Evidence map›Paper›PMID 31970657›Full record

ArticleMolecular neurobiology2020

Antioxidant and Anti-inflammatory Diagnostic Biomarkers in Multiple Sclerosis: A Machine Learning Study.

Leda Mezzaroba, Andrea Name Colado Simão, Sayonara Rangel Oliveira, Tamires Flauzino, Daniela Frizon Alfieri, Wildea Lice de Carvalho Jennings Pereira, Ana Paula Kallaur, Marcell Alysson Batisti Lozovoy, Damacio Ramón Kaimen-Maciel, Michael Maes and 1 more

Abstract readValidation Study
PubMed Publisher
In one paragraph

Article in Molecular neurobiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 2 pooled it
4.2field-weighted citation impact, top 5% 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

22 citing papers in PubMed, 2 syntheses or guidelines pooled it, 50 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. A framework for blood biomarker discovery in MS.Multiple sclerosis (Houndmills, Basingstoke, England) · 2026
    Review
  5. Rethinking MS Therapeutics: From Disease Pathogenesis Mechanisms to AI-Driven Drug Discovery.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Artificial Intelligence and Multiple Sclerosis.Current neurology and neuroscience reports · 2024
    Review
  10. Review
  11. Oxidative Stress Markers in Multiple Sclerosis.International journal of molecular sciences · 2024
    Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. 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 2 institutions in 3 countries.

Leda MezzarobaLaboratory of Research in Applied Immunology, University of Londrina, Paraná, Brazil.
Andrea Name Colado SimãoDepartment of Pathology, Clinical Analysis and Toxicology, Health Sciences Center, University of Londrina, Av. Robert Koch 60, CEP, Paraná, 86038-350, Brazil.
Sayonara Rangel OliveiraDepartment of Pathology, Clinical Analysis and Toxicology, Health Sciences Center, University of Londrina, Av. Robert Koch 60, CEP, Paraná, 86038-350, Brazil.
Tamires FlauzinoLaboratory of Research in Applied Immunology, University of Londrina, Paraná, Brazil.
Daniela Frizon AlfieriLaboratory of Research in Applied Immunology, University of Londrina, Paraná, Brazil.
Wildea Lice de Carvalho Jennings PereiraLaboratory of Research in Applied Immunology, University of Londrina, Paraná, Brazil.
Ana Paula KallaurLaboratory of Research in Applied Immunology, University of Londrina, Paraná, Brazil.
Marcell Alysson Batisti LozovoyDepartment of Pathology, Clinical Analysis and Toxicology, Health Sciences Center, University of Londrina, Av. Robert Koch 60, CEP, Paraná, 86038-350, Brazil.
Damacio Ramón Kaimen-MacielOutpatient Demyelinating Diseases, University of Londrina, Londrina, Paraná, Brazil.
Michael MaesImpact Strategic Research Centre, School of Medicine, Deakin University, Geelong, Victoria, Australia.
Edna Maria Vissoci ReicheDepartment of Pathology, Clinical Analysis and Toxicology, Health Sciences Center, University of Londrina, Av. Robert Koch 60, CEP, Paraná, 86038-350, Brazil. reiche@sercomtel.com.br.ORCID http://orcid.org/0000-0001-6507-2839
Universidade Estadual de Londrina · BRDeakin University · AU

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior Finance Code 001.
6 · The paper itself

Abstract

An imbalance of inflammatory/anti-inflammatory and oxidant/antioxidant molecules has been implicated in the demyelination and axonal damage in multiple sclerosis (MS). The current study aimed to evaluate the plasma levels of tumor necrosis factor (TNF)-α, soluble TNF receptor (sTNFR)1, sTNFR2, adiponectin, hydroperoxides, advanced oxidation protein products (AOPP), nitric oxide metabolites, total plasma antioxidant capacity using the total radical-trapping antioxidant parameter (TRAP), sulfhydryl (SH) groups, as well as serum levels of zinc in 174 MS patients and 182 controls. The results show that MS is characterized by lowered levels of zinc, adiponectin, TRAP, and SH groups and increased levels of AOPP. MS was best predicted by a combination of lowered levels of zinc, adiponectin, TRAP, and SH groups yielding an area under the receiver operating characteristic (AUC/ROC) curve of 0.986 (±0.005). The combination of these four antioxidants with sTNFR2 showed an AUC/ROC of 0.997 and TRAP, adiponectin, and zinc are the most important biomarkers for MS diagnosis followed at a distance by sTNFR2. Support vector machine with tenfold validation performed on the four antioxidants showed a training accuracy of 92.9% and a validation accuracy of 90.6%. The results indicate that lowered levels of those four antioxidants are associated with MS and that these antioxidants are more important biomarkers of MS than TNF-α signaling and nitro-oxidative biomarkers. Adiponectin, TRAP, SH groups, zinc, and sTNFR2 play a role in the pathophysiology of MS, and a combination of these biomarkers is useful for predicting MS with high sensitivity, specificity, and accuracy. Drugs that increase the antioxidant capacity may offer novel therapeutic opportunities for MS.

Indexed as

Neural Networks, ComputerSupport Vector MachineAdiponectinAdultAdvanced Oxidation Protein ProductsAntioxidantsBiomarkersFemaleHumansInflammationMaleMiddle AgedMultiple SclerosisNitric OxideNitrosative StressOxidation-ReductionAdiponectinADIPOQ protein, humanAdvanced Oxidation Protein ProductsAntioxidantsBiomarkersNitric OxideReceptors, Tumor Necrosis FactorSulfhydryl CompoundsTumor Necrosis Factor-alphaAdiponectinMachine learning studyMultiple sclerosisOxidative stressTNF receptorsZinc

Identifiers

PMID31970657
OpenAlexW3002843465

What OpenQuestion holds

Textmetadata
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.