Evidence map›Paper›PMID 37558492›Full record

ArticleRMD open2023

Invasive fungal diseases in patients with autoimmune diseases: a case series from the French RESSIF network.

Simon Galmiche, Benjamin Thoreau, Stéphane Bretagne, Alexandre Alanio, André Paugam, Valérie Letscher-Bru, Sophie Cassaing, Jean-Pierre Gangneux, Hélène Guegan, Loïc Favennec and 25 more

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Article in RMD open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

10 citing papers in PubMed, 13 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

35 authors at 20 institutions in 3 countries.

Simon GalmicheEmerging Diseases Epidemiology Unit, Institut Pasteur, Université Paris Cité, Paris, Île-de-France, France simon.galmiche@pasteur.fr.ORCID 0000-0002-1691-1744
Benjamin ThoreauNational Referral Center for Rare Systemic Autoimmune Diseases, Department of Internal Medicine, Cochin Hospital, AP-HP, Université Paris Cité, Paris, Île-de-France, France.
Stéphane BretagneParasitologie - Mycologie, Hôpital St Louis, APHP, Paris, Île-de-France, France.
Alexandre AlanioParasitologie - Mycologie, Hôpital St Louis, APHP, Paris, Île-de-France, France.
André PaugamParasitologie - Mycologie, Université Paris Cité, Cochin Hospital, APHP, Paris, Île-de-France, France.
Valérie Letscher-BruLaboratoire de Parasitologie et Mycologie Médicale, Les Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Sophie CassaingParasitologie - Mycologie, Université de Toulouse, CHU Toulouse, Toulouse, Occitanie, France.
Jean-Pierre GangneuxUniversité de Rennes, CHU, INSERM, Irset: Institut de Recherche en Santé, Environnement et Travail, UMR_S 1085, Rennes, France.
Hélène GueganUniversité de Rennes, CHU, INSERM, Irset: Institut de Recherche en Santé, Environnement et Travail, UMR_S 1085, Rennes, France.
Loïc FavennecFrench National Cryptosporidiosis Reference Center, CHU de Rouen, Rouen, Normandie, France.
Alida MinozaFaculté de Médecine et Pharmacie, Université de Poitiers, Poitiers, Nouvelle-Aquitaine, France.
Florent MorioParasitologie - Mycologie, CHU Nantes, Nantes, Pays de la Loire, France.
Julie BonhommeMicrobiologie, CHU de Caen, ToxEMAC-ABTE Unicaen, Caen, Normandie, France.
Guillaume DesoubeauxCentre d'Étude des Pathologies Respiratoires - Inserm UMR1100, Université de Tours, Tours, France.
Odile EloyMicrobiologie, CH Versailles, Le Chesnay, Île-de-France, France.
Lilia HasseineParasitologie - Mycologie, hôpital de l'Archet, CHU Nice, Nice, Provence-Alpes-Côte d'Azur, France.
Milène SassoLaboratoire de Parasitologie - Mycologie, CHU Nîmes, Université de Montpellier, CNRS, IRD, MiVEGEC, Nimes, Occitanie, France.
Laurence MillonLaboratoire de Parasitologie - Mycologie, CHU de Besançon, Besançon, Bourgogne-Franche-Comté, France.
Anne-Pauline BellangerLaboratoire de Parasitologie - Mycologie, CHU de Besançon, Besançon, Bourgogne-Franche-Comté, France.
Philippe PoirierParasitologie - Mycologie, CHU Clermont-Ferrand, Clermont-Ferrand, France.
Maxime MoniotParasitologie - Mycologie, CHU Clermont-Ferrand, Clermont-Ferrand, France.
Taieb ChouakiMycologie - parasitologie, CHU Amiens-Picardie, Amiens, Hauts-de-France, France.
Antoine HugueninParasitologie - Mycologie, hôpital Maison-Blanche, CHU de Reims, Reims, France.
Frédéric DalleParasitologie - Mycologie, Plateforme de Biologie Hospitalo-Universitaire Gérard Mack, Dijon, Bourgogne-Franche-Comté, France.
Bernard BouteilleParasitologie - Mycologie, Centre de Biologie et de Recherche en Santé, CHU Limoges, Limoges, Nouvelle-Aquitaine, France.
Muriel NicolasMycologie - Parasitologie, Centre Hospitalier Universitaire Pointe-à-Pitre Abymes, Pointe-à-Pitre, Guadeloupe.
Nicole Desbois-NogardParasitologie - Mycologie, CHU de Martinique, Fort-de-France, Martinique.
Marie-Elisabeth BougnouxLaboratoire de Parasitologie - Mycologie, Service de Microbiologie, Necker-Enfants Malades University Hospital, APHP, Paris, Île-de-France, France.
François DanionMaladies infectieuses et tropicales, Les Hôpitaux Universitaires de Strasbourg, Strasbourg, Grand Est, France.
Vincent PoindronService d'Immunologie clinique, Hopitaux universitaires de Strasbourg, Strasbourg, France.
Antoine NéelCRTI UMR 1064, INSERM, Université de Nantes, Nantes, France.
Karine Boukris-SitbonInstitut Pasteur, Université Paris Cité, CNRS, National Reference Center for Invasive Mycoses and Antifungals, Translational Mycology Research Group, Mycology Department, Paris, Île-de-France, France.
Fanny LanternierInstitut Pasteur, Université Paris Cité, CNRS, National Reference Center for Invasive Mycoses and Antifungals, Translational Mycology Research Group, Mycology Department, Paris, Île-de-France, France.
Benjamin TerrierNational Referral Center for Rare Systemic Autoimmune Diseases, Department of Internal Medicine, Cochin Hospital, AP-HP, Université Paris Cité, Paris, Île-de-France, France.ORCID 0000-0001-6612-7336
French Mycoses Study Group
Centre National de la Recherche Scientifique · FRInserm · FRDélégation Paris 5 · FRHôpitaux Universitaires de Strasbourg · FRCentre Hospitalier de Versailles · FRCentre Hospitalier Universitaire Amiens-Picardie · FRCentre Hospitalier Universitaire de Besançon · FRCentre Hospitalier Universitaire de Caen Normandie · FRCentre Hospitalier Universitaire de Clermont-Ferrand · FRCentre Hospitalier Universitaire de Limoges · FRCentre Hospitalier Universitaire de Martinique · MQCentre Hospitalier Universitaire de Nantes · FRCentre Hospitalier Universitaire de Reims · FRCentre Hospitalier Universitaire de Rouen · FRCentre Hospitalier Universitaire Pointe-à-Pitre · GPHôpital Necker-Enfants Malades · FRInstitut de Chimie de Nice · FRInstitut Pasteur · FRProcédés Alimentaires et Microbiologiques · FRUniversité de Poitiers · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesWe aimed to describe patients with autoimmune diseases (AID) developing invasive fungal disease (IFD) and identify factors associated with short-term mortality.

