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SHR Neuro Krebs Kardio Lipid

Birkl, C; Carassiti, D; Hussain, F; Langkammer, C; Enzinger, C; Fazekas, F; Schmierer, K; Ropele, S.
Assessment of ferritin content in multiple sclerosis brains using temperature-induced R*2 changes.
Magn Reson Med. 2018; 79(3):1609-1615 [OPEN ACCESS]
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Autor/innen der Med Uni Graz:
Birkl Christoph
Enzinger Christian
Fazekas Franz
Langkammer Christian
Ropele Stefan

Dimensions Citations:

Plum Analytics:
Current MRI techniques cannot reliably assess iron content in white matter due to the confounding diamagnetic effect of myelin. The purpose of this study was to validate with histology a novel iron mapping technique that uses the temperature dependency of the paramagnetic susceptibility in multiple sclerosis (MS) brains, where white matter has been reported to show significant variations in iron content. We investigated post mortem brain tissue from three MS patients and one control subject. Temperature-dependent R2* relaxometry was performed between 4°C and 37°C. The resulting temperature coefficient ( TcR2*) maps were compared with immunohistochemical stains for ferritin light chain. Good agreement between TcR2* maps and ferritin staining was found by way of visual comparison and quantitative analysis. The highest iron concentrations were detected at the edge of MS lesions and in the basal ganglia. For all regions, except the subcortical U-fibers, there was a significant negative correlation between the TcR2* values and the ferritin count. This study provides further evidence that TcR2* may be a reliable measure of white matter iron content due to the elimination of myelin-induced susceptibility changes and is well suited for further research into neurological diseases with distortions of the iron homeostasis. Magn Reson Med 79:1609-1615, 2018. © 2017 International Society for Magnetic Resonance in Medicine. © 2017 International Society for Magnetic Resonance in Medicine.

Find related publications in this database (Keywords)
magnetic susceptibility
multiple sclerosis
iron mapping MRI
post mortem brain
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