Journal
MOVEMENT DISORDERS
Volume 37, Issue 9, Pages 1948-1952Publisher
WILEY
DOI: 10.1002/mds.29145
Keywords
neuroferritinopathy; iron chelation; neuroprotection; Parkinson's disease; spinocerebellar ataxia
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This study assessed the efficacy of conservative iron chelation with deferiprone in patients with neuroferritinopathy. The results showed that deferiprone treatment led to improvement in patients' conditions, and early initiation of treatment was associated with better outcomes. This study suggests that conservative iron chelation should be further examined as a potential treatment for neuroferritinopathy.
Background Neuroferritinopathy is a rare inherited neurodegenerative disease with brain iron accumulation characterized by brain iron overload resulting in progressive movement disorders. No treatment is currently available. Objective We assessed conservative iron chelation with deferiprone at 30 mg/kg/day on the disease progression with controlled periods of discontinuation. Methods Four patients with confirmed molecular diagnosis of neuroferritinopathy were given deferiprone at different stages of disease progression and with clinical and biological monitoring to control benefit and risk. Results The four patients showed slight to high improvement. In one case, we managed to stabilize disease progression for more than 11 years. In another case, we were able to reverse symptoms after a few months of treatment. The earliest the treatment was started, the most efficient it was on disease progression. Conclusions Conservative iron chelation should be further assessed in neuroferritinopathy. (c) 2022 International Parkinson and Movement Disorder Society.
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