ArticleScientific reports2026
Distinct molecular profile in Sjögren's syndrome is associated with disease activity and clinical manifestations.
Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- From immune activation to symptom burden: mechanisms and translational implications of immune-symptom uncoupling in Sjögren's disease.Frontiers in immunology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
14 authors.
Funding
Abstract
Sjögren's disease (SjD) is a systemic autoimmune condition for which reliable diagnostic and stratification biomarkers are still lacking. Several molecules have been implicated in its pathogenesis, and this study aimed to evaluate their potential as biomarkers in a monocentric cohort of SjD patients. Sera from 40 SjD patients (2016 ACR/EULAR criteria) and 41 matched controls were analyzed for 23 soluble inflammatory mediators using a Luminex® multiplex immunoassay. Clinical and laboratory correlations were examined, and multivariate logistic regression was performed. Compared with controls, SjD patients had significantly higher levels of IL-15 (11.52 ± 24.95 vs. 1.37 ± 1.26 pg/ml, P = 0.0009), monocyte chemoattractant protein (MCP)-1 (683.6 ± 1127 vs. 654.8 ± 608.9 pg/ml, P = 0.0203), TNFRII (8588 ± 2889 vs. 5505 ± 1007 pg/ml, P < 0.0001), and MMP-8 (6382 ± 12,697 vs. 6247 ± 6950 pg/ml, P = 0.0141), while IL-1RII was reduced (6267 ± 1699 vs. 8514 ± 2255 pg/ml, P < 0.0001). IL-15 correlated with hypergammaglobulinemia and monoclonal component, MCP-1 with focus score and sicca severity, and IL-1RII with anti-SSB positivity. Logistic regression identified TNFRII and IL-1RII as the strongest independent predictors of SjD (AUC = 0.89). This study supports the association of IL-15, TNFRII, and MCP-1 with immune dysregulation in SjD and highlights MMP-8 and IL-1RII as promising serological biomarkers. Validation in larger, longitudinal cohorts is warranted.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.