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Neurodegeneration of the Globus Pallidus Internus as a Neural Correlate to Dopa-Response in Freezing of Gait.
Lench, Daniel H; Keith, Kathryn; Wilson, Sandra; Padgett, Lucas; Benitez, Andreana; Ramakrishnan, Viswanathan; Jensen, Jens H; Bonilha, Leonardo; Revuelta, Gonzalo J.
Affiliation
  • Lench DH; Department of Neurology, Medical University of South Carlina, Charleston, SC, USA.
  • Keith K; Department of Public Health Sciences, Medical University of South Carlina, Charleston, SC, USA.
  • Wilson S; Department of Neurology, Medical University of South Carlina, Charleston, SC, USA.
  • Padgett L; Department of Neurology, Medical University of South Carlina, Charleston, SC, USA.
  • Benitez A; Department of Neurology, Medical University of South Carlina, Charleston, SC, USA.
  • Ramakrishnan V; Center for Biomedical Imaging, Medical University of South Carlina, Charleston, SC, USA.
  • Jensen JH; Department of Public Health Sciences, Medical University of South Carlina, Charleston, SC, USA.
  • Bonilha L; Department of Neuroscience, Medical University of South Carlina, Charleston, SC, USA.
  • Revuelta GJ; Center for Biomedical Imaging, Medical University of South Carlina, Charleston, SC, USA.
J Parkinsons Dis ; 12(4): 1241-1250, 2022.
Article de En | MEDLINE | ID: mdl-35367969
BACKGROUND: Background: Parkinson's disease (PD) patients who develop freezing of gait (FOG) have reduced mobility and independence. While some patients experience improvement in their FOG symptoms with dopaminergic therapies, a subset of patients have little to no response. To date, it is unknown what changes in brain structure underlie dopa-response and whether this can be measured using neuroimaging approaches. OBJECTIVE: We tested the hypothesis that structural integrity of brain regions (subthalamic nucleus and globus pallidus internus, GPi) which link basal ganglia to the mesencephalic locomotor region (MLR), a region involved in automatic gait, would be associated with FOG response to dopaminergic therapy. METHODS: In this observational study, thirty-six participants with PD and definite FOG were recruited to undergo diffusion kurtosis imaging (DKI) and multiple assessments of dopa responsiveness (UPDRS scores, gait times ON versus OFF medication). RESULTS: The right GPi in participants with dopa-unresponsive FOG showed reduced fractional anisotropy, mean kurtosis (MK), and increased radial diffusivity relative to those with dopa-responsive FOG. Furthermore, using probabilistic tractography, we observed reduced MK and increased mean diffusivity along the right GPi-MLR tract in dopa-unresponsive FOG. MK in the right GPi was associated with a subjective dopa-response for FOG (r = -0.360, df = 30, p = 0.043) but not overall motor dopa-response. CONCLUSION: These results support structural integrity of the GPi as a correlate to dopa-response in FOG. Additionally, this study suggests DKI metrics may be a sensitive biomarker for clinical studies targeting dopaminergic circuitry and improvements in FOG behavior.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Maladie de Parkinson / Troubles neurologiques de la marche Type d'étude: Etiology_studies / Observational_studies Limites: Humans Langue: En Journal: J Parkinsons Dis Année: 2022 Type de document: Article Pays d'affiliation: États-Unis d'Amérique Pays de publication: Pays-Bas

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Maladie de Parkinson / Troubles neurologiques de la marche Type d'étude: Etiology_studies / Observational_studies Limites: Humans Langue: En Journal: J Parkinsons Dis Année: 2022 Type de document: Article Pays d'affiliation: États-Unis d'Amérique Pays de publication: Pays-Bas