Evidence map›Paper›PMID 32616563›Full record

ArticleLupus science & medicine2020

Systemic lupus erythematosus and neutropaenia: a hallmark of haematological manifestations.

Aurore Meyer, Aurélien Guffroy, Gilles Blaison, Yannick Dieudonne, Zahir Amoura, Bernard Bonnotte, Christoph Fiehn, Pierre Kieffer, Hannes Martin Lorenz, Nadine Magy-Bertrand and 10 more

Open access · goldAbstract read
In one paragraph

Article in Lupus science & medicine, 2020. 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
1.9field-weighted citation impact, top 13% 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, 17 citations in OpenAlex.

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

20 authors at 13 institutions in 2 countries.

Aurore MeyerDepartment of Clinical Immunology and Internal Medicine, National Reference Center for autoimmune diseases (RESO), Strasbourg University Hospital, Strasbourg, France.
Aurélien GuffroyDepartment of Clinical Immunology and Internal Medicine, National Reference Center for autoimmune diseases (RESO), Strasbourg University Hospital, Strasbourg, France aurelien.guffroy@chru-strasbourg.fr.ORCID 0000-0003-0615-5305
Gilles BlaisonDepartment of Internal Medicine, Hôpitaux Civils de Colmar, Colmar, Alsace, France.
Yannick DieudonneDepartment of Clinical Immunology and Internal Medicine, National Reference Center for autoimmune diseases (RESO), Strasbourg University Hospital, Strasbourg, France.
Zahir AmouraDepartment of Internal Medicine, Institut E3M, Assistance Publique Hôpitaux de Paris (APHP), Groupement Hospitalier Pitié Salpêtrière, Paris, France.
Bernard BonnotteDepartment of Clinical Immunology and Internal Medicine, CHU Dijon Bourgogne, Dijon, France.
Christoph FiehnACURA Centre for Rheumatic Diseases, Baden-Baden, Germany.
Pierre KiefferDepartment of Internal Medicine, Centre hospitalier de Mulhouse, Mulhouse, France.
Hannes Martin LorenzDepartment of Medicine V, University Hospital Heidelberg, Center for Rheumatic Diseases Baden-Baden, Heidelberg, Germany.
Nadine Magy-BertrandDepartment of Internal Medicine, CHU de Besançon, Besançon, France.
François MaurierDepartment of Internal Medicine, Hôpitaux Privés de Metz, Metz, France.
Jean-Louis PennaforteDepartment of Internal Medicine, CHU de Reims, Hôpital Robert Debré, Reims, France.
Hans-Hartmut PeterDepartment of Rheumatology and Clinical Immunology, Medical Center - Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Andreas SchwartingDepartment of Internal Medicine, Universitätsmedizin, Mainz, Germany.
Jean SibiliaDepartment of Rheumatology, National Reference Center for autoimmune diseases (RESO), Hôpitaux universitaires de Strasbourg, Strasbourg, France.
Laurent ArnaudUFR Médecine, Université de Strasbourg, Strasbourg, France.ORCID 0000-0002-8077-8394
Thierry MartinDepartment of Clinical Immunology and Internal Medicine, National Reference Center for autoimmune diseases (RESO), Strasbourg University Hospital, Strasbourg, France.
Reinhard Edmund VollDepartment of Rheumatology and Clinical Immunology, Medical Center - Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Anne-Sophie KorganowDepartment of Clinical Immunology and Internal Medicine, National Reference Center for autoimmune diseases (RESO), Strasbourg University Hospital, Strasbourg, France.
LBBR/Rarenet group
Inserm · FRUniversity of Freiburg · DEAcura Kliniken · DEAssistance Publique – Hôpitaux de Paris · FRCentre Hospitalier de Mulhouse · FRCentre Hospitalier Universitaire de Besançon · FRCentre Hospitalier Universitaire de Reims · FRCHU Dijon Bourgogne · FRHeidelberg University · DEHopitaux Civils de Colmar · FRHôpitaux Universitaires de Strasbourg · FRJohannes Gutenberg University Mainz · DEUniversité de Strasbourg · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveSystemic lupus is a chronic autoimmune disease characterised by its phenotypic heterogeneity. Neutropaenia is a frequent event in SLE occurring in 20%-40% of patients depending on the threshold value of neutrophil count. On a daily basis, the management of neutropaenia in SLE is difficult with several possible causes. Moreover, the infectious consequences of neutropaenia in SLE remain not well defined.

methods998 patients from the Lupus BioBank of the upper Rhein (LBBR), a large German and French cohort of patients with SLE, mostly of Caucasian origin (83%), were included in this study. Neutropaenia was considered when neutrophil count was below 1800×10

results208 patients with neutropaenia (21%) were compared with 779 SLE patients without neutropaenia. Neutropaenia in SLE was significantly associated with thrombocytopaenia (OR 4.11 (2.57-10.3)), lymphopaenia (OR 4.41 (2.51-11.5)) and low C3 (OR 1.91 (1.03-4.37)) in multivariate analysis. 65 representative patients with neutropaenia were analysed. Neutropaenia was moderate to severe in 38%, chronic in 31%, and both severe and chronic in 23% of cases. Moderate to severe and chronic neutropaenia were both associated with lymphopaenia and thrombopaenia. Chronic neutropaenia was also associated anti-Ro/SSA antibodies and moderate to severe neutropaenia with oral ulcers.

conclusionThis study is to date the largest cohort to describe neutropaenia in SLE. Neutropaenia displays a strong association with other cytopaenias, suggesting a common mechanism. Chronic neutropaenia is associated with anti-Ro/SSA antibodies with or without identified Sjögren's disease.

Indexed as

AdultAntibodies, AntinuclearAutoimmune DiseasesCase-Control StudiesComplement C3Cross-Sectional StudiesFemaleFranceGermanyHumansLupus Erythematosus, SystemicLymphopeniaMaleNeutropeniaSjogren's SyndromeThrombocytopeniaAntibodies, AntinuclearComplement C3SS-A antibodiesautoantibodiesautoimmune diseaseslupus erythematosus, systemic

Identifiers

PMID32616563
PMCPMC7333801
OpenAlexW3040155617

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.