Evidence map›Paper›PMID 41475838›Full record

ArticleRMD open2025

Concordance between presenting features and relapse in granulomatosis with polyangiitis: implications for risk assessment and counselling.

Michele Iudici, Zubeyir Salis, Pascal Cohen, Antoine Néel, Achille Aouba, Francois Lifermann, Marc Ruivard, Olivier Aumaître, Bernard Bonnotte, Maxime Samson and 15 more

Abstract read
In one paragraph

Article in RMD open, 2025. 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
–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

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

25 authors.

Michele IudiciDivision of rheumatology, Geneva University Hospitals and University of Geneva, Geneva, Switzerland Michele.iudici@hug.ch xavier.puechal@aphp.fr.ORCID 0000-0001-5871-8806
Zubeyir SalisUniversity of Montpellier, Montpellier, France.
Pascal CohenDepartment of Internal Medicine, Cochin Hospital, National Referral Center for Rare Systemic Autoimmune and Autoinflammatory Diseases of Ile de France, East and West, Assistance Publique - Hôpitaux de Paris, Paris, France.
Antoine NéelDepartment of Internal Medicine, Nantes University Hospital, and Nantes Université, INSERM, Center for Research in Transplantation and Translational Immunology (CR2TI), UMR 1064, Nantes, France.
Achille AoubaDépartement de médecine interne, CHU Caen, Caen, France, Caen, France.
Francois LifermannDepartment of Internal Medicine, Dax Hospital, Dax, France.
Marc RuivardUniversité Clermont Auvergne, CNRS, CHU Clermont-Ferrand, Institut Pascal, F-63000, Clermont-Ferrand, France.
Olivier AumaîtreUniversité Clermont Auvergne, CNRS, CHU Clermont-Ferrand, Institut Pascal, F-63000, Clermont-Ferrand, France.
Bernard BonnotteDepartment of Internal Medicine and Clinical Immunology, Referral Center for Rare Systemic Autoimmune and Autoinflammatory Diseases, Dijon-Bourgogne University Hospital, University EPE Bourgogne Europe, Dijon, France.ORCID 0000-0001-7229-3808
Maxime SamsonDepartment of Internal Medicine and Clinical Immunology, Referral Center for Rare Systemic Autoimmune and Autoinflammatory Diseases, Dijon-Bourgogne University Hospital, University EPE Bourgogne Europe, Dijon, France.ORCID 0000-0002-6547-232X
Francois MaurierInternal Medicine, UNEOS Hospitals, Metz-Ventoux, Metz, France.
Thomas Le GallouInternal Medicine and Clinical Immunology, University of Rennes 1, Rennes, France.
Eric HachullaDepartment of Internal Medicine and Clinical immunology, National Referral Centre for Rare Systemic Auto-immune and auto-inflammatory Diseases, Univ. Lille, Inserm, CHU Lille, U1286 - INFINITE, University of Lille, Lille, France.
Alexandre KarrasNephrology, European Hospital Georges Pompidou, AP-HP, University Paris-Cité, Paris, France.
Vincent CottinNational Referral Center for Rare Pulmonary Diseases, Louis-Pradel Hospital, Claude-Bernard University Lyon 1, Lyon, France.ORCID 0000-0002-5591-0955
Noemie Jourde-ChicheAPHM, CHU de la Conception, Nephrology, Aix-Marseille Univ, C2VN, INSERM, INRAE, Marseille, France.ORCID 0000-0001-9315-1577
Jean-François ViallardInternal Medicine, Haut-Lévêque Hospital, University of Bordeaux, Bordeaux, France.
Amandine PerierDepartment of Internal Medicine, Niort Hospital, Niort, France.
Pascal GodmerInternal Medicine, Bretagne - Atlantique Hospital, Vannes, France.
Thomas QuéméneurNephrology and Internal Medicine, Valenciennes Hospital, Valenciennes, France.
Claire de MoreuilInternal Medicine, La Cavale Blanche University Hospital, Brest, France.ORCID 0000-0003-1142-0978
Loïc GuillevinDepartment of Internal Medicine, Cochin Hospital, National Referral Center for Rare Systemic Autoimmune and Autoinflammatory Diseases of Ile de France, East and West, Assistance Publique - Hôpitaux de Paris, Paris, France.
Benjamin TerrierDepartment of Internal Medicine, Cochin Hospital, National Referral Center for Rare Systemic Autoimmune and Autoinflammatory Diseases of Ile de France, East and West, Assistance Publique - Hôpitaux de Paris, Paris, France.ORCID 0000-0001-6612-7336
Xavier PuéchalDepartment of Internal Medicine, Cochin Hospital, National Referral Center for Rare Systemic Autoimmune and Autoinflammatory Diseases of Ile de France, East and West, Assistance Publique - Hôpitaux de Paris, Paris, France Michele.iudici@hug.ch xavier.puechal@aphp.fr.ORCID 0000-0003-3573-9203
French Vasculitis Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the concordance between organ involvement at diagnosis and relapse in granulomatosis with polyangiitis and factors associated with new disease features at relapse.

methodsData from a national database of newly diagnosed patients was analysed. Clinical features were recorded at diagnosis and relapse, grouped by organ system. ORs and HRs were used to assess associations between baseline features and first relapse. Factors independently associated with new organ involvement at relapse were identified using multivariable logistic regression.

resultsAmong 795 patients (median follow-up 3.5 years), 394 (50%) relapsed; organ involvement at relapse was available for 376 patients. Relapses most often affected ear, nose and throat (ENT), lungs and kidneys. Organ involvement at diagnosis was associated with a higher likelihood of relapse in the same organ: eyes (OR 6.69), lungs (OR 3.35), kidneys (OR 3.58), nervous system (OR 2.90), and mucocutaneous (OR 4.53). Major manifestations associated with a higher likelihood of recurrence were scleritis, pachymeningitis, subglottic stenosis and worsening renal function. For 56% of patients, the first relapse affected only the initially involved organs. Of the 165 patients with new organ manifestations, these were rarely isolated (n=34) and usually occurred alongside involvement of at least one previously affected organ (n=131). In multivariable analysis, systemic, ENT and lung manifestations at diagnosis were associated with a lower risk of new organ disease at relapse.

conclusionAlthough new features can still emerge, organ involvement at diagnosis is associated with a higher likelihood of relapse in the same organ.

Indexed as

Granulomatosis with PolyangiitisAdultAgedFemaleFollow-Up StudiesHumansMaleMiddle AgedRecurrenceRisk AssessmentRisk FactorsEpidemiologyGranulomatosis with polyangiitisVasculitis

Identifiers

PMID41475838
PMCPMC12766798

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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.