Evidence map›Paper›PMID 41310094›Full record

ArticleClinical rheumatology2026

Characteristics of patients with major relapse in giant cell arteritis: a multicenter case-control study.

Alice Rubinsztajn, Simon Parreau, Laurent Sailler, Hubert de Boysson, Olivier Espitia, Pascal Sève, Arnaud Hot, Laurent Perard, Jean-Christophe Lega, Sabine Mainbourg and 1 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Clinical rheumatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Alice RubinsztajnService de Médecine Interne Et Pathologies Vasculaires, Centre Hospitalier Lyon Sud, Hospices Civils de Lyon, 69495, Pierre-Bénite, France.ORCID http://orcid.org/0000-0001-8997-6592
Simon ParreauService de Médecine Interne, Centre Hospitalier Universitaire Dupuytren, 87042, Limoges, France.
Laurent SaillerService de Médecine Interne, Centre Hospitalier Universitaire de Toulouse, 31300, Toulouse, France.
Hubert de BoyssonService de Médecine Interne, Centre Hospitalier Universitaire de Caen, 14000, Caen, France.
Olivier EspitiaDépartement de Médecine Interne Et Vasculaire, L'institut du Thorax, UMR1087/CNRS UMR 6291, Université de Nantes, Centre Hospitalier Universitaire de Nantes, INSERM, Team III Vascular & Pulmonary Diseases, 44000, Nantes, France.
Pascal SèveService de Médecine Interne, Centre Hospitalier Universitaire de La Croix-Rousse, Hospices Civils de Lyon, 69004, Lyon, France.
Arnaud HotService de Médecine Interne, Centre Hospitalier Universitaire Edouard Herriot, Hospices Civils de Lyon, 69003, Lyon, France.
Laurent PerardService de Médecine Interne, Centre Hospitalier St-Joseph St-Luc, 69007, Lyon, France.
Jean-Christophe LegaService de Rhumatologie, Centre Hospitalier Lyon Sud, Hospices Civils de Lyon, 69495, Pierre-Bénite, France.ORCID http://orcid.org/0000-0002-9398-2968
Sabine MainbourgService de Médecine Interne Et Pathologies Vasculaires, Centre Hospitalier Lyon Sud, Hospices Civils de Lyon, 69495, Pierre-Bénite, France. sabine.mainbourg@chu-lyon.fr.ORCID http://orcid.org/0000-0003-4564-2931
and the French Large Vessel Arteritis Study Group (GEFA)

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe objective was to identify predictive factors for major relapses (MR) in patients with giant cell arteritis (GCA) and to compare clinical characteristics between MR phenotypes.

methodThis multicenter retrospective case-control study included patients fulfilling GiaCTA criteria for GCA. Cases were patients experiencing MR according to 2018 EULAR definitions. Controls were GCA patients without MR with a 1:3 ratio. Data were collected and analyzed using univariate and multivariate logistic regression to determine factors independently associated with MR. MR was subclassified into cranial-MR and large-vessel-MR which were compared using appropriate statistical tests.

results258 patients were included, 70 cases and 188 controls (48.4% minor relapse, and 24.4% without relapse). The mean age at diagnosis was 72.5 ± 8.6 years, 70,9% were females. Younger age at diagnosis was associated with an increased risk of MR (OR = 0.93 per 10 years, 95% CI [0.87; 0.999], p = 0.043). No other clinically significant risk factors were identified. Among the 70 cases, 48.6% had a cranial-MR and 51.4% a large-vessel-MR. Patients with a cranial-MR were older (74.3 ± 6.3 years vs. 67.3 ± 7.0 years, p < 0.001) and were more likely to have cranial symptoms at diagnosis of GCA (91.2% vs. 69.4%, p = 0.023) compared to those with a large-vessel-MR. Compared with cranial-MR, large-vessel MR was more frequent in women (80.5% vs. 52.9%, p < 0.01) and tended to be associated with aortitis at diagnosis (70.0% vs. 43.5%, p = 0.052).

conclusionsYounger age at diagnosis was the only independent predictor of MR. Relapse patterns mirrored initial disease phenotype, supporting the existence of cranial and large-vessel GCA subtypes. Key Points •Younger age at diagnosis is associated with a higher risk of major relapse in giant cell arteritis. •Cranial and large-vessel major relapses display distinct clinical patterns, often mirroring the initial disease phenotype. •No strong laboratory or imaging predictor of major relapse was identified in this multicentre case-control study.

Indexed as

Giant Cell ArteritisAgedAged, 80 and overAge FactorsCase-Control StudiesFemaleHumansLogistic ModelsMaleMiddle AgedRecurrenceRetrospective StudiesRisk FactorsAortitisGiant cell arteritisHumansIschemiaRecurrenceRisk factors

Identifiers

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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.