin and progression patterns of brain structural changes in MSA-P.

Main Methods:

  • Thirty-five MSA-P patients and 35 healthy controls (HC) underwent T1-weighted structural MRI.
  • Voxel-based morphometry and causal structural covariance network (CaSCN) analysis were performed.

Main Results:

  • Gray matter reduction initiated in the right cerebellum and spread to involve numerous brain regions including the cerebellum, basal ganglia, temporal lobe, and frontal lobe with disease duration.
  • The right cerebellum was identified as the core node, projecting causal effects to the bilateral cerebellum, caudate nucleus, and left inferior parietal lobule (IPL).

Conclusions:

  • MSA-P is characterized by progressive gray matter atrophy with the right cerebellum as a probable primary hub.
  • Early cerebellar structural vulnerability in MSA-P may significantly impact motor and non-motor circuits.