methodsWe analysed cases of IFD associated with AID from the surveillance network of invasive fungal diseases (Réseau de surveillance des infections fongiques invasives, RESSIF) registry of the French national reference centre for invasive mycoses. We studied association of AID-specific treatments with 30-day mortality. We analysed total lymphocyte and CD4-T cell counts in patients with

resultsFrom 2012 to 2018, 549 individuals with IFD and AID were included, mainly with PCP (n=227, 41.3%), fungemia (n=167, 30.4%) and invasive aspergillosis (n=84, 15.5%). Rheumatoid arthritis (RA) and anti-neutrophil cytoplasmic antibodies (ANCA)-associated vasculitides (AAV) were the most frequent AID in PCP (n=55 and 25, respectively) and invasive aspergillosis (n=15 and 10, respectively), inflammatory bowel diseases (IBDs) were predominant in fungemia (n=36). At IFD diagnosis, 365 (66.5%) patients received glucocorticoids (GCs), 285 (51.9%) immunosuppressants, 42 (7.7%) tumor necrosis factor (TNF)-α blockers, 75 (13.7%) other biologics. Mortality at 30 days was 28.1% (143/508). Fungemia and high-dose GCs were independently associated with higher 30-day mortality. In PCP patients, lymphopenia <1500/mm

conclusionIFD associated with AID occurs primarily in RA, AAV and IBD, especially when treated with GCs and immunosuppressants. Mortality is high, especially for patients on high-dose GCs. Lymphopenia may help identify risk of PCP, but normal CD4+T cell count does not rule out the risk. Further studies are needed to assess the individual risk factors for IFD.

Indexed as

Autoimmune DiseasesInvasive Fungal InfectionsAgedFemaleFranceGlucocorticoidsHumansImmunosuppressive AgentsMaleMiddle AgedPrevalenceRisk FactorsGlucocorticoidsImmunosuppressive AgentsAntirheumatic AgentsArthritis, RheumatoidAutoimmune DiseasesGlucocorticoids

Identifiers

PMID37558492
PMCPMC10414070
OpenAlexW4385715653

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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.