Evidence map›Paper›PMID 40682289›Full record

ArticleInternational journal of immunopathology and pharmacology

Galectin-1 as a potential biomarker of rheumatoid arthritis drug effectiveness.

Nikola Krstić, Tatjana Jevtović Stoimenov, Sonja Stojanović, Branka Đorđević, Ivana Damnjanović

Abstract read
In one paragraph

Article in International journal of immunopathology and pharmacology. 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. Observational
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.

Nikola KrstićFaculty of Medicine, University of Niš, Niš, Serbia.ORCID 0000-0002-4398-1449
Tatjana Jevtović StoimenovDepartment of Biochemistry, Faculty of Medicine, University of Niš, Niš, Serbia.ORCID 0000-0003-0600-5411
Sonja StojanovićDepartment of Internal Medicine and Patient Care, Faculty of Medicine, University of Niš, Niš, Serbia.ORCID 0000-0002-6400-1411
Branka ĐorđevićDepartment of Biochemistry, Faculty of Medicine, University of Niš, Niš, Serbia.ORCID 0000-0002-4521-1253
Ivana DamnjanovićDepartment of Pharmacy, Faculty of Medicine, University of Niš, Niš, Serbia.ORCID 0000-0003-0079-8457

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The treatment approach to RA has changed over time, but the main goal of treatment has remained the same, that is, achieving disease remission. Given the lack of RA disease activity tools and biomarkers that can reliably predict RA drug effectiveness not just on joints but also on extra-articular manifestations. The involvement of galectins, especially Galectin-1 (Gal1) in the regulation of immune regulation makes them potential good candidate non-specific biomarkers of autoimmune diseases like RA. Examining the possibility of applying Gal1 as a potential biomarker for evaluating the effectiveness of therapy. A quasi-experimental study was conducted to assess changes in serum Gal1 concentrations in patients with RA, compared with a healthy control group. The study included a total of 88 participants, consisting of 48 patients diagnosed with RA and 40 healthy voluntary blood donors. Patients were enrolled in the study based on a selective recruitment process, provided they met the criteria outlined in the Inclusion Criteria section. The diagnosis of RA was established by physicians in accordance with the ACR/EULAR2010 classification criteria. The collected samples were subjected to concentration determination using a commercial ELISA kit for human Gal1. The serum Gal1 concentration of the examined groups differed significantly (

Indexed as

Antirheumatic AgentsArthritis, RheumatoidGalectin 1AdultAgedBiomarkersCase-Control StudiesFemaleHumansMaleMiddle AgedTreatment OutcomeAntirheumatic AgentsBiomarkersGalectin 1LGALS1 protein, humangalectin 1new biomarkerrheumatoid arthritistherapy

Identifiers

PMID40682289
PMCPMC12276510

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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.