Evidence map›Paper›PMID 42171924›Full record

Observational studyInternal and emergency medicine2026

The systemic immune-inflammation biomarkers in Sjögren's disease: associations with disease activity and extraglandular manifestations in a multicentric Italian cohort.

Stefano Stano, Venerito Vincenzo, Maria Giannotta, Fabio Cacciapaglia, Daniele Catamerò, Maria Iacovantuono, Paola Conigliaro, Benedetta Monosi, Daniele Domanico, Eduardo Urgesi and 4 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Internal and emergency medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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

1 citing paper in PubMed.

  1. Review
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

14 authors.

Stefano Stano *Rheumatology Unit - Department of Precision and Regenerative Medicine, Jonian Area (DiPReMeJ), University of Bari "Aldo Moro", Piazza G. Cesare 11, 70124, Bari, Italy.ORCID http://orcid.org/0000-0001-5207-7913
Venerito Vincenzo *Rheumatology Unit - Department of Precision and Regenerative Medicine, Jonian Area (DiPReMeJ), University of Bari "Aldo Moro", Piazza G. Cesare 11, 70124, Bari, Italy.ORCID http://orcid.org/0000-0002-2573-5930
Maria GiannottaRheumatology Unit - Department of Precision and Regenerative Medicine, Jonian Area (DiPReMeJ), University of Bari "Aldo Moro", Piazza G. Cesare 11, 70124, Bari, Italy.
Fabio CacciapagliaRheumatology Unit - Department of Precision and Regenerative Medicine, Jonian Area (DiPReMeJ), University of Bari "Aldo Moro", Piazza G. Cesare 11, 70124, Bari, Italy.
Daniele CatameròRheumatology Unit - Department of Precision and Regenerative Medicine, Jonian Area (DiPReMeJ), University of Bari "Aldo Moro", Piazza G. Cesare 11, 70124, Bari, Italy.
Maria IacovantuonoRheumatology, Allergology and Clinical Immunology, Department of Systems' Medicine, University of Rome Tor Vergata, Rome, Italy.ORCID http://orcid.org/0009-0002-4963-0663
Paola ConigliaroRheumatology, Allergology and Clinical Immunology, Department of Systems' Medicine, University of Rome Tor Vergata, Rome, Italy.ORCID http://orcid.org/0000-0001-7905-8413
Benedetta MonosiRheumatology, Allergology and Clinical Immunology, Department of Systems' Medicine, University of Rome Tor Vergata, Rome, Italy.
Daniele DomanicoRheumatology Unit - Department of Precision and Regenerative Medicine, Jonian Area (DiPReMeJ), University of Bari "Aldo Moro", Piazza G. Cesare 11, 70124, Bari, Italy.
Eduardo UrgesiUniversity Cardiologic Unit - Interdisciplinary Department of Medicine, Policlinico University Hospital, University of Bari "Aldo Moro", Bari, Italy.
Antonio VitaleDepartment of Medical Sciences, Surgery and Neurosciences, Research Center of Systemic Autoinflammatory Diseases and Behçet's Disease Clinic, University of Siena, Siena, Italy.
Maria Sole ChimentiRheumatology, Allergology and Clinical Immunology, Department of Systems' Medicine, University of Rome Tor Vergata, Rome, Italy.ORCID http://orcid.org/0000-0002-1343-1729
Florenzo Iannone *Rheumatology Unit - Department of Precision and Regenerative Medicine, Jonian Area (DiPReMeJ), University of Bari "Aldo Moro", Piazza G. Cesare 11, 70124, Bari, Italy.ORCID http://orcid.org/0000-0003-0474-5344
Giuseppe Lopalco *Rheumatology Unit - Department of Precision and Regenerative Medicine, Jonian Area (DiPReMeJ), University of Bari "Aldo Moro", Piazza G. Cesare 11, 70124, Bari, Italy. giuseppe.lopalco@uniba.it.ORCID http://orcid.org/0000-0003-4524-9566

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sjögren's disease (SjD) is an autoimmune exocrinopathy characterized by heterogeneous extraglandular manifestations (EGM). The systemic immune-inflammation biomarkers, including the neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and systemic immune-inflammation index (SII), have been proposed as indicators of the inflammatory burden, but data in SjD remain limited. This retrospective multicenter Italian study aimed to evaluate the NLR, PLR, and SII in exocrine SjD patients and across specific EGM. Consecutive patients fulfilling the 2016 ACR/EULAR classification criteria for SjD and with available full blood count data were included. Patients were classified as having exocrine or extraglandular SjD according to the presence of specific EGM. The NLR, PLR, and SII were calculated and compared across disease phenotypes and activity levels. Among 239 SjD patients (96% female, median age 59 years), 70% presented at least one EGM. Extraglandular SjD patients had longer disease duration (p = 0.04) and higher frequencies of hypergammaglobulinemia (p = 0.05), anti-nuclear antibodies (p = 0.0003), anti-SSA antibodies (p = 0.04), and rheumatoid factor (p = 0.04). Overall, the median NLR, PLR, and SII did not differ between exocrine and extraglandular SjD. However, patients with arthritis showed higher NLR (p = 0.02), PLR (p < 0.05), and SII (p = 0.005), while patients with interstitial lung disease displayed higher SII (p = 0.01). Extraglandular SjD patients with moderate-to-high disease activity showed increased NLR and SII (p = 0.004, for both). Systemic immune-inflammation biomarkers are inexpensive, readily available and easy to calculate. The NLR, PLR, and SII are associated with specific inflammatory phenotypes and higher disease activity in Italian SjD patients. Prospective studies are warranted to confirm these preliminary findings.

Indexed as

BiomarkersInflammationSjogren's SyndromeAdultAgedCohort StudiesFemaleHumansItalyLymphocytesMaleMiddle AgedNeutrophilsRetrospective StudiesBiomarkersDisease activityExtraglandular manifestationsSjögren’s diseaseSystemic immune-inflammation biomarkers

Identifiers

PMID42171924
PMCPMC13582351

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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.