Evidence map›Paper›PMID 36584284›Full record

ArticleACS chemical neuroscience2023

Artificial Neural Networks Coupled with MALDI-TOF MS Serum Fingerprinting To Classify and Diagnose Pathological Pain Subtypes in Preclinical Models.

Meritxell Deulofeu, Eladia M Peña-Méndez, Petr Vaňhara, Josef Havel, Lukáš Moráň, Lukáš Pečinka, Anna Bagó-Mas, Enrique Verdú, Victoria Salvadó, Pere Boadas-Vaello

Abstract read
In one paragraph

Article in ACS chemical neuroscience, 2023. 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
–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

1 citing paper in PubMed.

  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

10 authors.

Meritxell DeulofeuResearch Group of Clinical Anatomy, Embryology and Neuroscience (NEOMA), Department of Medical Sciences, University of Girona, Girona, Catalonia 17003, Spain.
Eladia M Peña-MéndezDepartment of Chemistry, Analytical Chemistry Division, Faculty of Sciences, University of La Laguna, 38204 San Cristóbal de La Laguna, Tenerife, Spain.ORCID 0000-0002-1474-3134
Petr VaňharaDepartment of Histology and Embryology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic.ORCID 0000-0002-7470-177X
Josef HavelDepartment of Chemistry, Faculty of Science, Masaryk University, Kamenice 5/A14, 625 00 Brno, Czech Republic.ORCID 0000-0002-6675-5671
Lukáš MoráňDepartment of Histology and Embryology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic.
Lukáš PečinkaDepartment of Chemistry, Faculty of Science, Masaryk University, Kamenice 5/A14, 625 00 Brno, Czech Republic.
Anna Bagó-MasResearch Group of Clinical Anatomy, Embryology and Neuroscience (NEOMA), Department of Medical Sciences, University of Girona, Girona, Catalonia 17003, Spain.
Enrique VerdúResearch Group of Clinical Anatomy, Embryology and Neuroscience (NEOMA), Department of Medical Sciences, University of Girona, Girona, Catalonia 17003, Spain.
Victoria SalvadóDepartment of Chemistry, Faculty of Science, University of Girona, 17071 Girona, Catalonia, Spain.ORCID 0000-0002-1171-141X
Pere Boadas-VaelloResearch Group of Clinical Anatomy, Embryology and Neuroscience (NEOMA), Department of Medical Sciences, University of Girona, Girona, Catalonia 17003, Spain.ORCID 0000-0001-8497-1207

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathological pain subtypes can be classified as either neuropathic pain, caused by a somatosensory nervous system lesion or disease, or nociplastic pain, which develops without evidence of somatosensory system damage. Since there is no gold standard for the diagnosis of pathological pain subtypes, the proper classification of individual patients is currently an unmet challenge for clinicians. While the determination of specific biomarkers for each condition by current biochemical techniques is a complex task, the use of multimolecular techniques, such as matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS), combined with artificial intelligence allows specific fingerprints for pathological pain-subtypes to be obtained, which may be useful for diagnosis. We analyzed whether the information provided by the mass spectra of serum samples of four experimental models of neuropathic and nociplastic pain combined with their functional pain outcomes could enable pathological pain subtype classification by artificial neural networks. As a result, a simple and innovative clinical decision support method has been developed that combines MALDI-TOF MS serum spectra and pain evaluation with its subsequent data analysis by artificial neural networks and allows the identification and classification of pathological pain subtypes in experimental models with a high level of specificity.

Indexed as

Artificial IntelligenceNeural Networks, ComputerHumansPainSpectrometry, Mass, Matrix-Assisted Laser Desorption-Ionizationartificial intelligencediagnosticsfibromyalgiaMALDI-TOF MSmass spectrometryneuropathic pain

Identifiers

PMID36584284
PMCPMC9853500

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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.