Regional locus coeruleus degeneration is uncoupled from noradrenergic terminal loss in Parkinson’s disease

Author:

Doppler Christopher E J12ORCID,Kinnerup Martin B3,Brune Corinna2,Farrher Ezequiel4,Betts Matthew567,Fedorova Tatyana D3,Schaldemose Jeppe L3,Knudsen Karoline3,Ismail Rola3,Seger Aline D12,Hansen Allan K3,Stær Kristian3,Fink Gereon R12,Brooks David J389ORCID,Nahimi Adjmal3,Borghammer Per3ORCID,Sommerauer Michael123ORCID

Affiliation:

1. Institute of Neuroscience and Medicine (INM-3), Forschungszentrum Jülich, D-52425 Jülich, Germany

2. Faculty of Medicine and University Hospital Cologne, Department of Neurology, University of Cologne, D-50937 Köln, Germany

3. Department of Nuclear Medicine and PET, Aarhus University Hospital, DK-8200 Aarhus N, Denmark

4. Institute of Neuroscience and Medicine (INM-4), Forschungszentrum Jülich, D-52425 Jülich, Germany

5. German Center for Neurodegenerative Diseases (DZNE), D-39120 Magdeburg, Germany

6. Institute of Cognitive Neurology and Dementia Research, Otto-von-Guericke-University Magdeburg, D-39120 Magdeburg, Germany

7. Center for Behavioral Brain Sciences, University of Magdeburg, D-39120 Magdeburg, Germany

8. Division of Brain Sciences, Imperial College London, London SW7 2AZ, UK

9. Institute of Translational and Clinical Research, University of Newcastle upon Tyne, Newcastle upon Tyne NE1 7RU, UK

Abstract

Abstract Previous studies have reported substantial involvement of the noradrenergic system in Parkinson’s disease. Neuromelanin-sensitive MRI sequences and PET tracers have become available to visualize the cell bodies in the locus coeruleus and the density of noradrenergic terminal transporters. Combining these methods, we investigated the relationship of neurodegeneration in these distinct compartments in Parkinson’s disease. We examined 93 subjects (40 healthy controls and 53 Parkinson’s disease patients) with neuromelanin-sensitive turbo spin-echo MRI and calculated locus coeruleus-to-pons signal contrasts. Voxels with the highest intensities were extracted from published locus coeruleus coordinates transformed to individual MRI. To also investigate a potential spatial pattern of locus coeruleus degeneration, we extracted the highest signal intensities from the rostral, middle, and caudal third of the locus coeruleus. Additionally, a study-specific probabilistic map of the locus coeruleus was created and used to extract mean MRI contrast from the entire locus coeruleus and each rostro-caudal subdivision. Locus coeruleus volumes were measured using manual segmentations. A subset of 73 subjects had 11C-MeNER PET to determine noradrenaline transporter density, and distribution volume ratios of noradrenaline transporter-rich regions were computed. Patients with Parkinson’s disease showed reduced locus coeruleus MRI contrast independently of the selected method (voxel approaches: P < 0.0001, P < 0.001; probabilistic map: P < 0.05), specifically on the clinically-defined most affected side (P < 0.05), and reduced locus coeruleus volume (P < 0.0001). Reduced MRI contrast was confined to the middle and caudal locus coeruleus (voxel approach, rostral: P = 0.48, middle: P < 0.0001, and caudal: P < 0.05; probabilistic map, rostral: P = 0.90, middle: P < 0.01, and caudal: P < 0.05). The noradrenaline transporter density was lower in patients with Parkinson’s diseasein all examined regions (group effect P < 0.0001). No significant correlation was observed between locus coeruleus MRI contrast and noradrenaline transporter density. In contrast, the individual ratios of noradrenaline transporter density and locus coeruleus MRI contrast were lower in Parkinson’s disease patients in all examined regions (group effect P < 0.001). Our multimodal imaging approach revealed pronounced noradrenergic terminal loss relative to cellular locus coeruleus degeneration in Parkinson’s disease; the latter followed a distinct spatial pattern with the middle-caudal portion being more affected than the rostral part. The data shed first light on the interaction between the axonal and cell body compartments and their differential susceptibility to neurodegeneration in Parkinson’s disease, which may eventually direct research towards potential novel treatment approaches.

Funder

Deutsche Forschungsgemeinschaft

German Research Foundation

Clinical Medicine Programme

Olav Thon Foundation

Danish Association of Parkinson’s Disease

Swiss National Science Foundation

Hildegard Henssler-Stiftung

Koeln Fortune Program/Faculty of Medicine, University of Cologne

Else Kröner-Fresenius-Stiftung

Lundbeck foundation

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

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