Evidence map›Paper›PMID 32375873›Full record

ArticleTranslational neurodegeneration2020

CSF total and oligomeric α-Synuclein along with TNF-α as risk biomarkers for Parkinson's disease: a study in LRRK2 mutation carriers.

Nour K Majbour, Jan O Aasly, Eldbjørg Hustad, Mercy A Thomas, Nishant N Vaikath, Naser Elkum, Wilma D J van de Berg, Takahiko Tokuda, Brit Mollenhauer, Henk W Berendse and 1 more

Open access · goldAbstract read
In one paragraph

Article in Translational neurodegeneration, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
3.0field-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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 61 citations in OpenAlex.

  1. Pooled it
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  7. Article
  8. Cell-Free DNA and Mitochondria in Parkinson's Disease.International journal of molecular sciences · 2025
    Review
  9. Article
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  13. Article
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  16. Early diagnosis of Parkinson's disease: biomarker study.Frontiers in aging neuroscience · 2025
    Review
  17. Review
  18. Review
  19. Review
  20. Protein Translation in the Pathogenesis of Parkinson's Disease.International journal of molecular sciences · 2024
    Review
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

11 authors at 7 institutions in 5 countries.

Nour K MajbourNeurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Qatar Foundation, P.O. Box 5825, Doha, Qatar.
Jan O AaslyDepartment of Neuroscience, Norwegian University of Science and Technology, (NTNU), Trondheim, Norway.
Eldbjørg HustadDepartment of Neuroscience, Norwegian University of Science and Technology, (NTNU), Trondheim, Norway.
Mercy A ThomasNeurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Qatar Foundation, P.O. Box 5825, Doha, Qatar.
Nishant N VaikathNeurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Qatar Foundation, P.O. Box 5825, Doha, Qatar.
Naser ElkumClinical Epidemiology, Sidra Medical and Research Center, Doha, Qatar.
Wilma D J van de BergDepartment of Anatomy and Neurosciences, Neuroscience Campus Amsterdam, VU University Medical Centre, Amsterdam, the Netherlands.
Takahiko TokudaDepartment of Neurology, Research Institute for Geriatrics, Kyoto Prefectural University of Medicine, Kyoto, 602-0841, Japan.
Brit MollenhauerParacelsus-Elena-Klinik, Klinikstraße, Kassel, and University Medical Center Göttingen, Department of Neurology, Göttingen, Germany.
Henk W BerendseDepartment of Neurology, Amsterdam UMC, location VU University Medical Centre, Amsterdam, The Netherlands.
Omar M A El-AgnafNeurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Qatar Foundation, P.O. Box 5825, Doha, Qatar. oelagnaf@qf.org.qa.
Qatar Foundation · QASt Olav's University Hospital · NOAmsterdam Neuroscience · NLAmsterdam UMC Location VUmc · NLKyoto Prefectural University of Medicine · JPSidra Medical and Research Center · QAUniversitätsmedizin Göttingen · DE

Funding

Qatar National Research Fund (NPRP No.: 8-517-3-112
6 · The paper itself

Abstract

backgroundAsymptomatic carriers of leucine-rich repeat kinase 2 (LRRK2) gene mutations constitute an ideal population for discovering prodromal biomarkers of Parkinson's disease (PD). In this study, we aim to identify CSF candidate risk biomarkers of PD in individuals with LRRK2 mutation carriers.

methodsWe measured the levels of CSF total- (t-), oligomeric (o-) and phosphorylated S129 (pS129-) α-syn, total-tau (tTau), phosphorylated threonine 181 tau (pTau), amyloid-beta 40 (Aβ-40), amyloid-beta-42 (Aβ-42) and 40 inflammatory chemokines in symptomatic (n = 23) and asymptomatic (n = 51) LRRK2 mutation carriers, subjects with a clinical diagnosis of PD (n = 60) and age-matched healthy controls (n = 34). General linear models corrected for age and gender were performed to assess differences in CSF biomarkers between the groups. Markers that varied significantly between the groups were then analyzed using backward-elimination logistic regression analysis to identify an ideal biomarkers panel of prodromal PD.

resultsDiscriminant function analysis revealed low levels of CSF t-α-syn, high levels of CSF o-α-syn and TNF-α best discriminated asymptomatic LRRK2 mutation carriers from both symptomatic PD and healthy controls. Assessing the discriminative power using receiver operating curve analysis, an area under the curve > 0.80 was generated.

conclusionsThe current study suggests that CSF t-, o-α-syn and TNF-α are candidate risk biomarkers for the detection of PD at the prodromal stage. Our findings also highlight the dynamic interrelationships between CSF proteins and the importance of using a biomarkers' panel approach for an accurate and timely diagnosis of PD.

Indexed as

HeterozygoteAdultAgedalpha-SynucleinBiomarkersCohort StudiesFemaleGenetic Predisposition to DiseaseHumansLeucine-Rich Repeat Serine-Threonine Protein Kinase-2MaleMiddle AgedMutationParkinson DiseaseProdromal SymptomsTumor Necrosis Factor-alphaalpha-SynucleinBiomarkersLeucine-Rich Repeat Serine-Threonine Protein Kinase-2LRRK2 protein, humanTumor Necrosis Factor-alphaAlpha-synuclein oligomersBiomarkersInflammatory markersLRRK2 mutation carriersParkinson’s disease

Identifiers

PMID32375873
PMCPMC7201744
OpenAlexW3022979459

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.