Neuropsychological and brain volume differences in patients with left- and right-beginning corticobasal syndrome

PLoS One. 2014 Oct 30;9(10):e110326. doi: 10.1371/journal.pone.0110326. eCollection 2014.

Abstract

Background: Corticobasal Syndrome (CBS) is a rare neurodegenerative syndrome characterized by unilaterally beginning frontoparietal and basal ganglia atrophy. The study aimed to prove the hypothesis that there are differences in hemispheric susceptibility to disease-related changes.

Methods: Two groups of CBS patients with symptoms starting either on the left or right body side were investigated. Groups consisted of four patients each and were matched for sex, age and disease duration. Patient groups and a group of eight healthy age-matched controls were analyzed using deformation field morphometry and neuropsychological testing. To further characterize individual disease progression regarding brain atrophy and neuropsychological performance, two female, disease duration-matched patients differing in initially impaired body side were followed over six months.

Results: A distinct pattern of neural atrophy and neuropsychological performance was revealed for both CBS: Patients with initial right-sided impairment (r-CBS) revealed atrophy predominantly in frontoparietal areas and showed, except from apraxia, no other cognitive deficits. In contrast, patients with impairment of the left body side (l-CBS) revealed more widespread atrophy, extending from frontoparietal to orbitofrontal and temporal regions; and apraxia, perceptional and memory deficits could be found. A similar pattern of morphological and neuropsychological differences was found for the individual disease progression in l-CBS and r-CBS single cases.

Conclusions: For similar durations of disease, volumetric grey matter loss related to CBS pathology appeared earlier and progressed faster in l-CBS than in r-CBS. Cognitive impairment in r-CBS was characterized by apraxia, and additional memory and perceptional deficits for l-CBS.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Basal Ganglia Diseases* / pathology
  • Basal Ganglia Diseases* / physiopathology
  • Basal Ganglia* / pathology
  • Basal Ganglia* / physiopathology
  • Cross-Sectional Studies
  • Female
  • Follow-Up Studies
  • Gray Matter* / pathology
  • Gray Matter* / physiopathology
  • Humans
  • Male
  • Middle Aged
  • Neurodegenerative Diseases* / pathology
  • Neurodegenerative Diseases* / physiopathology
  • Syndrome

Grants and funding

The project was supported by the “Helmholtz Alliance for Mental Health in an Ageing Society” (HelMA, HA-215) and the portfolio theme “Supercomputing and Modeling the Human brain” by the Helmholtz Association. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.