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ArticleMetabolomics : Official journal of the Metabolomic Society2025

Metabolomic profiling of plasma from glioma and meningioma patients based on two complementary mass spectrometry techniques.

Adrian Godlewski, Patrycja Mojsak, Tomasz Pienkowski, Tomasz Lyson, Zenon Mariak, Joanna Reszec, Karol Kaminski, Marcin Moniuszko, Adam Kretowski, Michal Ciborowski

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Article in Metabolomics : Official journal of the Metabolomic Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

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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

2 citing papers in PubMed.

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4 · The record

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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.

Adrian GodlewskiClinical Research Centre, Medical University of Bialystok, Bialystok, 15-276, Poland.
Patrycja MojsakClinical Research Centre, Medical University of Bialystok, Bialystok, 15-276, Poland.
Tomasz PienkowskiClinical Research Centre, Medical University of Bialystok, Bialystok, 15-276, Poland.
Tomasz LysonDepartment of Neurosurgery, Medical University of Bialystok, Bialystok, 15-276, Poland.
Zenon MariakDepartment of Neurosurgery, Medical University of Bialystok, Bialystok, 15-276, Poland.
Joanna ReszecDepartment of Medical Pathomorphology, Medical University of Bialystok, Bialystok, 15-276, Poland.
Karol KaminskiDepartment of Population Medicine and Lifestyle Diseases Prevention, Medical University of Bialystok, Bialystok, 15-276, Poland.
Marcin MoniuszkoDepartment of Regenerative Medicine and Immune Regulation, Medical University of Bialystok, Bialystok, 15-276, Poland.
Adam KretowskiClinical Research Centre, Medical University of Bialystok, Bialystok, 15-276, Poland.
Michal CiborowskiClinical Research Centre, Medical University of Bialystok, Bialystok, 15-276, Poland. michal.ciborowski@umb.edu.pl.

Funding

Ministry of Education and Science Excellence Initiative-Research UniversityNational Center for Research and Development POIR.04.01.04-00-0052/18Subsidy of the Medical University of Bialystok B.SUB.23.110
6 · The paper itself

Abstract

introductionExtracranial and intracranial tumors are a diverse group of malignant and benign neoplasms, influenced by multiple factors. Given the complex nature of these tumors and usually late or accidental diagnosis, minimally invasive, rapid, early, and accurate diagnostic methods are urgently required. Metabolomics offers promising insights into central nervous system tumors by uncovering distinctive metabolic changes linked to tumor development.

objectivesThis study aimed to elucidate the role of altered metabolites and the associated biological pathways implicated in the development of gliomas and meningiomas.

methodsThe study was conducted on 95 patients with gliomas, 68 patients with meningiomas, and 71 subjects as a control group. The metabolic profiling of gliomas and meningiomas achieved by integrating untargeted metabolomic analysis based on GC-MS and targeted analysis performed using LC-MS/MS represents the first comprehensive study. Three comparisons (gliomas or meningiomas vs. controls as well as gliomas vs. meningiomas) were performed to reveal statistically significant metabolites.

resultsComparative analysis revealed 97, 56, and 27 significant metabolites for gliomas vs. controls, meningiomas vs. controls and gliomas vs. meningiomas comparison, respectively. Moreover, among above mentioned comparisons unique metabolites involved in arginine biosynthesis and metabolism, the Krebs cycle, and lysine degradation pathways were found. Notably, 2-aminoadipic acid has been identified as a metabolite that can be used in distinguishing two tumor types.

conclusionsOur results provide a deeper understanding of the metabolic changes associated with brain tumor development and progression.

Indexed as

Brain NeoplasmsGliomaMeningeal NeoplasmsMeningiomaMetabolomicsAdultAgedChromatography, LiquidFemaleGas Chromatography-Mass SpectrometryHumansMaleMetabolomeMiddle AgedTandem Mass SpectrometryBrain tumor biochemistryGliomaMeningiomaMetabolomicsTargeted and untargeted metabolomics

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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.