ArticleFrontiers in endocrinology2025
Adipose tissue IL-23 is associated with fasting blood glucose and HbA1c in overweight/obese individuals.
Article in Frontiers in endocrinology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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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.
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1 citing paper in PubMed.
- Metabolic Complications in Autoimmune and Autoinflammatory Diseases: Pathophysiology, Clinical Implications, and Therapeutic Perspectives.Journal of clinical medicine · 2026Review
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8 authors.
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Abstract
IL-23, a proinflammatory cytokine, plays a role in the development of inflammatory diseases. However, the association between IL-23 expression in adipose tissue (AT) and glycemic changes in obesity remains unclear. This cross-sectional study aimed to examine the relationship of adipose tissue IL-23 (AT-IL-23) expression with other inflammatory mediators within the same compartment and insulin resistance markers fasting blood glucose (FBG) and glycated hemoglobin (HbA1c) in overweight/obese individuals. Fat biopsies were collected from 10 individuals with a body mass index (BMI) < 25kg/m2 and 51 individuals with a BMI > 25kg/m2 and were analyzed for IL-23 and other inflammatory markers using qRT-PCR. Inflammatory markers, including CD16, CD11c, CCR2, CCR5, TNF-α, IL-1β, IL-2, IL-12, CCL8, CCL19, and CXCL9, were positively correlated with IL-23 in the AT-compartment in the obesity context. Notably, AT-IL-23 was correlated positively with FBG, HbA1c, and homeostasis model assessment of insulin resistance (HOMA-IR), while negatively correlating with adiponectin. These findings suggest that AT-IL-23 is associated with metabolic inflammation and insulin resistance in obesity, suggesting it may be of interest for future biomarker studies.
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