Evidence map›Paper›PMID 41857303›Full record

ArticleScientific reports2026

Sex-biased plasma inflammatory protein profile in obesity.

Hilde Halland, Rui Vitorino, Eva Gerdts, Helga Midtbø, Klaus Meyer, Georgios Kararigas

Abstract read
In one paragraph

Article in Scientific reports, 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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1 · What the graph read from it

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2 · The registry

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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

6 authors.

Hilde HallandCenter for Research on Cardiac Disease in Women, Department of Clinical Science, Bergen, Norway. hilde.halland@uib.no.
Rui VitorinoDepartment of Medical Sciences, University of Aveiro, Aveiro, Portugal.
Eva GerdtsCenter for Research on Cardiac Disease in Women, Department of Clinical Science, Bergen, Norway.
Helga MidtbøCenter for Research on Cardiac Disease in Women, Department of Clinical Science, Bergen, Norway.
Klaus MeyerBevital, Bergen, Norway.
Georgios KararigasDepartment of Basic and Clinical Sciences, Medical School, University of Nicosia, UNIC Athens, Athens, Greece.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Obesity-associated inflammation predisposes to cardiovascular disease (CVD). We investigated the association of biological sex with the plasma inflammatory protein profile in individuals with obesity. Clinical and proteomic data from 450 women and men with a body mass index (BMI) > 27 kg/m² without known CVD participating in the FAT associated CardiOvasculaR dysfunction study were analysed. The Olink Target 96 inflammation panel was employed in biobank samples. Hypertension was more prevalent among men, while age, BMI, and prevalences of obesity, diabetes and smoking did not differ between the sexes (all p > 0.05). In multivariable analyses, obesity was associated with downregulation of interleukin (IL) 7, IL 12 subunit beta, IL 6, and C-X-C motif chemokine 11, and upregulation of sulfotransferase 1A1 and SIR2-like protein 2 in women (all p < 0.05). In men, obesity was associated with downregulation of monocyte chemotactic protein 3, tumour necrosis factor superfamily member 12, IL 10 and protein S100-A12, and upregulation of neurotrophin-3 (all p < 0.05). In sum, the targeted protein profile in obesity differed by biological sex and there was no overlap in the differentially regulated proteins between women and men with obesity. The results suggest that pathophysiological mechanisms in obesity-associated inflammation and immune dysregulation may be sex-biased.

Indexed as

Blood ProteinsInflammationObesityAdultAgedBody Mass IndexFemaleHumansMaleMiddle AgedProteomicsSex FactorsBlood ProteinsBiological sexInflammationObesity.Proteomics

Identifiers

PMID41857303
PMCPMC13139431

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