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<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/"><rdf:Description rdf:about="https://dirros.openscience.si/IzpisGradiva.php?id=28504"><dc:title>IL-6 as an integrative biomarker of residual inflammation and visceral adiposity in psoriasis</dc:title><dc:creator>Merzel Šabović,	Eva Klara	(Avtor)
	</dc:creator><dc:creator>Kraner Šumenjak,	Tadeja	(Avtor)
	</dc:creator><dc:creator>Janić,	Miodrag	(Avtor)
	</dc:creator><dc:subject>interleukin-6</dc:subject><dc:subject>psoriasis</dc:subject><dc:subject>visceral adiposity index</dc:subject><dc:subject>systemic inflammation</dc:subject><dc:subject>obesity</dc:subject><dc:description>Introduction: Psoriatic patients are frequently exposed to residual inflammation and visceral obesity, two factors that synergistically increase cardiometabolic risk. Methods: We evaluated IL-6 as a potential integrative biomarker linking these pathways in a cross-sectional study including 80 patients with well-controlled skin disease and 20 matched healthy controls. Serum IL-6 was measured by ELISA, and visceral adiposity estimated using the Visceral Adiposity Index (VAI). Results: Psoriatic patients displayed significantly higher IL-6 than controls (38.1 pg/mL [35.5–41.3] vs. 21.4 pg/mL [19.5–33.4]; p&lt;0.001). A distinct VAI threshold of 1.3 was identified, above which IL-6 levels rose steeply until VAI 2.2 and then plateaued. Patients with VAI ≥1.3 had markedly higher IL-6 and pro-inflammatory cytokines than those below this cutoff. Random forest regression confirmed IFN-γ, IL-1β, IL-12p70, and IL-17 as dominant predictors of IL-6, while HbA1c, FIB-4, and treatment contributed minimally. Discussion: These findings suggest that IL-6 elevation in psoriasis primarily reflects cytokine-driven residual inflammation, with non-linear amplification once visceral adiposity exceeds a critical threshold. The threshold-dependent IL-6 dynamic highlights a clinically meaningful inflection point, integrating residual inflammation and visceral fat dysfunction, and may guide early cardiometabolic risk stratification and intervention. Prospective validation is warranted.</dc:description><dc:date>2025</dc:date><dc:date>2026-03-23 11:00:09</dc:date><dc:type>Neznano</dc:type><dc:identifier>28504</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
