Evidence map›Paper›PMID 36694577›Full record

ArticleBrain communications2023

Identification of a possible proteomic biomarker in Parkinson's disease: discovery and replication in blood, brain and cerebrospinal fluid.

Laura Winchester, Imelda Barber, Michael Lawton, Jessica Ash, Benjamine Liu, Samuel Evetts, Lucinda Hopkins-Jones, Suppalak Lewis, Catherine Bresner, Ana Belen Malpartida and 9 more

Open access · goldAbstract read
In one paragraph

Article in Brain communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

23 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
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  7. Review
  8. Article
  9. Mass Spectrometry-Based Comparative Analysis ofACS chemical neuroscience · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Recent Advances in Human Cerebrospinal Fluid Proteomics.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. The complement system in neurodegenerative diseases.Clinical science (London, England : 1979) · 2024
    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

19 authors at 5 institutions in 1 country.

Laura WinchesterDepartment of Psychiatry, University of Oxford, Oxford OX3 7JX, UK.ORCID https://orcid.org/0000-0003-3826-7694
Imelda BarberDepartment of Psychiatry, University of Oxford, Oxford OX3 7JX, UK.
Michael LawtonPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Jessica AshDepartment of Psychiatry, University of Oxford, Oxford OX3 7JX, UK.
Benjamine LiuDepartment of Psychiatry, University of Oxford, Oxford OX3 7JX, UK.
Samuel EvettsOxford Parkinson's Disease Centre and Division of Neurology, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
Lucinda Hopkins-JonesDivision of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, Wales, UK.
Suppalak LewisDivision of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, Wales, UK.
Catherine BresnerDivision of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, Wales, UK.
Ana Belen MalpartidaOxford Parkinson's Disease Centre, Kavli Institute for Nanoscience Discovery, Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK.
Nigel WilliamsDivision of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, Wales, UK.ORCID https://orcid.org/0000-0003-1177-6931
Steve GentlemenDepartment of Brain Sciences, Imperial College London, London, UK.
Richard Wade-MartinsOxford Parkinson's Disease Centre, Kavli Institute for Nanoscience Discovery, Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK.
Brent RyanOxford Parkinson's Disease Centre, Kavli Institute for Nanoscience Discovery, Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK.
Alejo Holgado-NevadoDepartment of Psychiatry, University of Oxford, Oxford OX3 7JX, UK.
Michele HuOxford Parkinson's Disease Centre and Division of Neurology, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
Yoav Ben-ShlomoPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Donald GrossetInstitute of Neuroscience and Psychology, University of Glasgow, Glasgow, UK.
Simon LovestoneDepartment of Psychiatry, University of Oxford, Oxford OX3 7JX, UK.
University of Oxford · GBCardiff University · GBUniversity of Bristol · GBImperial College London · GBUniversity of Glasgow · GB

Funding

Medical Research Council MC_EX_MR/N50192X/1Medical Research Council MR/L010305/1Medical Research Council MR/L023784/2Medical Research Council MR/M024962/1Medical Research Council MR/N029453/1Medical Research Council MR/P007058/1Parkinson's UK G-0801Parkinson's UK H-1102Parkinson's UK H-1301Parkinson's UK J-0901Parkinson's UK J-1301Parkinson's UK K-1003
6 · The paper itself

Abstract

Biomarkers to aid diagnosis and delineate the progression of Parkinson's disease are vital for targeting treatment in the early phases of the disease. Here, we aim to discover a multi-protein panel representative of Parkinson's and make mechanistic inferences from protein expression profiles within the broader objective of finding novel biomarkers. We used aptamer-based technology (SomaLogic®) to measure proteins in 1599 serum samples, 85 cerebrospinal fluid samples and 37 brain tissue samples collected from two observational longitudinal cohorts (the Oxford Parkinson's Disease Centre and Tracking Parkinson's) and the Parkinson's Disease Brain Bank, respectively. Random forest machine learning was performed to discover new proteins related to disease status and generate multi-protein expression signatures with potential novel biomarkers. Differential regulation analysis and pathway analysis were performed to identify functional and mechanistic disease associations. The most consistent diagnostic classifier signature was tested across modalities [cerebrospinal fluid (area under curve) = 0.74,

Indexed as

biomarkerParkinson’s diseaseproteomics

Identifiers

PMID36694577
PMCPMC9856276
OpenAlexW4313212463

What OpenQuestion holds

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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.