Hemispheric Network Expression in Parkinson’s Disease: Relationship to Dopaminergic Asymmetries
Journal of Parkinson s Disease, vol. 10, pp. 1737–1749
Abstract
BACKGROUND: Parkinson's disease (PD) is characterized by brain metabolic networks, specifically associated with motor and cognitive manifestations. Few studies have investigated network changes in cerebral hemispheres ipsilateral and contralateral to the clinically more affected body side. OBJECTIVE: We examined hemispheric network abnormalities and their relationship to striatal dopaminergic deficits in PD patients at different stages. METHODS: 45 PD patients underwent dual-tracer positron emission tomography (PET) with 18F-fluorodeoxyglucose (FDG) and 18F-fluorodopa (FDOPA) in a high-resolution PET scanner. In all patients, we computed expression levels for the PD-related motor/cognition metabolic patterns (PDRP/PDCP) as well as putamen/caudate FDOPA uptake values in both hemispheres. Resulting hemispheric measures in the PD group were compared with corresponding healthy control values and assessed across disease stages. RESULTS: Hemispheric PDRP and PDCP expression was significantly elevated contralateral and ipsilateral to the more affected body side in patients with unilateral symptoms (H&Y 1: p < 0.01) and in patients with bilateral limb involvement (H&Y 2-3: p < 0.001; H&Y 4: p < 0.003). Elevations in pattern expression were symmetrical at all disease stages. By contrast, FDOPA uptake in the caudate and putamen was reduced bilaterally (p < 0.002), with lower values on both sides at more advanced disease stages. Hemispheric uptake was asymmetrical in both striatal regions, with lower contralateral values at all disease stages. The magnitude of hemispheric uptake asymmetry was smaller with more advanced disease, reflecting greater change ipsilaterally. CONCLUSION: Symmetrical network expression in PD represents bilateral functional effects unrelated to nigrostriatal dopaminergic asymmetries.
Authors 9
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Feinstein Institute for Medical Research
Affiliation as printed
Center for Neurosciences, The Feinstein Institutes for Medical Research, Manhasset, NY, USA
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Florian Holtbernd Aachen JARA Brain Institute Molecular Neuroscience and Neuroimaging (INM-11) Department of Neurology
Forschungszentrum Jülich · Jülich Aachen Research Alliance · RWTH Aachen University
Affiliation as printed
Institute of Neuroscience and Medicine 4 (INM-4), Juelich Research Centre, Juelich, Germany
JARA-BRAIN Institute Molecular Neuroscience and Neuroimaging, Juelich Research Centre and RWTH Aachen University, Aachen, Germany
RWTH Aachen University, Department of Neurology, Aachen, Germany
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Feinstein Institute for Medical Research
Affiliation as printed
Center for Neurosciences, The Feinstein Institutes for Medical Research, Manhasset, NY, USA
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Feinstein Institute for Medical Research
Affiliation as printed
Center for Neurosciences, The Feinstein Institutes for Medical Research, Manhasset, NY, USA
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Feinstein Institute for Medical Research
Affiliation as printed
Center for Neurosciences, The Feinstein Institutes for Medical Research, Manhasset, NY, USA
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Forschungszentrum Jülich · University of Cologne
Affiliation as printed
Cognitive Neuroscience, Institute of Neuroscience and Medicine (INM-3), Jülich Research Centre, Jülich, Germany
Department of Neurology, University of Cologne, Cologne, Germany
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Forschungszentrum Jülich · Universitätsklinikum Gießen und Marburg
Affiliation as printed
Cognitive Neuroscience, Institute of Neuroscience and Medicine (INM-3), Jülich Research Centre, Jülich, Germany
Department of Neurology, University Hospital of Giessen and Marburg, Marburg, Germany
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Universitätsklinikum Gießen und Marburg
Affiliation as printed
Center for Mind, Brain and Behavior, Universities Marburg and Giessen, Marburg, Germany
Department of Neurology, University Hospital of Giessen and Marburg, Marburg, Germany
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David Eidelberg corresponding
Feinstein Institute for Medical Research
Affiliation as printed
Center for Neurosciences, The Feinstein Institutes for Medical Research, Manhasset, NY, USA
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