Evidence map›Paper›PMID 31842970›Full record

ArticleArthritis research & therapy2019

Protein profiling and network enrichment analysis in individuals before and after the onset of rheumatoid arthritis.

Mikael Brink, Anders Lundquist, Andrey Alexeyenko, Kristina Lejon, Solbritt Rantapää-Dahlqvist

Open access · goldAbstract read
In one paragraph

Article in Arthritis research & therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

8 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Pathogenic Role of Cytokines in Rheumatoid Arthritis.Journal of clinical medicine · 2025
    Review
  4. Review
  5. Role of IFN-α in Rheumatoid Arthritis.Current rheumatology reports · 2024
    Review
  6. Article
  7. Article
  8. 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

5 authors at 2 institutions in 1 country.

Mikael BrinkDepartment of Public Health and Clinical Medicine, Rheumatology, Umeå University, 901 87, Umeå, Sweden. mikael.brink@umu.se.ORCID 0000-0001-7675-3488
Anders LundquistDepartment of Clinical Microbiology, Division of Infection and Immunology, Umeå University, 901 87, Umeå, Sweden.
Andrey AlexeyenkoScience for Life Laboratory, Department of Microbiology, Tumor and Cell Biology (MTC), Karolinska Institutet, Stockholm, Sweden.
Kristina LejonDivision of Infection and Immunology, Department of Clinical Microbiology, Umeå University, Umeå, Sweden.
Solbritt Rantapää-DahlqvistDepartment of Public Health and Clinical Medicine, Rheumatology, Umeå University, 901 87, Umeå, Sweden.
Umeå University · SEScience for Life Laboratory · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAntibodies and upregulated cytokines and chemokines predate the onset of rheumatoid arthritis (RA) symptoms. We aimed to identify the pathways related to the early processes leading to RA development, as well as potential novel biomarkers, using multiple protein analyses.

methodsA case-control study was conducted within the Biobank of northern Sweden. The plasma samples from 118 pre-symptomatic individuals (207 samples; median predating time 4.1 years), 79 early RA patients, and 74 matched controls were analyzed. The levels of 122 unique proteins with an acknowledged relationship to autoimmunity were analyzed using 153 antibodies and a bead-based multiplex system (FlexMap3D; Luminex Corp.). The data were analyzed using multifactorial linear regression model, random forest, and network enrichment analysis (NEA) based on the 10 most significantly differentially expressed proteins for each two-by-two group comparison, using the MSigDB collection of hallmarks.

resultsThere was a high agreement between the different statistical methods to identify the most significant proteins. The adipogenesis and interferon alpha response hallmarks differentiated pre-symptomatic individuals from controls. These two hallmarks included proteins involved in innate immunity. Between pre-symptomatic individuals and RA patients, three hallmarks were identified as follows: apical junction, epithelial mesenchymal transition, and TGF-β signaling, including proteins suggestive of cell interaction, remodulation, and fibrosis. The adipogenesis and heme metabolism hallmarks differentiated RA patients from controls.

conclusionsWe confirm the importance of interferon alpha signaling and lipids in the early phases of RA development. Network enrichment analysis provides a tool for a deeper understanding of molecules involved at different phases of the disease progression.

Indexed as

Protein Interaction MapsAgedArthritis, RheumatoidBiomarkersCase-Control StudiesFemaleGene Regulatory NetworksHumansInterferon-alphaLipidsMaleMiddle AgedProtein BindingProteomeProteomicsSignal TransductionBiomarkersInterferon-alphaLipidsProteomePlasma biomarkersPre-symptomatic stageProtein levelsRheumatoid arthritis

Identifiers

PMID31842970
PMCPMC6915963
OpenAlexW2995898955

What Socratic holds

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LicenceCC BY
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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 Socratic graph.