Evidence map›Paper›PMID 34196700›Full record

ArticleBrain : a journal of neurology2021

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

Christopher E J Doppler, Martin B Kinnerup, Corinna Brune, Ezequiel Farrher, Matthew Betts, Tatyana D Fedorova, Jeppe L Schaldemose, Karoline Knudsen, Rola Ismail, Aline D Seger and 7 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Brain : a journal of neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
8.3field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

61 citing papers in PubMed, 98 citations in OpenAlex.

  1. Trial
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  5. Vulnerability of locus coeruleus connections to aging and Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
  6. Article
  7. The Noradrenergic Brain in Parkinson's Disease.Current neurology and neuroscience reports · 2026
    Review
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1 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 3 countries.

Christopher E J DopplerInstitute of Neuroscience and Medicine (INM-3), Forschungszentrum Jülich, D-52425 Jülich, Germany.ORCID 0000-0002-1341-0389
Martin B KinnerupDepartment of Nuclear Medicine and PET, Aarhus University Hospital, DK-8200 Aarhus N, Denmark.
Corinna BruneFaculty of Medicine and University Hospital Cologne, Department of Neurology, University of Cologne, D-50937 Köln, Germany.
Ezequiel FarrherInstitute of Neuroscience and Medicine (INM-4), Forschungszentrum Jülich, D-52425 Jülich, Germany.
Matthew BettsGerman Center for Neurodegenerative Diseases (DZNE), D-39120 Magdeburg, Germany.
Tatyana D FedorovaDepartment of Nuclear Medicine and PET, Aarhus University Hospital, DK-8200 Aarhus N, Denmark.
Jeppe L SchaldemoseDepartment of Nuclear Medicine and PET, Aarhus University Hospital, DK-8200 Aarhus N, Denmark.
Karoline KnudsenDepartment of Nuclear Medicine and PET, Aarhus University Hospital, DK-8200 Aarhus N, Denmark.
Rola IsmailDepartment of Nuclear Medicine and PET, Aarhus University Hospital, DK-8200 Aarhus N, Denmark.
Aline D SegerInstitute of Neuroscience and Medicine (INM-3), Forschungszentrum Jülich, D-52425 Jülich, Germany.
Allan K HansenDepartment of Nuclear Medicine and PET, Aarhus University Hospital, DK-8200 Aarhus N, Denmark.
Kristian StærDepartment of Nuclear Medicine and PET, Aarhus University Hospital, DK-8200 Aarhus N, Denmark.
Gereon R FinkInstitute of Neuroscience and Medicine (INM-3), Forschungszentrum Jülich, D-52425 Jülich, Germany.
David J BrooksDepartment of Nuclear Medicine and PET, Aarhus University Hospital, DK-8200 Aarhus N, Denmark.ORCID 0000-0003-2602-2518
Adjmal NahimiDepartment of Nuclear Medicine and PET, Aarhus University Hospital, DK-8200 Aarhus N, Denmark.
Per BorghammerDepartment of Nuclear Medicine and PET, Aarhus University Hospital, DK-8200 Aarhus N, Denmark.ORCID 0000-0001-6391-8052
Michael SommerauerInstitute of Neuroscience and Medicine (INM-3), Forschungszentrum Jülich, D-52425 Jülich, Germany.ORCID 0000-0001-5723-9766
Aarhus University Hospital · DKForschungszentrum Jülich · DEGerman Center for Neurodegenerative Diseases · DEUniversity of Cologne · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

AgedAged, 80 and overFemaleHumansLocus CoeruleusMagnetic Resonance ImagingMaleMiddle AgedMultimodal ImagingNorepinephrine Plasma Membrane Transport ProteinsParkinson DiseasePositron-Emission TomographyNorepinephrine Plasma Membrane Transport ProteinsSLC6A2 protein, humanMeNERneuromelaninnoradrenalineParkinson’s diseasepositron emission tomography

Identifiers

PMID34196700
OpenAlexW3175286193

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.