Evidence map›Paper›PMID 30615300›Full record

ArticleArthritis & rheumatology (Hoboken, N.J.)2019

Profiling of Gene Expression Biomarkers as a Classifier of Methotrexate Nonresponse in Patients With Rheumatoid Arthritis.

Darren Plant, Mateusz Maciejewski, Samantha Smith, Nisha Nair, Maximising Therapeutic Utility in Rheumatoid Arthritis Consortium, the RAMS Study Group, Kimme Hyrich, Daniel Ziemek, Anne Barton, Suzanne Verstappen

Abstract read
In one paragraph

Article in Arthritis & rheumatology (Hoboken, N.J.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing 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

41 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Role of IFN-α in Rheumatoid Arthritis.Current rheumatology reports · 2024
    Review
  10. Review
  11. Review
  12. Towards Personalized Medicine in Rheumatoid Arthritis.Open access rheumatology : research and reviews · 2024
    Review
  13. Differences in IDO1Frontiers in immunology · 2024
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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.

Darren PlantManchester University NHS Foundation Trust, Manchester, UK.
Mateusz MaciejewskiPfizer, Cambridge, Massachusetts.
Samantha SmithUniversity of Manchester, Manchester, UK.
Nisha NairUniversity of Manchester, Manchester, UK.
Maximising Therapeutic Utility in Rheumatoid Arthritis Consortium, the RAMS Study Group
Kimme HyrichManchester University NHS Foundation Trust, Manchester, UK.
Daniel ZiemekPfizer, Cambridge, Massachusetts.
Anne BartonManchester University NHS Foundation Trust, Manchester, UK.
Suzanne VerstappenManchester University NHS Foundation Trust, Manchester, UK.

Funding

Arthritis Research UK 20380Arthritis Research UK 20385Arthritis Research UK 20670Medical Research Council MR/K015346/1Pfizer I-CRP
6 · The paper itself

Abstract

objectiveApproximately 30-40% of rheumatoid arthritis (RA) patients who are initially started on low-dose methotrexate (MTX) will not benefit from the treatment. To date, no reliable biomarkers of MTX inefficacy in RA have been identified. The aim of this study was to analyze whole blood samples from RA patients at 2 time points (pretreatment and 4 weeks following initiation of MTX), to identify gene expression biomarkers of the MTX response.

methodsRA patients who were about to commence treatment with MTX were selected from the Rheumatoid Arthritis Medication Study. Using European League Against Rheumatism (EULAR) response criteria, 42 patients were categorized as good responders and 43 as nonresponders at 6 months following the initation of MTX treatment. Data on whole blood transcript expression were generated, and supervised machine learning methods were used to predict a EULAR nonresponse. Models in which transcript levels were included were compared to models in which clinical covariates alone (e.g., baseline disease activity, sex) were included. Gene network and ontology analysis was also performed.

resultsBased on the ratio of transcript values (i.e., the difference in log

conclusionTesting for changes in gene expression between pretreatment and 4 weeks post-treatment initiation may provide an early classifier of the MTX treatment response in RA patients who are unlikely to benefit from MTX over 6 months. Such patients should, therefore, have their treatment escalated more rapidly, which would thus potentially impact treatment pathways. These findings emphasize the importance of a role for early treatment biomarker monitoring in RA patients started on MTX.

Indexed as

TranscriptomeAdultAgedAntirheumatic AgentsArthritis, RheumatoidFemaleGene Expression ProfilingGene Regulatory NetworksHumansInterferon Type IMaleMethotrexateMiddle AgedSignal TransductionTreatment FailureAntirheumatic AgentsInterferon Type IMethotrexate

Identifiers

PMID30615300
PMCPMC9328381

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.