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Effect of Vitamin D Supplementation on Graves' Disease: The DAGMAR Trial.
Grove-Laugesen, Diana; Ebbehoj, Eva; Watt, Torquil; Riis, Anne Lene; Østergård, Torben; Bruun, Bjarke Johannessen; Juel Christiansen, Jens; Hansen, Klavs Würgler; Rejnmark, Lars.
Afiliación
  • Grove-Laugesen D; Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus N, Denmark.
  • Ebbehoj E; Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus N, Denmark.
  • Watt T; Department of Internal Medicine, Herlev Hospital, Herlev, Hovedstaden, Denmark.
  • Riis AL; Medical Department, Regionshospitalet Horsens, Horsens, Midtjylland, Denmark.
  • Østergård T; Medical Department, Aalborg University Hospital, Aalborg, North Denmark Region, Denmark.
  • Bruun BJ; Department of Internal Medicine, Regional Hospital Randers, Randers, Denmark.
  • Juel Christiansen J; Medical Department, Gødstrup Regional Hospital, Herning, Denmark.
  • Hansen KW; Medical Department, Regional Hospital Silkeborg, Silkeborg, Denmark.
  • Rejnmark L; Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus N, Denmark.
Thyroid ; 33(9): 1110-1118, 2023 09.
Article en En | MEDLINE | ID: mdl-37218433
Objective: Treatment options in Graves' disease (GD) are limited and do not target the underlying autoimmunity, and relapse rates following a course of antithyroid drug (ATD) reach 50%. Previous research has shown promising results for a role of vitamin D in GD. We aimed to investigate whether vitamin D reduces failure to enter and sustain remission in patients with GD treated with ATD. Design: A multicenter, double-blinded, randomized placebo-controlled trial comparing vitamin D 70 mcg once daily (2800 IU) or placebo. The intervention was given first as add-on to ATD treatment, maximally 24 months, and then for 12 months after ATD cessation. Inclusion period was from 2015 to 2017 and study completion by December 2020. Patients included were adults with a first-time diagnosis of GD treated with ATD. Exclusion criteria included pregnancy and glucocorticoid treatment. The primary endpoint was failure to enter and sustain remission defined as relapse of hyperthyroidism within 12 months after ATD cessation, inability to stop ATD within 24 months, or radioiodine treatment or thyroidectomy. Two hundred seventy-eight patients were included in the study, and 4 patients withdrew consent. No adverse effects were found. Results: Participants were aged 44 ± 14 years at enrollment and 79% were female. The risk of failure to enter and sustain remission was 42% [95% confidence interval (CI) 33-50%] in the vitamin D group and 32% [CI 24-40%] in the placebo group corresponding to a relative risk of 1.30 [CI 0.95-1.78]. Conclusions: Vitamin D supplementation did not improve the treatment of GD in patients with normal or insufficient vitamin D status. Thus, supplementation with high-dose vitamin D cannot be recommended for GD. Study registration: ClinicalTrials.gov NCT02384668.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedad de Graves / Radioisótopos de Yodo Tipo de estudio: Clinical_trials / Diagnostic_studies / Etiology_studies Idioma: En Revista: Thyroid Año: 2023 Tipo del documento: Article País de afiliación: Dinamarca

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedad de Graves / Radioisótopos de Yodo Tipo de estudio: Clinical_trials / Diagnostic_studies / Etiology_studies Idioma: En Revista: Thyroid Año: 2023 Tipo del documento: Article País de afiliación: Dinamarca