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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.
Abstract:
Cerebral micro- and macro-vasculopathy have been described in Fabry disease (FD). Neuronal globotriaosylceramide accumulation in selective cortical and brain stem areas including the hippocampus has been reported by autopsy studies in FD, but clinical surrogates as well as the clinical relevance of these findings have not been investigated so far. We measured the hippocampus volumes in a group of clinically affected patients with FD and correlated the findings with the cognitive performance of the patients. Hippocampal volumes were determined manually on T1-weighted MR-images of 25 FD patients (age 36.5 ± 11.0 years) and 20 age-matched controls. Additionally, individual white matter (WM) and gray matter (GM) volumes were measured using brain segmentation analyses. After controlling for age, white matter lesion (WML) volume, and WM/GM-volumes hippocampal volumes were significantly decreased in FD. These findings were substantially more pronounced in a subgroup of men with FD. WM and WM/GM volumes, and memory function did not significantly differ between patients and controls. In patients with FD hippocampal volumes were neither significantly correlated to WML volume nor to WM or WM/GM volumes. Hippocampus atrophy was not driven by the WML or other brain tissue atrophy and seems to correlate with the neuronal involvement in FD. In this young to middle-aged Fabry cohort the hippocampus degeneration was functionally compensated without memory impairment. Longitudinal studies are needed to determine whether this degenerative component in FD will progress and, in concert with the individual WML-load, predict subsequent cognitive decline.
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