Evidence map›Paper›PMID 35041109›Full record

ArticleClinical rheumatology2022

Clinical phenotype and cytokine profile of adult IgA vasculitis with joint involvement.

Alice Delapierre, Benjamin Terrier, Evangéline Pillebout, Pauline Baudart, Noémie Jourde-Chiche, Bertrand Lioger, Nihal Martis, Guillaume Moulis, Etienne Rivière, Noémie Le Gouellec and 14 more

Abstract read
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In one paragraph

Article in Clinical rheumatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
5.2field-weighted citation impact, top 3% 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

8 citing papers in PubMed, 26 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

24 authors at 14 institutions in 1 country.

Alice DelapierreDepartment of Rheumatology, Normandie UNIV, UNICAEN, CHU de Caen Normandie, 14 000, Caen, France.
Benjamin TerrierUniversité Paris Descartes, Paris, France.
Evangéline PilleboutDepartment of Nephrology, Hôpital Saint-Louis, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
Pauline BaudartDepartment of Rheumatology, Normandie UNIV, UNICAEN, CHU de Caen Normandie, 14 000, Caen, France.
Noémie Jourde-ChicheAix-Marseille Univ, C2VN, INSERM, INRA, Centre de Néphrologie Et Transplantation Rénale, CHU de La Conception, AP-HM, Marseille, France.
Bertrand LiogerDepartment of Internal Medicine, Hôpital Saint Louis, APHP, Paris, France.
Nihal MartisDepartment of Internal Medicine, CHU, Nice, France.
Guillaume MoulisDepartment of Internal Medicine, CHU, Toulouse, France.
Etienne RivièreDepartment of Internal Medicine, CHU, Bordeaux, France.
Noémie Le GouellecDepartment of Internal Medicine and Nephrology, Valenciennes, CH, France.
Loïc RaffrayDepartment of Internal Medicine, CHU, La Réunion, France.
Geoffrey UrbanskiDepartment of Internal Medicine, CHU, Angers, France.
Sébastien SangesDépartement de Médecine Interne Et Immunologie Clinique, CHU Lille, 59000, Lille, France.
Francois MaurierDepartment of Internal Medicine, Hôpitaux privés, Metz, France.
Alban DerouxDepartment of Internal Medicine, CHU de Grenoble, Grenoble, France.
Arsène MekinianDepartment of Internal Medicine, Hôpital Saint-Antoine, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
Renato MonteiroCenter of Research On Inflammation INSERM U1149, CNRS ERL8252, Paris Diderot University, Paris, France.
Christian MarcelliDepartment of Rheumatology, Normandie UNIV, UNICAEN, CHU de Caen Normandie, 14 000, Caen, France.
Loïc GuillevinUniversité Paris Descartes, Paris, France.
Francois MaillotDepartment of Internal Medicine and Clinical Immunology, CHRU Tours, Tours, France.
Bruno LucasParis Descartes University, Cochin Institute, CNRS UMR8104, INSERM U1016, Paris, France.
Achille AoubaDepartment of Internal Medicine and Clinical Immunology, Normandie Univ, UNICAEN, CHU de Caen Normandie, 14000, Caen, France.
Alexandra Audemard-VergerDepartment of Internal Medicine and Clinical Immunology, CHRU Tours, Tours, France. alexandra.audemardverger@univ-tours.fr.ORCID http://orcid.org/0000-0002-0226-5016
French Vasculitis Study Group (FVSG) and the HSPrognosis group
Centre Hospitalier Universitaire de Caen Normandie · FRAssistance Publique – Hôpitaux de Paris · FRCentre National de la Recherche Scientifique · FRDélégation Paris 5 · FRInserm · FRUniversité de Tours · FRCentre Hospitalier de Valenciennes · FRCentre Hospitalier Universitaire d'Angers · FRCentre Hospitalier Universitaire de Bordeaux · FRCentre Hospitalier Universitaire de Grenoble · FRCentre Hospitalier Universitaire de La Réunion · FRCentre Hospitalier Universitaire de Nice · FRNormandie Université · FRSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveJoint involvement can be observed during the course of adult IgA vasculitis (IgAV). However, clinical picture, prognosis, or pathophysiological data associated with this condition have been overlooked. We aimed to describe the clinical characteristics and outcome of IgAV patients with joint involvement and look to a specific cytokine profile.

methodsWe analyzed clinical and biological data from a nationwide study that included adult IgAV patients. Presentation and outcomes of patients with or without joint involvement were compared at baseline and during follow-up. Plasma cytokine measurements of IgAV patients included in a prospective study were also analyzed using multiplex assays.

resultsAmong 260 patients, 62% had joint involvement. Among them, rheumatological manifestations included arthralgia (100%) or arthritis (16%), mostly involving the knees and ankles. In multivariate analysis, patients with joint involvement, compared to those without, were younger (p = 0.002; OR 0.87; 95% CI 0.80-0.95) and showed more frequent gastrointestinal tract involvement (p = 0.012; OR = 2.08; 95% CI 1.18-3.67). However, no difference in terms of clinical response, relapse, end-stage renal disease, or death was observed between groups. Among 13 cytokines measured, plasma interleukin (IL)-1β level was higher in patients with joint involvement compared to those without (mean ± SEM IL-1β, 3.5 ± 1.2 vs. 0.47 ± 0.1 pg/ml; p = 0.024) or healthy controls (vs. 1.2 ± 0.5 pg/ml; p = 0.076).

conclusionJoint involvement is frequent in adult IgAV and is associated with more frequent gastrointestinal involvement. Increased plasma IL-1β levels raise the question of targeting this cytokine in patients with chronic and/or refractory joint involvement. Key Points • Joint involvement in adult IgAV is a frequent manifestation. • Joint involvement is associated with more frequent gastrointestinal manifestations. • Interleukin-1β (IL-1β) might orchestrate joint inflammation in adult IgAV. • IL-1β might be a therapeutic target in patients with chronic and/or refractory joint involvement.

Indexed as

IgA VasculitisCytokinesHumansImmunoglobulin APhenotypeProspective StudiesCytokinesImmunoglobulin AGastrointestinal tract involvementHenoch-Schönlein purpuraIgA vasculitisIL-1βJoint involvement

Identifiers

PMID35041109
OpenAlexW4206433787

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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.