Evidence map›Paper›PMID 42835207›Full record

ArticleFrontiers in immunology2026

The obesity paradox in primary Sjögren's disease: immunometabolic associations of chemerin, platelet count, and statin use.

Kincső Mezei, Viktória Orosz, Ildikó Fanny Horváth, Zsófia Aradi, Hajnalka Lőrincz, Mariann Harangi, Antónia Szántó

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Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Kincső MezeiDivision of Clinical Immunology, Institute of Internal Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Viktória OroszDivision of Clinical Immunology, Institute of Internal Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Ildikó Fanny HorváthDivision of Clinical Immunology, Institute of Internal Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Zsófia AradiDivision of Clinical Immunology, Institute of Internal Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Hajnalka LőrinczDivision of Metabolism, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Mariann HarangiDivision of Metabolism, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Antónia SzántóDivision of Clinical Immunology, Institute of Internal Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Sjögren's disease is characterized by autoimmune destruction of exocrine glands. Obesity generally worsens the course of many diseases; however, earlier observations in our cohort suggested a paradoxically lower disease activity (ESSDAI) in overweight/obese patients. This cross-sectional study aimed to investigate potential mechanisms underlying these findings. Methods: Chemerin and oxidized low-density lipoprotein (oxLDL) levels were measured in a subset of regularly followed patients (n=75). Patients were stratified by body mass index (BMI): BMI <25 kg/m² ("non-obese", n=27) and BMI ≥25 kg/m² ("overweight/obese", n=48). Demographic, laboratory, and immunological parameters, disease activity (ESSDAI), extraglandular manifestations, and treatments were compared using biostatistical analyses. Results: Chemerin and oxLDL levels did not differ significantly between groups. ESSDAI was significantly lower in overweight/obese patients (5.04 vs. 2.76; p=0.04), while complement c3 levels were higher (1.20 vs. 1.46 g/L; p<0.001). Across all patients, chemerin positively correlated with BMI, age at diagnosis, c3, c4, CRP, platelet count, and leukocyte count. Hemoglobin and hematocrit were higher in overweight/obese patients, whereas neutrophil ratio was lower and lymphocyte ratio slightly higher. Statin therapy was also more frequent in the overweight/obese group (p=0.04). In this group, BMI and platelet count independently predicted chemerin levels, while platelet count predicted chemerin in normal-weight patients. Conclusion: Despite its positive correlation with BMI, chemerin levels were not significantly higher in overweight/obese patients, suggesting relatively lower levels. This may partly explain their more favorable immunological profile. Increased statin use may also contribute through anti-inflammatory effects.

Indexed as

ChemokinesHydroxymethylglutaryl-CoA Reductase InhibitorsIntercellular Signaling Peptides and ProteinsObesitySjogren's SyndromeAgedBiomarkersBody Mass IndexCross-Sectional StudiesFemaleHumansLipoproteins, LDLMaleMiddle AgedObesity ParadoxPlatelet CountBiomarkersChemokinesHydroxymethylglutaryl-CoA Reductase InhibitorsIntercellular Signaling Peptides and ProteinsLipoproteins, LDLoxidized low density lipoproteinRARRES2 protein, humanadipokinechemerinobesityoxLDLSjögren’s diseasestatin

Identifiers

PMID42835207
PMCPMC13635372

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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.