Evidence map›Paper›PMID 33332647›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2021

Soluble CD163 Changes Indicate Monocyte Association With Cognitive Deficits in Parkinson's Disease.

Sara Konstantin Nissen, Sara Almeida Ferreira, Marlene Christina Nielsen, Claudia Schulte, Kalpana Shrivastava, Dorle Hennig, Anders Etzerodt, Jonas Heilskov Graversen, Daniela Berg, Walter Maetzler and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 2 pooled it
3.4field-weighted citation impact, top 7% 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

32 citing papers in PubMed, 2 syntheses or guidelines pooled it, 56 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. What's in a name? reframing advanced Parkinson's disease as a multidimensional state.Journal of neural transmission (Vienna, Austria : 1996) · 2026
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Investigating the Relationship of Serum CD163, YKL40 and VILIP-1 Levels with Autism Severity and Language-cognitive Development in Preschool Children with Autism.Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology · 2024
    Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 6 institutions in 3 countries.

Sara Konstantin NissenDANDRITE and Department of Biomedicine, Aarhus University, Aarhus, Denmark.ORCID 0000-0003-4711-0875
Sara Almeida FerreiraDANDRITE and Department of Biomedicine, Aarhus University, Aarhus, Denmark.
Marlene Christina NielsenDepartment of Clinical Biochemistry, Aarhus University Hospital, Aarhus, Denmark.
Claudia SchulteCenter of Neurology, Department of Neurodegeneration and Hertie-Institute for Clinical Brain Research & German Center for Neurodegenerative Diseases, University of Tuebingen, Tuebingen, Germany.ORCID 0000-0003-4006-1265
Kalpana ShrivastavaDANDRITE and Department of Biomedicine, Aarhus University, Aarhus, Denmark.
Dorle HennigDepartment of Molecular Medicine, University of Southern Denmark, Odense, Denmark.
Anders EtzerodtDANDRITE and Department of Biomedicine, Aarhus University, Aarhus, Denmark.
Jonas Heilskov GraversenDepartment of Molecular Medicine, University of Southern Denmark, Odense, Denmark.
Daniela BergCenter of Neurology, Department of Neurodegeneration and Hertie-Institute for Clinical Brain Research & German Center for Neurodegenerative Diseases, University of Tuebingen, Tuebingen, Germany.
Walter MaetzlerDepartment of Neurology, Christian-Albrechts University, Kiel, Germany.
Anne PanhelainenInstitute of Biotechnology, University of Helsinki, Helsinki, Finland.
Holger Jon MøllerDepartment of Clinical Biochemistry, Aarhus University Hospital, Aarhus, Denmark.
Kathrin BrockmannCenter of Neurology, Department of Neurodegeneration and Hertie-Institute for Clinical Brain Research & German Center for Neurodegenerative Diseases, University of Tuebingen, Tuebingen, Germany.
Marina Romero-RamosDANDRITE and Department of Biomedicine, Aarhus University, Aarhus, Denmark.ORCID 0000-0003-0970-578X
Aarhus University · DKGerman Center for Neurodegenerative Diseases · DEAarhus University Hospital · DKUniversity of Southern Denmark · DKChristian-Albrechts-Universität zu Kiel · DEUniversity of Helsinki · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundParkinson's disease (PD) is a neurodegenerative disorder with a significant immune component, as demonstrated by changes in immune biomarkers in patients' biofluids. However, which specific cells are responsible for those changes is unclear because most immune biomarkers can be produced by various cell types.

objectivesThe aim of this study was to explore monocyte involvement in PD.

methodsWe investigated the monocyte-specific biomarker sCD163, the soluble form of the receptor CD163, in cerebrospinal fluid (CSF) and serum in two experiments, and compared it with other biomarkers and clinical data. Potential connections between CD163 and alpha-synuclein were studied in vitro.

resultsCSF-sCD163 increased in late-stage PD and correlated with the PD biomarkers alpha-synuclein, Tau, and phosphorylated Tau, whereas it inversely correlated with the patients' cognitive scores, supporting monocyte involvement in neurodegeneration and cognition in PD. Serum-sCD163 increased only in female patients, suggesting a sex-distinctive monocyte response. CSF-sCD163 also correlated with molecules associated with adaptive and innate immune system activation and with immune cell recruitment to the brain. Serum-sCD163 correlated with proinflammatory cytokines and acute-phase proteins, suggesting a relation to chronic systemic inflammation. Our in vitro study showed that alpha-synuclein activates macrophages and induces shedding of sCD163, which in turn enhances alpha-synuclein uptake by myeloid cells, potentially participating in its clearance.

conclusionsOur data present sCD163 as a potential cognition-related biomarker in PD and suggest a role for monocytes in both peripheral and brain immune responses. This may be directly related to alpha-synuclein's proinflammatory capacity but could also have consequences for alpha-synuclein processing. © 2020 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Indexed as

Antigens, CDAntigens, Differentiation, MyelomonocyticCognitionParkinson DiseaseReceptors, Cell Surfacealpha-SynucleinAmyloid beta-PeptidesBiomarkersCD163 AntigenFemaleHumansMonocytesPeptide Fragmentsalpha-SynucleinAmyloid beta-PeptidesAntigens, CDAntigens, Differentiation, MyelomonocyticBiomarkersCD163 AntigenPeptide FragmentsReceptors, Cell Surfacealpha-synucleinbiomarkerscognitionmonocytessCD163

Identifiers

PMID33332647
PMCPMC8247308
OpenAlexW3114434465

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.