Brain iron accumulation in Wilson disease: a post mortem 7 Tesla MRI - histopathological study
Language English Country England, Great Britain Media print-electronic
Document type Journal Article
PubMed
27543917
DOI
10.1111/nan.12341
Knihovny.cz E-resources
- Keywords
- Wilson disease, brain, iron accumulation, pathology, post mortem 7T MRI,
- MeSH
- Astrocytes MeSH
- Basal Ganglia diagnostic imaging metabolism pathology MeSH
- Corpus Striatum metabolism pathology MeSH
- Adult MeSH
- Hepatolenticular Degeneration diagnostic imaging metabolism pathology MeSH
- Middle Aged MeSH
- Humans MeSH
- Magnetic Resonance Imaging MeSH
- Macrophages MeSH
- Copper metabolism MeSH
- Young Adult MeSH
- Iron metabolism MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Copper MeSH
- Iron MeSH
AIMS: In Wilson disease (WD), T2/T2*-weighted (T2*w) MRI frequently shows hypointensity in the basal ganglia that is suggestive of paramagnetic deposits. It is currently unknown whether this hypointensity is related to copper or iron deposition. We examined the neuropathological correlates of this MRI pattern, particularly in relation to iron and copper concentrations. METHODS: Brain slices from nine WD and six control cases were investigated using a 7T-MRI system. High-resolution T2*w images were acquired and R2* parametric maps were reconstructed using a multigradient recalled echo sequence. R2* was measured in the globus pallidus (GP) and the putamen. Corresponding histopathological sections containing the lentiform nucleus were examined using Turnbull iron staining, and double staining combining Turnbull with immunohistochemistry for macrophages or astrocytes. Quantitative densitometry of the iron staining as well as copper and iron concentrations were measured in the GP and putamen and correlated with R2* values. RESULTS: T2*w hypointensity in the GP and/or putamen was apparent in WD cases and R2* values correlated with quantitative densitometry of iron staining. In WD, iron and copper concentrations were increased in the putamen compared to controls. R2* was correlated with the iron concentration in the GP and putamen, whereas no correlation was observed for the copper concentration. Patients with more pronounced pathological severity in the putamen displayed increased iron concentration, which correlated with an elevated number of iron-containing macrophages. CONCLUSIONS: T2/T2*w hypointensity observed in vivo in the basal ganglia of WD patients is related to iron rather than copper deposits.
2nd Department of Neurology Institute Psychiatry and Neurology Warsaw Poland
Department of Experimental and Clinical Pharmacology Medical University Warsaw Poland
Department of Neurology Ludwig Maximilians University Munich Germany
Experimental and Clinical Research Center Berlin Germany
Faculty of Chemistry Biological and Chemical Research Centre University of Warsaw Warsaw Poland
Institute of Neuropathology University Medical Center Göttingen Göttingen Germany
Institute of Neuroradiology University Medical Center Göttingen Göttingen Germany
References provided by Crossref.org
Brain morphometry in hepatic Wilson disease patients
Cerebral Iron Deposition in Neurodegeneration
Neurologic impairment in Wilson disease