Key result
Overt hyperthyroidism is linked to significantly higher fractalkine levels and subclinical atherosclerosis markers.
Why the study?
Fractalkine has been linked to heart failure and atherosclerosis, but its levels and association with cardiovascular risk markers in hyperthyroidism are unclear.
Case-Control (n=82)
Single-blind
No
Absolute Event Rate: 1.77% vs 1.39%
p-value: p=0.010
Serum fractalkine is elevated in treatment-naive hyperthyroidism and correlates with early markers of subclinical atherosclerosis and diastolic dysfunction, highlighting a potential pathway for increased cardiovascular risk in this population.
Fractalkine elevation may signal early cardiovascular risk in hyperthyroidism; leaves open its causal role and utility for risk stratification.
Aims: Hyperthyroidism is a common endocrine disorder with significant cardiovascular (CV) implications.Emerging evidence links fractalkine to both heart failure (HF) and atherosclerosis.We aimed to compare serum fractalkine levels between patients with hyperthyroidism and healthy controls and to investigate its potential association with CV risk markers.Methods: This case-control study included treatment-naive adults with overt hyperthyroidism and age-and sex-matched healthy controls with normal thyroid function tests.Participants with cardiovascular disease or major systemic disorders were excluded.All participants underwent physical examination, hormonal profiling, serum fractalkine measurement, electrocardiography, and echocardiographic assessment using both conventional and tissue Doppler techniques to evaluate left and right ventricular function.Results: The study included 41 treatment-naive patients with overt hyperthyroidism (mean age: 45±12.9years) and 41 age-matched healthy controls (mean age: 45±8.2 years).Patients with hyperthyroidism had significantly higher serum fractalkine levels than healthy controls (p=0.01).Within the hyperthyroid group, fractalkine levels positively correlated with carotid intima-media thickness (CIMT), a marker of subclinical atherosclerosis (r=0.317,p=0.043), and negatively correlated with mitral annular velocity in late diastole (a'), a diastolic parameter indicative of HF with preserved ejection fraction (HFpEF) (r =-0.344, p=0.028).Linear regression analysis identified fractalkine as an independent predictor of increased CIMT and of reduced a'.Conclusions: This study demonstrated that fractalkine levels are elevated in patients with hyperthyroidism and are associated with early markers of CV dysfunction, including subclinical atherosclerosis and HFpEF.
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Atmaca et al. (2026) conducted a case-control in Overt hyperthyroidism (n=82). Overt hyperthyroidism vs. Euthyroid healthy controls was evaluated on Serum log-fractalkine levels (p=0.010). Overt hyperthyroidism was associated with significantly higher serum log-fractalkine levels compared to euthyroid controls (1.77 vs 1.39, p=0.010), and levels correlated with markers of subclinical atherosclerosis.
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