Iron deposition in multiple sclerosis: overall load or distribution alteration?

Background Though abnormal iron deposition has been reported in specific brain regions in multiple sclerosis (MS), no data exist about whether the overall quantity of iron in the brain is altered or not. We aimed to determine whether the noted aberrant iron deposition in MS brains was a problem of o...

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Veröffentlicht in:European Radiology Experimental 2022-09, Vol.6 (1), p.49-49, Article 49
Hauptverfasser: Hamdy, Eman, Galeel, Aya Abdel, Ramadan, Ismail, Gaber, Dina, Mustafa, Haytham, Mekky, Jaidaa
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Sprache:eng
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Zusammenfassung:Background Though abnormal iron deposition has been reported in specific brain regions in multiple sclerosis (MS), no data exist about whether the overall quantity of iron in the brain is altered or not. We aimed to determine whether the noted aberrant iron deposition in MS brains was a problem of overall load or regional distribution in a cohort of MS patients. Methods An experienced neuroradiologist, a radiology software engineer, and four neurologists analysed data from quantitative susceptibility maps reconstructed from 3-T magnetic resonance brain images of 30 MS patients and 15 age- and sex-matched healthy controls. Global brain iron load was calculated, and the regional iron concentrations were assessed in 1,000 regions of interest placed in MS lesions in different locations, normal appearing white matter, thalami, and basal ganglia. Results Global brain iron load was comparable between patients and controls after adjustment for volume ( p = 0.660), whereas the regional iron concentrations were significantly different in patients than in control ( p ≤ 0.031). There was no significant correlation between global iron load and clinical parameters, whereas regional iron concentrations correlated with patients’ age, disease duration, and disability grade ( p ≤ 0.039). Conclusions The aberrant iron deposition noted in MS seems to be a problem of regional distribution rather than an altered global brain iron load.
ISSN:2509-9280
2509-9280
DOI:10.1186/s41747-022-00279-9