Abstract

Aim. This study aimed to compare thyroid functions, thyroid autoantibodies, and the existence of nonthyroidal illness syndrome (NTIS) according to vitamin D level. Materials and Methods. The study included age- and BMI-matched healthy volunteers with and without vitamin D deficiency. In addition, the nonthyroidal illness syndrome status was evaluated. Results. Anti-TPO positivity was significantly more common in those with severe and moderate vitamin D deficiency, as compared to those with a normal 25(OH)D level. Furthermore, TSH levels were significantly lower in those with severe and moderate vitamin D deficiency than in those with a normal 25(OH)D level. In addition, there was a significant weak inverse correlation between anti-TPO positivity and the 25(OH)D level and a positive correlation between the TSH level and 25(OH)D level. Only 1 thyroid function test result was compatible with NTIS among the participants with moderate vitamin D deficiency; therefore the difference was not significant. Conclusions. The prevalence of thyroid autoantibody positivity was higher in those with severe and moderate vitamin D deficiency than in those with a normal 25(OH)D level. Additional large-scale studies must be conducted to determine if vitamin D deficiency plays a causal role in the pathogenesis of Hashimoto's thyroiditis and NTIS.

Highlights

  • The best-known roles of vitamin D are in calcium metabolism and bone health; accumulating evidence shows that vitamin D has a variety of pro- and anti-inflammatory effects on the development of cancers, autoimmune diseases, and cardiovascular disorders

  • A study on the effect of vitamin D on monocyte expression of tumor necrosis factor-α (TNF-α) showed that 1,25(OH)2D3 could significantly suppress TNF-α, which plays an important role in the pathogenesis of autoimmune

  • The most important finding of the present study is that the prevalence of thyroid autoantibody positivity in healthy volunteers increased as the 25(OH)D level decreased

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Summary

Introduction

The best-known roles of vitamin D are in calcium metabolism and bone health; accumulating evidence shows that vitamin D has a variety of pro- and anti-inflammatory effects on the development of cancers, autoimmune diseases, and cardiovascular disorders. In T helper 2 cells vitamin D increases both the proliferation of interleukin-4 and transforming growth factor that suppresses inflammatory T-cell activation [1, 2, 4]. These interactions are important in the pathogenesis of Hashimoto’s disease. Such proinflammatory cytokines as interleukin-6, TNF-α, and interleukin-1 have been suggested to be mediators in the pathogenesis of nonthyroidal illness syndrome (NTIS) [5]. A study on the effect of vitamin D on monocyte expression of TNF-α showed that 1,25(OH)2D3 could significantly suppress TNF-α, which plays an important role in the pathogenesis of autoimmune

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