Selenium supplementation in patients with subclinical hypothyroidism affected by autoimmune thyroiditis: Results of the SETI study

Endocrinol Diabetes Nutr (Engl Ed). 2020 Jan;67(1):28-35. doi: 10.1016/j.endinu.2019.03.018. Epub 2019 Jun 10.
[Article in English, Spanish]

Abstract

Objective: The purpose of this prospective study was to assess the effects of selenium supplementation on TSH and interferon-γ inducible chemokines (CXCL9, CXCL10 and CXCL11) levels in patients with subclinical hypothyroidism due to Hashimoto's thyroiditis.

Patients and methods: Patients with subclinical hypothyroidism due to Hashimoto thyroiditis were prospectively enrolled in the SETI study. They received 83mcg of selenomethionine/day orally in a soft gel capsule for 4 months with water after a meal. No further treatment was given. All patients were measured thyroid hormone, TPOAb, CXCL9, CXCL10, CXCL11, iodine, and selenium levels at baseline and at study end.

Results: 50 patients (43/7 female/male, median age 43.9±11.8 years) were enrolled, of which five withdrew from the study. At the end of the study, euthyroidism was restored in 22/45 (48.9%) participants (responders), while 23 patients remained hypothyroid (non-responders). There were no significant changes in TPOAb, CXCL9, CXCL10, CXCL11, and iodine levels from baseline to the end of the study in both responders and non-responders. TSH levels were re-tested six months after selenomethionine withdrawal: 83.3% of responding patients remained euthyroid, while only 14.2% of non-responders became euthyroid.

Conclusions: The SETI study shows that short-course supplementation with selenomethionine is associated to a normalization of serum TSH levels which is maintained 6 months after selenium withdrawal in 50% of patients with subclinical hypothyroidism due to chronic autoimmune thyroiditis. This TSH-lowering effect of selenium supplementation is unlikely to be related to changes in humoral markers of autoimmunity and/or circulating CXCL9.

Keywords: Hipotiroidismo; Hypothyroidism; Interferon-γ inducible chemokines; Quimiocinas inducibles por interferón γ; Selenium supplementation; Suplementos de selenio.

MeSH terms

  • Administration, Oral
  • Adult
  • Aged
  • Analysis of Variance
  • Antibodies / blood
  • Autoantigens / immunology
  • Chemokine CXCL10 / blood
  • Chemokine CXCL11 / blood
  • Chemokine CXCL2 / blood
  • Female
  • Hashimoto Disease / blood
  • Hashimoto Disease / complications*
  • Humans
  • Hypothyroidism / blood*
  • Hypothyroidism / etiology
  • Hypothyroidism / therapy
  • Interferon-gamma
  • Iodide Peroxidase / immunology
  • Iodine / blood
  • Iron-Binding Proteins / immunology
  • Logistic Models
  • Male
  • Middle Aged
  • Prospective Studies
  • ROC Curve
  • Selenium / blood*
  • Selenomethionine / administration & dosage*
  • Thyrotropin / blood
  • Treatment Outcome
  • Young Adult

Substances

  • Antibodies
  • Autoantigens
  • CXCL10 protein, human
  • CXCL11 protein, human
  • CXCL2 protein, human
  • Chemokine CXCL10
  • Chemokine CXCL11
  • Chemokine CXCL2
  • Iron-Binding Proteins
  • Interferon-gamma
  • Thyrotropin
  • Selenomethionine
  • Iodine
  • TPO protein, human
  • Iodide Peroxidase
  • Selenium