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Is R(2)* a New MRI Biomarker for the Progression of Parkinson’s Disease? A Longitudinal Follow-Up

PURPOSE: To study changes of iron content in basal ganglia in Parkinson’s disease (PD) through a three-year longitudinal follow-up of the effective transverse relaxation rate R(2)*, a validated MRI marker of brain iron content which can be rapidly measured under clinical conditions. METHODS: Twenty-...

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Detalles Bibliográficos
Autores principales: Ulla, Miguel, Bonny, Jean Marie, Ouchchane, Lemlih, Rieu, Isabelle, Claise, Beatrice, Durif, Franck
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585727/
https://www.ncbi.nlm.nih.gov/pubmed/23469252
http://dx.doi.org/10.1371/journal.pone.0057904
Descripción
Sumario:PURPOSE: To study changes of iron content in basal ganglia in Parkinson’s disease (PD) through a three-year longitudinal follow-up of the effective transverse relaxation rate R(2)*, a validated MRI marker of brain iron content which can be rapidly measured under clinical conditions. METHODS: Twenty-seven PD patients and 26 controls were investigated by a first MRI (t(0)). Longitudinal analysis was conducted among the 18 controls and 14 PD patients who underwent a second MRI (t(1)) 3 years after. The imaging protocol consisted in 6 gradient echo images obtained at different echo-times for mapping R(2)*. Quantitative exploration of basal ganglia was performed by measuring the variation of R(2)* [R(2)*(t(1)) – R(2)*(t(0))] in several regions of interest. RESULTS: During the three-year evolution of PD, R(2)* increased in Substantia nigra (SN) (by 10.2% in pars compacta, p = 0.001, and 8.1% in pars reticulata, p = 0.013) and in the caudal putamen (11.4%, p = 0.011), without significant change in controls. Furthermore, we showed a positive correlation between the variation of R(2)* and the worsening of motor symptoms of PD (p = 0.028). CONCLUSION: Significant variation of R(2)* was longitudinally observed in the SN and caudal putamen of patients with PD evolving over a three-year period, emphasizing its interest as a biomarker of disease progression. Our results suggest that R(2)* MRI follow-up could be an interesting tool for individual assessment of neurodegeneration due to PD, and also be useful for testing the efficiency of disease-modifying treatments.