Synaptic Density and Glucose Consumption in Patients with Lewy Body Diseases: An [11C]UCB‐J and [18F]FDG PET Study

Author:

Andersen Katrine B.1ORCID,Hansen Allan K.2,Schacht Anna Christina1,Horsager Jacob1ORCID,Gottrup Hanne3,Klit Henriette3,Danielsen Erik H.3,Poston Kathleen L.4ORCID,Pavese Nicola15,Brooks David J.156,Borghammer Per1ORCID

Affiliation:

1. Department of Nuclear Medicine and PET Aarhus University Hospital Aarhus Denmark

2. Department of Nuclear Medicine Aalborg University Hospital Aalborg Denmark

3. Department of Neurology Aarhus University Hospital Aarhus Denmark

4. Department of Neurology Stanford University Stanford California USA

5. Translational and Clinical Research Institute Newcastle University Newcastle upon Tyne UK

6. Department of Brain Sciences Imperial College London London UK

Abstract

AbstractBackgroundPatients with Lewy body diseases exhibit variable degrees of cortical and subcortical hypometabolism. However, the underlying causes behind this progressive hypometabolism remain unresolved. Generalized synaptic degeneration may be one key contributor.ObjectiveThe objective of this study was to investigate whether local cortical synaptic loss is proportionally linked to the magnitude of hypometabolism in Lewy body disease.MethodUsing in vivo positron emission tomography (PET) we investigated cerebral glucose metabolism and quantified the density of cerebral synapses, as measured with [18F]fluorodeoxyglucose ([18F]FDG) PET and [11C]UCB‐J, respectively. Volumes‐of‐interest were defined on magnetic resonance T1 scans and regional standard uptake value ratios‐1 values were obtained for 14 pre‐selected brain regions. Between‐group comparisons were conducted at voxel‐level.ResultsWe observed regional differences in both synaptic density and cerebral glucose consumption in our cohorts of non‐demented and demented patients with Parkinson's disease or dementia with Lewy bodies compared to healthy subjects. Additionally, voxel‐wise comparisons showed a clear difference in cortical regions between demented patients and controls for both tracers. Importantly, our findings strongly suggested that the magnitude of reduced glucose uptake exceeded the magnitude of reduced cortical synaptic density.ConclusionHere, we investigated the relationship between in vivo glucose uptake and the magnitude of synaptic density as measured using [18F]FDG PET and [11C]UCB‐J PET in Lewy body patients. The magnitude of reduced [18F]FDG uptake was greater than the corresponding decline in [11C]UCB‐J binding. Therefore, the progressive hypometabolism seen in Lewy body disorders cannot be fully explained by generalized synaptic degeneration. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Funder

Lundbeckfonden

Michael J. Fox Foundation

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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