Lack of association of VDR gene polymorphisms with thyroid autoimmune disorders: familial and case/control studies

J Clin Immunol. 2008 Jan;28(1):21-5. doi: 10.1007/s10875-007-9124-9. Epub 2007 Oct 18.

Abstract

We study the association between three Vitamin D receptor gene polymorphisms (rs10735810, rs1544410, rs731236) and susceptibility to thyroid autoimmune diseases. Seventy-six affected subjects, belonging to a large family, as well as one hundred unrelated Tunisian patients and one hundred healthy Tunisian controls were genotyped. A family-based association test and a standard chi-square test were used to assess association in family and case-control data, respectively. Our results showed no significant association of the Vitamin D receptor gene polymorphisms with the susceptibility to thyroid autoimmune diseases in the family. Moreover, allele frequencies for the three polymorphisms in the Tunisian population were similar to those reported in the Tunisian control population and none was associated with the disease. These results suggest a lack of association between the Vitamin D receptor gene polymorphisms and susceptibility to thyroid autoimmune diseases in Tunisian population, in agreement with data from the UK, but in conflict with studies from the Far East.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Case-Control Studies
  • Child
  • Female
  • Gene Frequency*
  • Genetic Predisposition to Disease*
  • Genotype
  • Graves Disease / genetics*
  • Haplotypes
  • Humans
  • Male
  • Middle Aged
  • Polymorphism, Genetic*
  • Receptors, Calcitriol / genetics*
  • Thyroiditis, Autoimmune / genetics*
  • Tunisia

Substances

  • Receptors, Calcitriol