Evidence map›Paper›PMID 41136440›Full record

ArticleScientific reports2025

Analytical and clinical comparison of four SLE-associated autoantibodies in different autoimmune diseases.

Jing Yang, Lin Zhao, Shuiqing He, Mingxi Xu, Yu Liu, Xiaodan Kong

Abstract readComparative Study
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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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

4 citing papers in PubMed.

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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

6 authors.

Jing Yang *Department of Rheumatology, The Second Affiliated Hospital of Dalian Medical University, Dalian, China.
Lin Zhao *Department of Rheumatology, The Second Affiliated Hospital of Dalian Medical University, Dalian, China.
Shuiqing HeDepartment of Rheumatology, The Second Affiliated Hospital of Dalian Medical University, Dalian, China.
Mingxi XuDepartment of Rheumatology, The Second Affiliated Hospital of Dalian Medical University, Dalian, China.
Yu LiuDepartment of Rheumatology, The Second Affiliated Hospital of Dalian Medical University, Dalian, China. liuyu296545352@163.com.
Xiaodan KongDepartment of Rheumatology, The Second Affiliated Hospital of Dalian Medical University, Dalian, China. xiaodankong2008@sina.com.

Funding

1+x Program of Youth Medical clinical Technical Ability Improvement project 2024LCJSYL05
6 · The paper itself

Abstract

Autoantibodies associated with systemic lupus erythematosus (SLE) are often present in patients with a variety of autoimmune diseases, affecting the diagnosis and differentiation of the diseases. In this study, the positive rates and diagnostic efficiencies of anti-dsDNA, anti-nucleosome, anti-ribosomal P and anti-C1q antibodies were analysed in 216 SLE patients, 323 rheumatoid arthritis (RA) patients, 87 Sjogren's syndrome (SS) patients, 45 patients with other autoimmune diseases (OAD) and 52 healthy controls (HC). In addition to being high in SLE patients, the serum levels of anti-dsDNA and anti-nucleosome antibodies were also significantly higher in SS patients compared with OAD (P = 0.008, < 0.001). The ROC-AUCs for the four SLE-associated autoantibodies in distinguishing SLE patients from SS patients were lower than those in distinguishing SLE patients from HC. Therefore, SLE-associated autoantibody-positive SS patients represent a less studied and heterogeneous population, as these antibodies are also present in approximately 15% of all SS patients. Compared with SLE-associated autoantibody-negative SS patients, SS patients who were positive for SLE-associated autoantibodies were more likely to be positive for anti-nRNP/Sm autoantibodies (30.77% vs. 4.05%, P = 0.001). Oral ulcerations, rampant dental and pulmonary involvement were more frequent in SS patients who were positive for SLE-associated autoantibodies than in those who were negative for these autoantibodies (P = 0.018, 0.004 and < 0.001). In conclusion, SLE-associated autoantibody-positive SS patients represent a heterogeneous population, characterized by unique autoantibody profiles and clinical manifestations. This study may provide new insights for diagnostic refinement between SLE and SS patients.

Indexed as

AutoantibodiesAutoimmune DiseasesLupus Erythematosus, SystemicAdolescentAdultAgedAntibodies, AntinuclearArthritis, RheumatoidConnective Tissue DiseasesFemaleHumansMaleMiddle AgedNucleosomesRibosomesSjogren's SyndromeAntibodies, Antinuclearanti-dsDNA autoantibodyAnti-ribosomal P protein autoantibodiesAutoantibodiesNucleosomes

Identifiers

PMID41136440
PMCPMC12552497

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