Evidence map›Paper›PMID 34207757›Full record

ArticleDiagnostics (Basel, Switzerland)2021

Quantification of Antifibrillarin (anti-U3 RNP) Antibodies: A New Insight for Patients with Systemic Sclerosis.

Audrey Benyamine, Daniel Bertin, Noémie Resseguier, Xavier Heim, Julien Bermudez, David Launay, Sylvain Dubucquoi, Adrian Hij, Dominique Farge, Alain Lescoat and 8 more

Open access · goldAbstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Review
  3. Biomarkers in Systemic Sclerosis: An Overview.Current issues in molecular biology · 2023
    Review
  4. Advanced Autoantibody Testing in Systemic Sclerosis.Diagnostics (Basel, Switzerland) · 2023
    Review
  5. Article
  6. Fibrillarin antibodies in systemic sclerosis.Archives of rheumatology · 2022
    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

18 authors at 6 institutions in 2 countries.

Audrey BenyamineInternal Medicine Department, North Hospital of Marseilles, Public Assistance Hospital of Marseilles (AP-HM), 13015 Marseilles, France.
Daniel BertinImmunology Laboratory, La Conception Hospital, Public Assistance Hospital of Marseilles (AP-HM), 13005 Marseilles, France.
Noémie ResseguierEpidemiology and Health Economics, La Timone Hospital, AP-HM, Aix Marseilles University (AMU), 13005 Marseilles, France.ORCID 0000-0003-0816-4053
Xavier HeimAix Marseilles University (AMU), INSERM, INRA, C2VN, 13005 Marseilles, France.ORCID 0000-0002-9459-4318
Julien BermudezAix Marseilles University (AMU), INSERM, INRA, C2VN, 13005 Marseilles, France.ORCID 0000-0001-8823-0959
David LaunayUniv. Lille, U1286-INFINITE-Institute for Translational Research in Inflammation, F-59000 Lille, France.
Sylvain DubucquoiImmunology Institute, Hospital University Center of Lille, 59037 Lille, France.
Adrian HijPublic Assistance Hospital of Paris, Saint-Louis Hospital, Autoimmune and Vascular Disease Unit, Internal Medicine (UF04), Center of reference for rare systemic autoimmune diseases (FAI2R), Université de Paris, EA 3518, Paris, France.
Dominique FargePublic Assistance Hospital of Paris, Saint-Louis Hospital, Autoimmune and Vascular Disease Unit, Internal Medicine (UF04), Center of reference for rare systemic autoimmune diseases (FAI2R), Université de Paris, EA 3518, Paris, France.
Alain LescoatInternal Medicine and Clinical Immunology Department, Hospital University Center of Rennes, 35000 Rennes, France.
Isabelle Bahon-RiedingerImmunology Laboratory, Hospital University Center of Rennes, 35033 Rennes, France.
Nouria BenmostefaInternal Medicine Department, Center of reference for rare systemic autoimmune diseases of Ile de France, Cochin Hospital, Public Assistance Hospital of Paris (AP-HP), 75014 Paris, France.
Luc MouthonInternal Medicine Department, Center of reference for rare systemic autoimmune diseases of Ile de France, Cochin Hospital, Public Assistance Hospital of Paris (AP-HP), 75014 Paris, France.
Jean-Robert HarléInternal Medicine Department, La Timone Hospital, Public Assistance Hospital of Marseilles (AP-HM), 13005 Marseilles, France.
Gilles KaplanskiAix Marseilles University (AMU), INSERM, INRA, C2VN, 13005 Marseilles, France.
Pascal RossiInternal Medicine Department, North Hospital of Marseilles, Public Assistance Hospital of Marseilles (AP-HM), 13015 Marseilles, France.
Nathalie BardinAix Marseilles University (AMU), INSERM, INRA, C2VN, 13005 Marseilles, France.
Brigitte GranelInternal Medicine Department, North Hospital of Marseilles, Public Assistance Hospital of Marseilles (AP-HM), 13015 Marseilles, France.ORCID 0000-0001-7995-8817
Inserm · FRHôpital Cochin · FRUniversité Paris Cité · FRAix-Marseille Université · FRAssistance Publique Hôpitaux de Marseille · FRUniversité de Rennes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe detection of additional autoantibodies is of great concern in systemic sclerosis (SSc) when those included in the ACR/EULAR classification are negative. In this context, the interest of antifibrillarin (anti-U3RNP) autoantibodies (AFAs) in the routine evaluation of SSc remains unclear. We aimed to assess the relevance of AFAs and their clinical association in SSc patients.

methodsIn a multicenter observational retrospective study, we collected immunological and clinical data associated with AFA positivity in SSc (

resultsWe confirmed a typical nuclear IIF pattern and showed that AFAs are mostly exclusive towards SSc conventional autoantibodies. Although also observed in non-SSc patients, high levels of AFAs with the ELiA technique allowed the diagnosis of SSc. Compared to AFA-negative SSc patients, AFA-positive SSc patients more frequently exhibited visceral involvements. They more frequently suffered from the diffuse cutaneous form and had a higher global severity of the disease.

conclusionsWe demonstrate the usefulness of quantifying AFAs in the immunological exploration of SSc, especially when patients are seronegative for SSc conventional autoantibodies and display a typical IIF pattern. AFAs might constitute an interesting marker of SSc severity.

Indexed as

antifibrillarin antibodiesanti-U3 RNP antibodiesautoantibodiessystemic sclerosis

Identifiers

PMID34207757
PMCPMC8226926
OpenAlexW3170687176

What OpenQuestion holds

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LicenceCC BY
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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.