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Graves' disease (GD) is an autoimmune thyroid disease of unknown etiology, although predisposition to the development of this disease is thought to be caused by both genetic and environmental factors. Recently, an association between a promoter polymorphism of the interleukin 4 gene and GD has been reported. A C-T base change at position -590 showed modest protection against the development of GD in a United Kingdom data set of 135 patients with GD and 101 controls. This polymorphism was, therefore, investigated in a much larger case-control cohort of 384 patients with GD and 288 control subjects using PCR, followed by restriction fragment length polymorphism analysis. No protective effect of the T allele of this polymorphism was observed in our data set, and indeed no significant difference in either allelic or genotypic distribution was seen between the patient and control groups. Moreover, calculation of probabilities indicate that the original study lacked sufficient power to support the conclusions drawn. Our data support the hypothesis that the C-T promoter polymorphism of the interleukin 4 gene does not confer protection against the development of GD in Caucasians in the United Kingdom.

Original publication

DOI

10.1210/jcem.86.8.7744

Type

Journal article

Journal

J Clin Endocrinol Metab

Publication Date

08/2001

Volume

86

Pages

3861 - 3863

Keywords

Alleles, Case-Control Studies, Chromosome Mapping, Chromosomes, Human, Pair 18, Cohort Studies, DNA, European Continental Ancestry Group, Gene Frequency, Genotype, Graves Disease, Humans, Interleukin-4, Point Mutation, Polymerase Chain Reaction, Polymorphism, Genetic, Polymorphism, Restriction Fragment Length, Promoter Regions, Genetic, Reference Values, United Kingdom