Evidence map›Paper›PMID 35896805›Full record

ArticleRheumatology international2023

The diagnostic challenge of patients with anti-U1-RNP antibodies.

Ines Elhani, Kathy Khoy, Delphine Mariotte, Elisabeth Comby, Christian Marcelli, Brigitte Le Mauff, Alexandra Audemard-Verger, Jonathan Boutemy, Gwénola Maigné, Nicolas Martin Silva and 2 more

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Article in Rheumatology international, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 17 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

12 authors at 5 institutions in 1 country.

Ines ElhaniDepartment of Internal Medicine, Caen University Hospital, Caen, France.ORCID http://orcid.org/0000-0002-9767-2262
Kathy KhoyLaboratory of Immunology, Department of Biology, Caen University Hospital, Caen, France.ORCID http://orcid.org/0000-0002-7021-1415
Delphine MariotteLaboratory of Immunology, Department of Biology, Caen University Hospital, Caen, France.ORCID http://orcid.org/0000-0002-9989-4272
Elisabeth CombyLaboratory of Immunology, Department of Biology, Caen University Hospital, Caen, France.
Christian MarcelliDepartment of Rheumatology, Caen University Hospital, Caen, France.ORCID http://orcid.org/0000-0002-9699-2467
Brigitte Le MauffLaboratory of Immunology, Department of Biology, Caen University Hospital, Caen, France.ORCID http://orcid.org/0000-0001-9242-4895
Alexandra Audemard-VergerDepartment of Internal Medicine and Clinical Immunology, CHRU Tours, Tours, France.ORCID http://orcid.org/0000-0002-0226-5016
Jonathan BoutemyDepartment of Internal Medicine, Caen University Hospital, Caen, France.
Gwénola MaignéDepartment of Internal Medicine, Caen University Hospital, Caen, France.ORCID http://orcid.org/0000-0002-3023-361X
Nicolas Martin SilvaDepartment of Internal Medicine, Caen University Hospital, Caen, France.ORCID http://orcid.org/0000-0002-1536-1373
Achille AoubaDepartment of Internal Medicine, Caen University Hospital, Caen, France.ORCID http://orcid.org/0000-0003-1726-3811
Hubert de BoyssonDepartment of Internal Medicine, Caen University Hospital, Caen, France. deboysson-h@chu-caen.fr.ORCID http://orcid.org/0000-0001-9083-8365
Centre Hospitalier Universitaire de Nice · FRUniversité de Caen Normandie · FRInserm · FRNormandie Université · FRUniversité de Tours · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anti-U1-RNP antibodies are necessary for the diagnosis of mixed connective tissue disease (MCTD), but they are also prevalent in other connective tissue diseases, especially systemic lupus erythematosus (SLE), from which distinction remains challenging. We aimed to describe the presentation and outcome of patients with anti-U1-RNP antibodies and to identify factors to distinguish MCTD from SLE. We retrospectively applied the criteria sets for MCTD, SLE, systemic sclerosis (SSc) and rheumatoid arthritis (RA) to all patients displaying anti-U1-RNP antibodies in the hospital of Caen from 2000 to 2020. Thirty-six patients were included in the analysis. Eighteen patients (50%) satisfied at least one of the MCTD classifications, 11 of whom (61%) also met 2019 ACR/EULAR criteria for SLE. Twelve other patients only met SLE without MCTD criteria, and a total of 23 patients (64%) met SLE criteria. The most frequent manifestations included Raynaud's phenomenon (RP, 91%) and arthralgia (67%). We compared the characteristics of patients meeting only the MCTD (n = 7), SLE (n = 12), or both (n = 11) criteria. Patients meeting the MCTD criteria were more likely to display SSc features, including sclerodactyly (p < 0.01), swollen hands (p < 0.01), RP (p = 0.04) and esophageal reflux (p < 0.01). The presence of scleroderma features (swollen hands, sclerodactyly, gastro-oesophageal reflux), was significantly associated with the diagnosis of MCTD. Conversely, the absence of those manifestations suggested the diagnosis of another definite connective tissue disease, especially SLE.

Indexed as

Gastroesophageal RefluxLupus Erythematosus, SystemicMixed Connective Tissue DiseaseScleroderma, LocalizedScleroderma, SystemicAntibodies, AntinuclearHumansRetrospective StudiesAntibodies, AntinuclearAnti-U1-RNP antibodiesConnective tissue diseaseMixed connective tissue diseaseSystemic lupus erythematosus

Identifiers

PMID35896805
OpenAlexW4288058196

What OpenQuestion holds

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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.