Evidence map›Paper›PMID 40971971›Full record

ArticleRheumatology (Oxford, England)2026

Methylprednisolone plus MTX-based regime vs prednisone-based standard of care for GCA: a propensity score study.

Adriana Soto-Peleteiro, José Hernández-Rodríguez, Fátima Raad, Borja de Miguel, Leonor Acha, Marina Torio, Halbert Hernandez-Negrin, Verónica Gómez-Caverzaschi, Ioana Ruiz-Arruza, Olga Araujo and 4 more

Abstract readMulticenter StudyComparative Study
In one paragraph

Article in Rheumatology (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Management of glucocorticoid-induced osteoporosis in rheumatic diseases.Best practice & research. Clinical rheumatology · 2026
    Review
  2. 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

14 authors.

Adriana Soto-PeleteiroBiobizkaia Health Research Institute, Autoimmune Diseases Research Unit, Hospital Universitario Cruces, Bizkaia, Spain.ORCID 0000-0001-8959-8683
José Hernández-RodríguezVasculitis Research Unit, Department of Autoimmune Diseases, Hospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.ORCID 0000-0002-2357-2015
Fátima RaadVasculitis Research Unit, Department of Autoimmune Diseases, Hospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.ORCID 0009-0008-7923-5422
Borja de MiguelDepartment of Internal Medicine, Hospital Universitario 12 de Octubre, Madrid, Spain.ORCID 0000-0001-7105-9470
Leonor AchaBiobizkaia Health Research Institute, Autoimmune Diseases Research Unit, Hospital Universitario Cruces, Bizkaia, Spain.
Marina TorioBiobizkaia Health Research Institute, Autoimmune Diseases Research Unit, Hospital Universitario Cruces, Bizkaia, Spain.
Halbert Hernandez-NegrinBiobizkaia Health Research Institute, Autoimmune Diseases Research Unit, Hospital Universitario Cruces, Bizkaia, Spain.ORCID 0000-0002-9992-9148
Verónica Gómez-CaverzaschiVasculitis Research Unit, Department of Autoimmune Diseases, Hospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.ORCID 0000-0001-5242-6925
Ioana Ruiz-ArruzaBiobizkaia Health Research Institute, Autoimmune Diseases Research Unit, Hospital Universitario Cruces, Bizkaia, Spain.ORCID 0000-0002-9628-4022
Olga AraujoVasculitis Research Unit, Department of Autoimmune Diseases, Hospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.ORCID 0000-0003-1763-1880
Sergio Prieto-GonzálezVasculitis Research Unit, Department of Autoimmune Diseases, Hospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.ORCID 0000-0003-3179-597X
Georgina Espígol-FrigoléVasculitis Research Unit, Department of Autoimmune Diseases, Hospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.ORCID 0000-0002-8299-0209
Maria C CidVasculitis Research Unit, Department of Autoimmune Diseases, Hospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.ORCID 0000-0002-4730-0938
Guillermo Ruiz-IrastorzaBiobizkaia Health Research Institute, Autoimmune Diseases Research Unit, Hospital Universitario Cruces, Bizkaia, Spain.ORCID 0000-0001-7788-1043

Funding

Department of Education of the Basque Government
6 · The paper itself

Abstract

objectivesTreatment of GCA still requires substantial exposure to glucocorticoids (GCs), which are associated with significant toxicity. This study compares the efficacy and safety of the GC-only standard of care (SOC) with a regimen combining intravenous methylprednisolone (IVMP) pulses, MTX and lower doses of prednisone, in newly diagnosed patients with GCA.

methodsA usual clinical practice study was conducted in three Spanish academic hospitals. One hundred and fifty-one patients diagnosed with GCA were treated with SOC prednisone (40-60 mg/d) or with IVMP (125-500 mg/d ×3) followed by lower-dose prednisone (≤30 mg/d) and MTX (IVMP/MTX), with a follow-up of 2 years. A propensity score was used to adjust for baseline differences in the multivariate analyses.

resultsSeventy-nine (52.3%) patients received SOC prednisone and 72 (47.7%) IVMP/MTX. The clinical characteristics at baseline were similar in both the groups. Hundred percent patients achieved remission after a median time of 4 weeks, without differences between the groups. Relapse rates were also similar. Patients receiving IVMP/MTX had significantly lower cumulative GC doses and reached prednisone ≤5 mg/d faster than SOC patients (mean 13.8 vs 56.5 weeks; P < 0.001). Patients in the IVMP/MTX group were less likely to suffer any GC-related adverse effect (adjusted OR 0.35, 95% CI 0.14-0.85; P = 0.021).

conclusionsThe combination IVMP/MTX with lower-dose prednisone is as effective as the SOC in inducing remission and preventing relapses in GCA. The IVMP/MTX scheme significantly reduces GC exposure and GC-associated adverse effects. IVMP/MTX could be a potential GC-sparing strategy, especially in patients with GCA at higher risk of GC toxicity.

Indexed as

GlucocorticoidsMethotrexateMethylprednisolonePrednisoneAgedAged, 80 and overDrug Therapy, CombinationFemaleHumansMaleMiddle AgedPropensity ScoreRemission InductionStandard of CareTreatment OutcomeGlucocorticoidsMethotrexateMethylprednisolonePrednisonecataractsglucocorticoidsinfectionsosteonecrosisosteoporosisremissionside effectsvasculitis

Identifiers

PMID40971971
PMCPMC12862367

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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.