Evidence map›Paper›PMID 37973683›Full record

ArticleLung2023

Methotrexate Polyglutamate Concentrations as a Possible Predictive Marker for Effectiveness of Methotrexate Therapy in Patients with Sarcoidosis: A Pilot Study.

Montse Janssen Bonás, Janani Sundaresan, Ruth G M Keijsers, Eduard A Struys, Bas J M Peters, Vivienne Kahlmann, Marlies S Wijsenbeek, Maurits C F J de Rotte, Jan C Grutters, Marcel Veltkamp

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In one paragraph

Article in Lung, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. New Therapies for Sarcoidosis: Molecular and Pathophysiological Basis.International journal of molecular sciences · 2026
    Review
  2. Article
  3. 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

10 authors at 5 institutions in 1 country.

Montse Janssen BonásDepartment of Pulmonology, ILD Center of Excellence, St. Antonius Hospital, Nieuwegein, The Netherlands.
Janani SundaresanDepartment of Clinical Chemistry, Amsterdam University Medical Center, Amsterdam, The Netherlands.
Ruth G M KeijsersDepartment of Nuclear Medicine, St. Antonius Hospital, Nieuwegein, Utrecht, The Netherlands.
Eduard A StruysDepartment of Clinical Chemistry, Amsterdam University Medical Center, Amsterdam, The Netherlands.
Bas J M PetersDepartment of Clinical Pharmacy, St. Antonius Hospital, Nieuwegein, Utrecht, The Netherlands.
Vivienne KahlmannCenter of Excellence for ILD and Sarcoidosis, Erasmus Medical Center, Rotterdam, The Netherlands.
Marlies S WijsenbeekCenter of Excellence for ILD and Sarcoidosis, Erasmus Medical Center, Rotterdam, The Netherlands.
Maurits C F J de RotteDepartment of Clinical Chemistry, Amsterdam University Medical Center, Amsterdam, The Netherlands.
Jan C GruttersDepartment of Pulmonology, ILD Center of Excellence, St. Antonius Hospital, Nieuwegein, The Netherlands.
Marcel VeltkampDepartment of Pulmonology, ILD Center of Excellence, St. Antonius Hospital, Nieuwegein, The Netherlands. m.veltkamp@antoniusziekenhuis.nl.
Amsterdam University Medical Centers · NLSt. Antonius Ziekenhuis · NLCancer Genomics Centre · NLUniversity Medical Center Utrecht · NLUtrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMethotrexate (MTX), a folate antagonist, is often used as second-line treatment in patients with sarcoidosis. Effectiveness of MTX has large inter-patient variability and at present therapeutic drug monitoring (TDM) of MTX is not possible. Upon administration, MTX is actively transported into cells and metabolized to its active forms by adding glutamate residues forming MTXPG

methodsWe retrospectively included patients with sarcoidosis that had started on MTX therapy and from whom blood samples and FDG-PET/CT were available 3 and 6-12 months after MTX initiation, respectively. FDG-uptake was measured by SUVmax in the heart, lungs and thoracic lymph nodes. Changes in SUVmax was used to determine anti-inflammatory response after 6-12 months of MTX therapy. MTXPG

resultsWe included 42 sarcoidosis patients treated with MTX (15 mg/week); 31 with cardiac sarcoidosis and 11 with pulmonary sarcoidosis. In MTXPG

conclusionThese results suggest a relation between MTXPG

Indexed as

MethotrexateSarcoidosisAnti-Inflammatory AgentsChromatography, LiquidFluorodeoxyglucose F18HumansPilot ProjectsPolyglutamic AcidPositron Emission Tomography Computed TomographyRetrospective StudiesTandem Mass SpectrometryAnti-Inflammatory AgentsFluorodeoxyglucose F18Methotrexatemethotrexate polyglutamatePolyglutamic AcidMethotrexatePolyglutamatesSarcoidosisTreatment response

Identifiers

PMID37973683
OpenAlexW4388728557

What OpenQuestion holds

Textmetadata
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.