Evidence map›Paper›PMID 33861812›Full record

ArticlePloS one2021

A dose-dependent beneficial effect of methotrexate on the risk of interstitial lung disease in rheumatoid arthritis patients.

Joanna Kur-Zalewska, Bartłomiej Kisiel, Marta Kania-Pudło, Małgorzata Tłustochowicz, Andrzej Chciałowski, Witold Tłustochowicz

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-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

7 citing papers in PubMed, 15 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Joanna Kur-ZalewskaDepartment of Internal Diseases and Rheumatology, Military Institute of Medicine, Warsaw, Poland.ORCID 0000-0001-8954-9144
Bartłomiej KisielDepartment of Internal Diseases and Rheumatology, Military Institute of Medicine, Warsaw, Poland.
Marta Kania-PudłoDepartment of Radiology, Military Institute of Medicine, Warsaw, Poland.
Małgorzata TłustochowiczDepartment of Internal Diseases and Rheumatology, Military Institute of Medicine, Warsaw, Poland.
Andrzej ChciałowskiDepartment of Infectious Diseases and Allergology, Military Institute of Medicine, Warsaw, Poland.
Witold TłustochowiczDepartment of Internal Diseases and Rheumatology, Military Institute of Medicine, Warsaw, Poland.
Wojskowy Instytut Medycyny Lotniczej · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe aim of the study was to assess the influence of different factors, including treatment, on the risk of ILD in the course of RA.

methodsA total of 109 RA patients were included in the analysis. High-resolution computed tomography (HRCT) of chest was obtained in each patient. Patients were classified as having ILD (ILD group) or not (N-ILD group). The ILD was graded using the semi-quantitative Warrick scale of fibrosis. Warrick extent score (WES) and Warrick severity score (WSS) were calculated separately for each patient, then combined to obtain a global score (WGS).

resultsIn univariate analysis the presence of ILD was associated positively with age (P = 5x10-6) and negatively with MTX treatment (P = 0.0013), mean MTX dose per year of treatment (P = 0.003) and number of DMARDs used (P = 0.046). On multivariate analysis only age and treatment with MTX were independently associated with the presence of ILD. WGS was significantly lower in patients treated with MTX in a dose of ≥15 mg/week (MTX≥15 group) as compared to patients treated with lower doses of MTX (0<MTX<15 group) or not treated with MTX (N-MTX group) (P = 0.04 and P = 0.037, respectively). The ILD prevalence was higher in N-MTX group than in 0<MTX<15 group (P = 0.0036) and MTX≥15 group (0.0007). The difference in ILD prevalence between MTX≥15 and 0<MTX<15 groups was not significant, but the latter group had higher WES (P = 0.044) and trended to have higher WSS and WGS. CONSCLUSIONS: We found a beneficial effect of MTX on RA-ILD. Importantly, this effect seems to be dose dependent.

Indexed as

AgedAntirheumatic AgentsArthritis, RheumatoidFemaleHumansLung Diseases, InterstitialMaleMethotrexateMiddle AgedAntirheumatic AgentsMethotrexate

Identifiers

PMID33861812
PMCPMC8051807
OpenAlexW3154199660

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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.