Evidence map›Paper›PMID 35626415›Full record

ArticleDiagnostics (Basel, Switzerland)2022

Baseline Cerebrospinal Fluid α-Synuclein in Parkinson's Disease Is Associated with Disease Progression and Cognitive Decline.

Anna Emdina, Peter Hermann, Daniela Varges, Sabine Nuhn, Stefan Goebel, Timothy Bunck, Fabian Maass, Matthias Schmitz, Franc Llorens, Niels Kruse and 3 more

Open access · goldAbstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 54% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

13 authors at 4 institutions in 2 countries.

Anna EmdinaDepartment of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany.
Peter HermannDepartment of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany.
Daniela VargesDepartment of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany.
Sabine NuhnDepartment of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany.
Stefan GoebelDepartment of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany.
Timothy BunckDepartment of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany.
Fabian MaassDepartment of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany.
Matthias SchmitzDepartment of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany.ORCID 0000-0002-5502-681X
Franc LlorensDepartment of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany.ORCID 0000-0002-9756-7497
Niels KruseDepartment of Neuropathology, University Medical Centre Göttingen, 37075 Göttingen, Germany.
Paul LingorDepartment of Neurology, Klinikum Rechts der Isar, Technical University of Munich, 80333 Munich, Germany.ORCID 0000-0001-9362-7096
Brit MollenhauerDepartment of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany.
Inga ZerrDepartment of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany.ORCID 0000-0002-6722-2463
Universitätsmedizin Göttingen · DEGerman Center for Neurodegenerative Diseases · DEInstituto de Salud Carlos III · ESTUM Klinikum · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biomarkers are increasingly recognized as tools in the diagnosis and prognosis of neurodegenerative diseases. No fluid biomarker for Parkinson’s disease (PD) has been established to date, but α-synuclein, a major component of Lewy bodies in PD and dementia with Lewy bodies (DLB), has become a promising candidate. Here, we investigated CSF α-synuclein in patients with PD (n = 28), PDD (n = 8), and DLB (n = 5), applying an electrochemiluminescence immunoassay. Median values were non-significantly (p = 0.430) higher in patients with PDD and DLB (287 pg/mL) than in PD (236 pg/mL). A group of n = 36 primarily non-demented patients with PD and PDD was clinically followed for up to two years. A higher baseline α-synuclein was associated with increases in Hoehn and Yahr classifications (p = 0.019) and Beck Depression Inventory scores (p < 0.001) as well as worse performance in Trail Making Test A (p = 0.017), Trail Making Test B (p = 0.043), and the Boston Naming Test (p = 0.002) at follow-up. Surprisingly, higher levels were associated with a better performance in semantic verbal fluency tests (p = 0.046). In summary, CSF α-synuclein may be a potential prognostic marker for disease progression, affective symptoms, and executive cognitive function in PD. Larger-scaled studies have to validate these findings and the discordant results for single cognitive tests in this exploratory investigation.

Indexed as

alpha-synucleinbiomarkercerebrospinal fluiddementiadementia with Lewy bodiesParkinson’s disease

Identifiers

PMID35626415
PMCPMC9140902
OpenAlexW4280497285

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.