Key result
Elevated TNFSF14 links to increased CIMT and identifies newly diagnosed T2DM with a 0.90 AUC.
Why the study?
Data on the relationship between TNFSF14 and carotid intima-media thickness, particularly in newly diagnosed type 2 diabetes mellitus and across age groups, remain limited.
Is circulating TNFSF14 associated with CIMT in newly diagnosed patients with type 2 diabetes mellitus, independent of age?
Cross-Sectional (n=169)
No
Is circulating TNFSF14 associated with CIMT in newly diagnosed patients with type 2 diabetes mellitus, independent of age?
Circulating TNFSF14 levels are significantly elevated in newly diagnosed T2DM and correlate positively with carotid intima-media thickness, suggesting its potential as a supportive biomarker for T2DM and vascular risk regardless of age.
Answers are grounded in this paper and cite their sources.
Supports TNFSF14 as age-independent biomarker for T2DM vascular risk; hypothesis-generating pending longitudinal validation.
Introduction: Tumor necrosis factor superfamily member 14 (TNFSF14) is an immuno-inflammatory biomarker which might play a role in the pathogenesis of type-2 Diabetes Mellitus (T2DM) and also vascular inflammation. Carotid intima-media thickness (CIMT) is a marker of vascular risk and is a well-established marker of subclinical atherosclerosis; however, data on its relationship with TNFSF14, particularly in newly diagnosed T2DM patients, remain limited. Our aim was to investigate the association between TNFSF14 and CIMT in patients with newly diagnosed T2DM and to evaluate whether these markers could serve as supportive indicators for T2DM, including age-based comparison between adult and older patient groups.Methods: This cross-sectional study was conducted at the Internal Medicine Outpatient Clinics of a tertiary hospital. Newly diagnosed T2DM patients and controls without DM were included in the study. Biochemical parameters, TNFSF14 levels and CIMT were measured. Serum TNFSF14 levels were measured using enzyme-linked immunosorbent assay (ELISA), and CIMT was assessed by B-mode ultrasonography. Statistical analyses were performed to determine correlations between TNFSF14, CIMT, and metabolic parameters, and receiver operating characteristic (ROC) analysis was used to evaluate diagnostic performance. Data were assessed in whole group and according to age groups (≥50<years).Results: 79 patients with T2DM and 90 patients without DM were included in the study. TNFSF14, and CIMT levels were significantly higher in patients with T2DM than control group patients (p<0.001). TNFSF14 was positively correlated with CIMT (p<0.001) and showed strong diagnostic performance with an AUC of 0.90 (95%CI, 0.85-0.95, p<0.001) for presence of T2DM. Optimal cut-off value of TNFSF14 for discriminating T2DM was 57.60, 91% sensitivity, 82% specificity. TNFSF14 also showed strong diagnostic performance in both older and adult patient groups as well. CIMT showed moderate diagnostic value for diabetes overall and in those aged 50+, but with poor specificity.Conclusions: CIMT and especially circulating TNFSF14 with a high sensitivity and specificity might be used as supportive markers for T2DM, regardless of age.
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Çavdar et al. (2026) conducted a cross-sectional in Type 2 Diabetes Mellitus (n=169). TNFSF14 vs. Non-diabetic controls was evaluated on CIMT and TNFSF14 level in relation to presence of T2DM (AUC 0.90, 95% CI 0.85-0.95, p=<0.001). TNFSF14 levels and carotid intima-media thickness were significantly higher in newly diagnosed type 2 diabetes patients compared to non-diabetic controls, with TNFSF14 demonstrating strong diagnostic accuracy for T2DM (AUC 0.90, sensitivity 91%, specificity 82%).
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