Serum selenium levels and subacute thyroiditis: associations with disease course and long-term outcomes in a case-control study
- PMID: 40102831
- PMCID: PMC11916927
- DOI: 10.1186/s12902-025-01903-6
Serum selenium levels and subacute thyroiditis: associations with disease course and long-term outcomes in a case-control study
Abstract
Background: Subacute thyroiditis (SAT) is an inflammatory disease that induces thyrotoxicosis. Selenium is an essential trace element in thyroid physiology, which has anti-inflammatory and antioxidant properties. However, the relationship between serum selenium levels and SAT has not been well studied. The objective of this study was to evaluate serum selenium levels in patients with SAT compared to healthy controls and to investigate potential correlations between selenium status and clinical outcomes, including disease severity, delayed remission, recurrence, and the development of permanent hypothyroidism.
Methods: This case-control study included 59 patients with SAT and 50 healthy control subjects. Serum selenium levels were analysed using inductively coupled plasma mass spectrometry.
Results: The serum selenium levels of patients with SAT were 69.10 (24.60-130.20) µg/L, while those of the control group were 64.20 (39.21-106.80) µg/L (p = 0.121). A negative correlation was detected between serum selenium levels and erythrocyte sedimentation rate, C-reactive protein, neutrophil-to-lymphocyte ratio, free thyroxine, and pain severity. Serum selenium levels did not significantly differ in terms of the response to initial treatment, recurrence, and permanent hypothyroidism.
Conclusion: The study results showed no significant difference in serum selenium levels between patients with SAT and the control group. These results suggest that although lower serum selenium levels may be associated with a more severe and painful SAT course, there is no impact on the long-term prognosis.
Keywords: Granulomatous thyroiditis; Inflammation; Selenium; Thyrotoxicosis; Trace element.
© 2025. The Author(s).
Conflict of interest statement
Declarations. Ethical approval and consent to participate: The study protocol, conducted according to Declaration of Helsinki, was reviewed and approved by the Ethic Commission for Health of University of Health Sciences Diskapi Yildirim Beyazit Training and Research Hospital (Date 19.02.2018 No 46/08). All methods were implemented in compliance with relevant regulations and guidelines. In this study, the purpose and procedures of the study were thoroughly elucidated to all subjects and informed consent was taken prior to participation. Consent for publication: Not applicable. Competing interests: The authors declare no competing interests. Clinical trial number: Not applicable.
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