Evidence map›Paper›PMID 35926375›Full record

Observational studyJournal of autoimmunity2022

COVID-19 outcomes in giant cell arteritis and polymyalgia rheumatica versus rheumatoid arthritis: A national, multicenter, cohort study.

Matheus Vieira, Cloé Comarmond, Julien Labreuche, Adrien Mirouse, David Saadoun, Christophe Richez, René-Marc Flipo, Eric Hachulla, Elodie Drumez, Patrice Cacoub and 1 more

Registry-linked trialAbstract readObservational StudyMulticenter Study
In one paragraph

Observational study in Journal of autoimmunity, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04353609 (Covid-19 in Patients With Chronic Inflammatory Rheumatism, Auto-immune or Auto-inflammatory Rare and Non-rare Diseases), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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.

NCT04353609 completednot on this map

Covid-19 in Patients With Chronic Inflammatory Rheumatism, Auto-immune or Auto-inflammatory Rare and Non-rare Diseases : a Retrospective Multicenter Observational Study

TypeobservationalSponsorUniversity Hospital, LilleRan2020 to 2020Enrolled13,770ConditionsSars-CoV2, Chronic Inflammatory Rheumatism, Autoimmune Diseases
3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
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.

Matheus VieiraSorbonne Universités AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Département de Médecine Interne et Immunologie Clinique, F-75013, Paris, France; Centre National de Références Maladies Autoimmunes Systémiques Rares, Centre National de Références Maladies Autoinflammatoires et Amylose Inflammatoire, France; Inflammation-Immunopathology-Biotherapy Department (DMU 3iD), France; INSERM 959, Groupe Hospitalier, AP-HP, Paris, France.
Cloé ComarmondHôpital Lariboisière, Département de Médecine Interne et Immunologie, Clinique, Université, Paris, Cité, France.
Julien LabreucheUniv. Lille, CHU Lille, ULR 2694 - METRICS: Évaluation des technologies de Santé et des Pratiques Médicales, F-59000, Lille, France; CHU Lille, Department of Biostatistics, F-59000, Lille, France.
Adrien MirouseSorbonne Universités AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Département de Médecine Interne et Immunologie Clinique, F-75013, Paris, France; Centre National de Références Maladies Autoimmunes Systémiques Rares, Centre National de Références Maladies Autoinflammatoires et Amylose Inflammatoire, France; Inflammation-Immunopathology-Biotherapy Department (DMU 3iD), France; INSERM 959, Groupe Hospitalier, AP-HP, Paris, France.
David SaadounSorbonne Universités AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Département de Médecine Interne et Immunologie Clinique, F-75013, Paris, France; Centre National de Références Maladies Autoimmunes Systémiques Rares, Centre National de Références Maladies Autoinflammatoires et Amylose Inflammatoire, France; Inflammation-Immunopathology-Biotherapy Department (DMU 3iD), France; INSERM 959, Groupe Hospitalier, AP-HP, Paris, France.
Christophe RichezService de Rhumatologie, Centre de Référence des Maladies Autoimmunes Systémiques Rares de L'Est et Du Sud-Ouest de France, CHU de Bordeaux and UMR-CNRS 5164, Université de Bordeaux, Bordeaux, France.
René-Marc FlipoService de Rhumatologie, Université Lille, CHU Lille, Lille, France.
Eric HachullaUniversity Lille, INSERM U995, CHU Lille, Service de Médecine Interne et Immunologie Clinique, Centre de Référence des Maladies Autoimmunes Systémiques rares Du Nord et Nord-Ouest de France (CeRAINO), U1286 - INFINITE - Institute for Translational Research in Inflammation, 59000, Lille, France.
Elodie DrumezUniv. Lille, CHU Lille, ULR 2694 - METRICS: Évaluation des technologies de Santé et des Pratiques Médicales, F-59000, Lille, France; CHU Lille, Department of Biostatistics, F-59000, Lille, France.
Patrice CacoubSorbonne Universités AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Département de Médecine Interne et Immunologie Clinique, F-75013, Paris, France; Centre National de Références Maladies Autoimmunes Systémiques Rares, Centre National de Références Maladies Autoinflammatoires et Amylose Inflammatoire, France; Inflammation-Immunopathology-Biotherapy Department (DMU 3iD), France; INSERM 959, Groupe Hospitalier, AP-HP, Paris, France. Electronic address: patrice.cacoub@aphp.fr.
FAIR/SFR/SNFMI/SOFREMIP/CRI/IMIDIATE consortium and contributors

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo determine whether giant cell arteritis and polymyalgia rheumatica (GCA/PMR) represent independent risk factors for worse outcomes in COVID-19.

methodsObservational, national, French, multicenter cohort (NCT04353609) comprising patients aged ≥18 years with confirmed diagnoses of either GCA, PMR or rheumatoid arthritis (RA) having presented COVID-19; those under rituximab were excluded. Primary endpoint was COVID-19 severity in GCA/PMR patients as compared to RA. We also aimed to describe the evolution of GCA/PMR patients following COVID-19. Multinomial logistic regression models were performed, with and without adjustment on pre-specified confounding factors (i.e., age, sex, body mass index, arterial hypertension, diabetes and cardiovascular disease). Unadjusted and adjusted multinomial odds-ratio (OR/aOR) and their 95% confidence intervals (CIs) were calculated as effect size using RA as reference group.

resultsBetween April 15, 2020, and August 20, 2021, 674 patients [45 (6.6%) GCA, 47 (7.0%) PMR, 582 (86.4%) RA; 62.8 years, 73.2% female] were included. Compared to RA patients, those with GCA/PMR were older and more frequently presented hypertension, diabetes and cardiovascular disease. Severe COVID-19 and death occurred in 24 (26.1%) and 16 (17.8%) patients with GCA/PMR, respectively. Unadjusted analyses revealed higher odds of severe COVID-19 [OR = 3.32 (95% CI 1.89-5.83; p < 0.001)] and death [OR = 3.20 (95%CI 1.67-6.13; p < 0.001)] for GCA/PMR compared to RA. After model adjustment, these odds were attenuated.

conclusionPatients with GCA/PMR were more likely to have severe COVID-19 and higher mortality compared to those with RA. This worse prognosis is mostly due to well known risk factors for the general population rather than vasculitis per se.

Indexed as

Arthritis, RheumatoidCardiovascular DiseasesCOVID-19Giant Cell ArteritisHypertensionPolymyalgia RheumaticaAdolescentAdultCohort StudiesFemaleHumansMaleCOVID-19Giant cell arteritisPolymyalgia rheumaticaRheumatoid arthritisSARS-CoV-2

Identifiers

PMID35926375
PMCPMC9296684

What OpenQuestion holds

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Registered trials

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.