4.2 Article

Association between the severity of Hashimoto's disease and the functional +874A/T polymorphism in the interferon-γ gene

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ENDOCRINE JOURNAL
卷 53, 期 4, 页码 473-478

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JAPAN ENDOCRINE SOC
DOI: 10.1507/endocrj.K06-015

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IFN-gamma; single nucleotide polymorphism; disease severity; ethnic difference; type 1 helper T cell

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CD8(+)CD25(+)-activated cytotoxic T cells and anti-thyroglobulin antibodies (TgAb) are independently involved in the severity of Hashimoto's disease (HD). Interferon gamma (IFN-gamma) activates cytotoxic T cells. To evaluate the hypothesis that the functional +874A/T polymorphism in the gene encoding IFN-gamma is associated with the severity of HD, we examined the frequencies of this polymorphism in 34 HD patients who developed hypothyroidism (severe HD); 22 untreated, euthyroid HD patients (mild HD); 49 patients With intractable Graves' disease (GD); 16 GD patients in remission; and 57 healthy volunteers. Frequency of the +874T allele, which is associated with high IFN-gamma production, was higher in patients with severe HD than in those with mild HD (odds ratio [OR], 3.5; 95% confidence interval [CI], 1.0-12.4; p = 0.047), but there Was no difference in the frequency between GD patients. The difference in the frequency of +874T was observed in the subset of patients with HD negative for TgAb (OR, 8.4; 95% Cl, 1.2-57.3; p = 0.029) but not in the subset of patients With HD positive for TgAb. Our data indicate that the +874A/T polymorphism in the IFN-gamma gene is associated with severity of HD.

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