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Double-Blind, Placebo-Controlled, Randomized Trial of Selenium in Graves Hyperthyroidism
George J Kahaly1, Michaela Riedl1, Jochem König2
1Department of Medicine I, Johannes Gutenberg University Medical Center, 55101 Mainz, Germany.
The Journal of Clinical Endocrinology and Metabolism
|November 2, 2017
Summary
This study found that supplemental selenium (Se) did not improve treatment response or reduce recurrence rates in patients with Graves disease (GD). Selenium supplementation showed no significant benefit for Graves disease management when added to standard medical treatment.
Area of Science:
- Endocrinology
- Nutritional Science
- Immunology
Background:
- Graves disease (GD) is an autoimmune disorder causing hyperthyroidism.
- The role of supplemental selenium (Se) in modulating the clinical course of GD is under investigation.
Purpose of the Study:
- To evaluate the efficacy of add-on selenium supplementation to standard medical treatment for Graves disease.
- To assess the impact of selenium on response rates, recurrence rates, and safety in GD patients.
Main Methods:
- A double-blind, placebo-controlled, randomized supplementation trial was conducted.
- Seventy untreated hyperthyroid GD patients received methimazole (MMI) plus either sodium selenite (300 µg/d) or placebo for 24 weeks.
- Key outcomes included response rate at week 24, recurrence rate at week 36, and safety assessments.
Main Results:
- No significant difference in response rates was observed between the selenium and placebo groups at week 24 (80% vs. 82%, P=0.904).
- Recurrence rates at week 36 were also similar (48% vs. 44%, P=0.81).
- Serum selenium and selenoprotein P levels did not correlate with response or recurrence, and adverse events were comparable between groups.
Conclusions:
- Supplemental selenium did not demonstrate a significant effect on response or recurrence rates in patients with Graves disease.
- The findings suggest that selenium supplementation is not effective as an add-on therapy for GD management.
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