Vitamin D receptor gene polymorphisms/haplotypes and serum 25(OH)D3 levels in Hashimoto’s thyroiditis

Salvatore Giovinazzo, Teresa M. Vicchio, Rosaria Certo, Angela Alibrandi, Orazio Palmieri, Alfredo Campennì, Salvatore Cannavò, Francesco Trimarchi, Rosaria Maddalena Ruggeri

Research output: Contribution to journalArticle

16 Citations (Scopus)

Abstract

Vitamin D deficiency and/or reduced function, as per certain polymorphisms of the vitamin D receptor (VDR) gene, have been related to several autoimmune disorders. The present study was aimed to investigate the association of Hashimoto’s thyroiditis with vitamin D status and functional polymorphisms (SNPs) of the VDR gene. In this case–control study, 200 euthyroid subjects were enrolled: 100 newly diagnosed HT patients (87 F, 13 M; mean age ± SD 42 ± 15 year) and 100 healthy individuals, matched for age, sex, BMI, and month of blood sampling. Serum 25(OH)D3 was measured by HPLC. The VDR SNPs BsmI, ApaI, and TaqI, in strong linkage disequilibrium with each other, were detected by restriction fragment length polymorphism-PCR. The prevalence of vitamin D deficiency in HT patients was significantly higher than that in the control group (70 vs 18.2 %; p <0.0001), and median serum 25(OH)D3 level was significantly lower in HT patients than controls (median value: 16.2 vs 37.4 ng/ml; p = 0.026). Moreover, there was a significant inverse correlation between serum 25(OH)D3 and TPOAb concentration (r = −0.669; p = 0.034). Contrarily, the genotype distribution of the studied SNPs was not different in the two groups (BsmI p = 0.783; ApaI p = 0.512; TaqI p = 0.471), as was the allelic frequency [f(B) p = 0.776, f(b) p = 0.887; f(A) p = 0.999, f(a) p = 0.999; f(T) p = 0.617; f(t) p = 0.617]. The present study first investigates newly diagnosed untreated HT and suggests that vitamin D deficiency may contribute to HT development and/or progression, acting as an environmental trigger, while the VDR locus does not appear to be involved in conditioning the genetic susceptibility to the disease, at least in Caucasians.

Original languageEnglish
Pages (from-to)1-8
Number of pages8
JournalEndocrine
DOIs
Publication statusAccepted/In press - Apr 4 2016

Fingerprint

Hashimoto Disease
Calcitriol Receptors
Haplotypes
Vitamin D Deficiency
Serum
Genes
Linkage Disequilibrium
Genetic Predisposition to Disease
Vitamin D
Restriction Fragment Length Polymorphisms
Genotype
High Pressure Liquid Chromatography
Polymerase Chain Reaction
Control Groups

Keywords

  • Autoimmunity
  • Hashimoto’s thyroiditis
  • Single nucleotide polymorphisms
  • Vitamin D
  • Vitamin D receptor gene (VDR)

ASJC Scopus subject areas

  • Endocrinology
  • Endocrinology, Diabetes and Metabolism

Cite this

Giovinazzo, S., Vicchio, T. M., Certo, R., Alibrandi, A., Palmieri, O., Campennì, A., ... Ruggeri, R. M. (Accepted/In press). Vitamin D receptor gene polymorphisms/haplotypes and serum 25(OH)D3 levels in Hashimoto’s thyroiditis. Endocrine, 1-8. https://doi.org/10.1007/s12020-016-0942-5

Vitamin D receptor gene polymorphisms/haplotypes and serum 25(OH)D3 levels in Hashimoto’s thyroiditis. / Giovinazzo, Salvatore; Vicchio, Teresa M.; Certo, Rosaria; Alibrandi, Angela; Palmieri, Orazio; Campennì, Alfredo; Cannavò, Salvatore; Trimarchi, Francesco; Ruggeri, Rosaria Maddalena.

In: Endocrine, 04.04.2016, p. 1-8.

Research output: Contribution to journalArticle

Giovinazzo, S, Vicchio, TM, Certo, R, Alibrandi, A, Palmieri, O, Campennì, A, Cannavò, S, Trimarchi, F & Ruggeri, RM 2016, 'Vitamin D receptor gene polymorphisms/haplotypes and serum 25(OH)D3 levels in Hashimoto’s thyroiditis', Endocrine, pp. 1-8. https://doi.org/10.1007/s12020-016-0942-5
Giovinazzo, Salvatore ; Vicchio, Teresa M. ; Certo, Rosaria ; Alibrandi, Angela ; Palmieri, Orazio ; Campennì, Alfredo ; Cannavò, Salvatore ; Trimarchi, Francesco ; Ruggeri, Rosaria Maddalena. / Vitamin D receptor gene polymorphisms/haplotypes and serum 25(OH)D3 levels in Hashimoto’s thyroiditis. In: Endocrine. 2016 ; pp. 1-8.
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