دورية أكاديمية

Fas ligand gene polymorphisms are not associated with Hashimoto’s thyroiditis and Graves’ disease

التفاصيل البيبلوغرافية
العنوان: Fas ligand gene polymorphisms are not associated with Hashimoto’s thyroiditis and Graves’ disease
المؤلفون: Stuck, Bettina J.1, Pani, Michael A.1, Besrour, Foued1, Segni, Maria2, Krause, Maren1, Usadel, Klaus-H.1, Badenhoop, Klaus1 badenhoop@em.uni-frankfurt.de
المصدر: Human Immunology. Feb2003, Vol. 64 Issue 2, p285. 5p.
مصطلحات موضوعية: *THYROIDITIS, *AUTOIMMUNITY
مستخلص: Hashimoto’s thyroiditis and Graves’ disease represent the two most common autoimmune thyroid disorders. Whereas in Hashimoto’s thyroiditis FasL expression causes thyrocytes to undergo apoptosis, additional anti-apoptotic molecules appear to protect these cells in Graves’ disease. Mutations of the FasL gene were observed in systemic lupus erythematosus. Given its functional relevance for the pathogenesis of thyroid autoimmunity we wondered whether variants of the FasL gene play a role in Hashimoto’s thyroiditis and Graves’ disease. We genotyped families with at least one offspring affected by Hashimoto’s thyroiditis (n = 86) and Graves’ disease (n = 90) for two FasL gene polymorphisms (C -843 T in the promoter, A IVS2nt-124 G in intron 2). Extended transmission disequilibrium (ETDT) and χ2 testing were performed. Neither polymorphism alone nor the promoter/intron 2 haplotypes (p = 0.91) were associated with Hashimoto’s thyroiditis. No association with Graves’ disease was observed for the promoter polymorphism (p = 0.91) and the intron 2 “A” allele (57.1%; p = 0.36) or the promoter/intron 2 haplotypes (p = 0.31). Moreover, intron 2 genotyping revealed no difference between an additional 251 patients with Graves’ disease and 197 healthy controls (p = 0.37). Italian and German families did not differ for the studied polymorphisms. In conclusion, our data do not suggest common genetic FasL variants to significantly contribute to the pathogenesis of either Hashimoto’s thyroiditis or Graves’ disease. [Copyright &y& Elsevier]
قاعدة البيانات: Academic Search Index
الوصف
تدمد:01988859
DOI:10.1016/S0198-8859(02)00775-9