Evidence map›Paper›PMID 34299006›Full record

ArticleInternational journal of molecular sciences2021

Disease Differentiation and Monitoring of Anti-TNF Treatment in Rheumatoid Arthritis and Spondyloarthropathies.

Katarzyna Bogunia-Kubik, Wojciech Wojtowicz, Jerzy Swierkot, Karolina Anna Mielko, Badr Qasem, Joanna Wielińska, Renata Sokolik, Łukasz Pruss, Piotr Młynarz

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. 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

9 authors.

Katarzyna Bogunia-KubikLaboratory of Clinical Immunogenetics and Pharmacogenetics, Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, 53-114 Wroclaw, Poland.
Wojciech WojtowiczDepartment of Bioorganic Chemistry, Wroclaw University of Technology, 50-370 Wroclaw, Poland.ORCID 0000-0001-6906-3120
Jerzy SwierkotDepartment of Rheumatology and Internal Medicine, Wroclaw Medical University, 50-556 Wroclaw, Poland.
Karolina Anna MielkoDepartment of Bioorganic Chemistry, Wroclaw University of Technology, 50-370 Wroclaw, Poland.
Badr QasemDepartment of Bioorganic Chemistry, Wroclaw University of Technology, 50-370 Wroclaw, Poland.ORCID 0000-0001-7085-0287
Joanna WielińskaLaboratory of Clinical Immunogenetics and Pharmacogenetics, Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, 53-114 Wroclaw, Poland.
Renata SokolikDepartment of Rheumatology and Internal Medicine, Wroclaw Medical University, 50-556 Wroclaw, Poland.
Łukasz PrussDepartment of Bioorganic Chemistry, Wroclaw University of Technology, 50-370 Wroclaw, Poland.ORCID 0000-0002-7223-9382
Piotr MłynarzDepartment of Bioorganic Chemistry, Wroclaw University of Technology, 50-370 Wroclaw, Poland.ORCID 0000-0002-8502-4022

Funding

Narodowym Centrum Nauki 2016/21/B/NZ5/01901
6 · The paper itself

Abstract

Rheumatoid arthritis (RA), ankylosing spondylitis (AS), and psoriatic arthritis (PsA) are comprehensive immunological disorders. The treatment of these disorders is limited to ameliorating the symptoms and improving the quality of life of patients. In this study, serum samples from RA, AS, and PsA patients were analyzed with metabolomic tools employing the 1H NMR method in combination with univariate and multivariate analyses. The results obtained in this study showed that the changes in metabolites were the highest for AS > RA > PsA. The study demonstrated that the time until remission or until low disease activity is achieved is shortest (approximately three months) for AS, longer for RA and longest for PsA. The statistically common metabolite that was found to be negatively correlated with the healing processes of these disorders is ethanol, which may indicate the involvement of the gut microflora and/or the breakdown of malondialdehyde as a cell membrane lipid peroxide product.

Indexed as

AdultArthritis, PsoriaticArthritis, RheumatoidCohort StudiesComputational BiologyEthanolFemaleHumansMagnetic Resonance SpectroscopyMaleMetabolomePrincipal Component AnalysisSpondylitis, AnkylosingTumor Necrosis Factor InhibitorsEthanolTumor Necrosis Factor Inhibitorsankylosing spondylitisbiological treatment outcomemetabolomicspsoriatic arthritisrheumatoid arthritis

Identifiers

PMID34299006
PMCPMC8307996

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Registered trials

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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.