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Summaryobjective  Vitamin D modulates the immune system by suppressing the proliferation of activated T cells, with its actions being directed through the vitamin D receptor (VDR). A number of single nucleotide polymorphisms (SNPs) have been identified in the VDR gene, of which several have been associated with autoimmune diseases, including type 1 diabetes and Graves’ disease (GD) in Japanese females. The aim of this study was to test for association of polymorphisms of the VDR gene in the genetic susceptibility to GD in UK Caucasians.design  Target DNA for five previously published SNPs, four novel SNPs and one microsatellite marker was amplified by the polymerase chain reaction (PCR). Subsequent genotyping was performed using restriction fragment length polymorphism (RFLP) or microsatellite genotyping analysis, according to the type of VDR polymorphism.patients  We obtained DNA from a case–control dataset consisting of 768 patients with GD and 864 control subjects. All patients and control subjects were Caucasians born in the UK, and all gave informed, written consent.measurements  Frequencies of the alleles and genotypes of the ten VDR gene polymorphisms were compared between patients and control subjects using the χ2 test. Odds ratios were calculated using Woolf's method with Haldane's modification for small numbers and D prime (D′) was calculated to assess the level of linkage disequilibrium (LD) between the ten polymorphisms.results  No differences in allele or genotype frequencies were observed between GD cases and control subjects for any of the nine SNPs studied. The S allele of the PolyA microsatellite marker was slightly more frequent in GD cases when compared with control subjects (χ2= 4·364, P = 0·04). Strongest LD between markers was observed towards the 3′ end of the VDR gene but there was no evidence of association with disease.conclusion  This is the largest and most comprehensive study of the VDR gene in GD to date and these data suggest that these polymorphisms of the VDR gene do not contribute to GD susceptibility in the UK.

Original publication

DOI

10.1111/j.1365-2265.2004.02015.x

Type

Journal article

Journal

Clinical Endocrinology

Publisher

Wiley

Publication Date

05/2004

Volume

60

Pages

618 - 624