Hippocampal atrophy as a surrogate of neuronal involvement in Fabry disease

Andreas Fellgiebel1, Dominik O Wolf, Edwin Kolodny

  • 1Department of Psychiatry and Psychotherapy, University Medical Center Mainz, Untere Zahlbacher Str. 8, 55131, Mainz, Germany. fellgiebel@psychiatrie.klinik.uni-mainz.de

Insights

Fabry disease (FD) is linked to reduced hippocampus size, particularly in men, despite preserved memory function in affected individuals. Further research is needed to understand the progression of this brain degeneration.

Area of Science:

  • Neurology
  • Neuroimaging
  • Genetics

Background:

  • Fabry disease (FD) is characterized by cerebral micro- and macro-vasculopathy.
  • Neuronal globotriaosylceramide accumulation in the brain, including the hippocampus, is known from autopsy studies in FD.
  • Clinical relevance and imaging surrogates of hippocampal changes in FD remain under-investigated.

Purpose of the Study:

  • To investigate hippocampal volumes in clinically affected FD patients.
  • To correlate hippocampal volumes with cognitive performance, specifically memory function.
  • To explore the relationship between hippocampal atrophy, white matter lesions, and brain tissue volumes in FD.

Main Methods:

  • Manual determination of hippocampal volumes on T1-weighted MR images from 25 FD patients and 20 age-matched controls.
  • Brain segmentation analysis to measure individual white matter (WM) and gray matter (GM) volumes.
  • Statistical analysis controlling for age, white matter lesion (WML) volume, and WM/GM volumes.

Main Results:

  • Significantly decreased hippocampal volumes were observed in FD patients compared to controls, more pronounced in men.
  • No significant differences in WM and GM volumes or memory function were found between groups.
  • Hippocampal volume reduction in FD was independent of WMLs and other brain tissue atrophy, suggesting neuronal involvement.

Conclusions:

  • Hippocampal atrophy occurs in FD, likely due to neuronal globotriaosylceramide accumulation.
  • Despite hippocampal degeneration, memory function remains compensated in this young to middle-aged FD cohort.
  • Longitudinal studies are required to ascertain the progression of hippocampal degeneration and its impact on cognitive decline in FD.