Evidence map›Paper›PMID 34577635›Full record

ArticlePharmaceuticals (Basel, Switzerland)2021

The Metabolomic Approach Reveals the Alteration in Human Serum and Cerebrospinal Fluid Composition in Parkinson's Disease Patients.

Szymon Plewa, Karolina Poplawska-Domaszewicz, Jolanta Florczak-Wyspianska, Agnieszka Klupczynska-Gabryszak, Bartosz Sokol, Wojciech Miltyk, Roman Jankowski, Wojciech Kozubski, Zenon J Kokot, Jan Matysiak

Abstract read
In one paragraph

Article in Pharmaceuticals (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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, 1 synthesis or guideline pooled it.

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  5. Association of Childhood Asthma with the Concept of Exposomics: A Short Review.Medical science monitor : international medical journal of experimental and clinical research · 2025
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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

10 authors.

Szymon PlewaDepartment of Inorganic and Analytical Chemistry, Poznan University of Medical Sciences, 60-780 Poznan, Poland.ORCID 0000-0002-9600-3980
Karolina Poplawska-DomaszewiczDepartment of Neurology, Poznan University of Medical Sciences, 60-355 Poznan, Poland.
Jolanta Florczak-WyspianskaDepartment of Neurology, Poznan University of Medical Sciences, 60-355 Poznan, Poland.
Agnieszka Klupczynska-GabryszakDepartment of Inorganic and Analytical Chemistry, Poznan University of Medical Sciences, 60-780 Poznan, Poland.ORCID 0000-0002-5028-1408
Bartosz SokolDepartment of Neurosurgery, Poznan University of Medical Sciences, 60-355 Poznan, Poland.ORCID 0000-0003-4814-2000
Wojciech MiltykDepartment of Analysis and Bioanalysis of Medicines, Medical University of Bialystok, 15-089 Bialystok, Poland.ORCID 0000-0001-5150-6093
Roman JankowskiDepartment of Neurosurgery, Poznan University of Medical Sciences, 60-355 Poznan, Poland.
Wojciech KozubskiDepartment of Neurology, Poznan University of Medical Sciences, 60-355 Poznan, Poland.
Zenon J KokotFaculty of Health Sciences, Calisia University, 62-800 Kalisz, Poland.
Jan MatysiakDepartment of Inorganic and Analytical Chemistry, Poznan University of Medical Sciences, 60-780 Poznan, Poland.ORCID 0000-0002-9993-1504

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's disease (PD) is a major public health problem. Since currently there are no reliable diagnostic tools to reveal the early steps of PD, new methods should be developed, including those searching the variations in human metabolome. Alterations in human metabolites could help to establish an earlier and more accurate diagnosis. The presented research shows a targeted metabolomics study of both of the serum and CSF from PD patients, atypical parkinsonian disorders (APDs) patients, and the control. The use of the LC-MS/MS system enabled to quantitate 144 analytes in the serum and 51 in the CSF. This information about the concentration enabled for selection of the metabolites useful for differentiation between the studied group of patients, which should be further evaluated as candidates for markers of screening and differential diagnosis of PD and APDs. Among them, the four compounds observed to be altered in both the serum and CSF seem to be the most important: tyrosine, putrescine, trans-4-hydroxyproline, and total dimethylarginine. Furthermore, we indicated the metabolic pathways potentially related to neurodegeneration processes. Our studies present evidence that the proline metabolism might be related to neurodegeneration processes underlying PD and APDs. Further studies on the proposed metabolites and founded metabolic pathways may significantly contribute to understanding the molecular background of PD and improving the diagnostics and treatment in the future.

Indexed as

amino acidscerebrospinal fluid (CSF)lipidomicsliquid chromatography–tandem mass spectrometry (LC-MS/MS)Parkinson’s diseasetargeted metabolomics

Identifiers

PMID34577635
PMCPMC8465898

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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.