Vascular endothelial growth factor polymorphisms increase the risk of developing Graves' disease

Graves' disease (GD) is a consequence of genetic and environmental factors. Vascular endothelial growth factor (VEGF) is a strong angiogenic and mitogenic factor, which plays a key role in lymphocyte infiltration, and hypervascularization in the thyroid gland of patients with GD. The aim of thi...

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Veröffentlicht in:International immunopharmacology 2012-10, Vol.14 (2), p.133-137
Hauptverfasser: Vural, Pervin, Baki, Merve, Doğru-Abbasoğlu, Semra, Özderya, Ayşenur, Karadağ, Berrin, Uysal, Müjdat
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Sprache:eng
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Zusammenfassung:Graves' disease (GD) is a consequence of genetic and environmental factors. Vascular endothelial growth factor (VEGF) is a strong angiogenic and mitogenic factor, which plays a key role in lymphocyte infiltration, and hypervascularization in the thyroid gland of patients with GD. The aim of this study is to investigate the relationship between GD and A-2578C, T-460C and G+405C single nucleotide polymorphisms (SNPs) of VEGF gene, as well as to evaluate whether there are any relationships between genotypes and some clinical/laboratory parameters of GD. We analyzed the genotype and allele distributions of the above mentioned SNPs in 167 patients with established GD diagnosis and 203 healthy controls by real-time PCR combined with melting curve analysis using fluorescence-labeled hybridization probes. The distribution of VEGF A-2578C and T-460C genotypes and allele frequencies in control and GD groups were not significantly different. With regard to the +405 polymorphism, the frequency of C allele was 1.8-fold increased in GD patients compared to controls, and the CC genotype was associated with a 4.6-fold increased disease risk. There was no relationship between some clinical/laboratory parameters with G+405C polymorphism. However, in −2578C allele carrying GD patients the anti-thyroid antibody levels were increased according to wild homozygous. Additionally, −2578C and −460T alleles were related with early (at age before 40) disease onset. VEGF +405 polymorphism may be a risk factor for GD, while the −2578 SNP is related with increased autoantibody production. ► We investigated the possible relationship between VEGF polymorphisms and GD. ► VEGF −2578, −460 and +405 polymorphisms were assayed by real-time PCR. ► The +405C allele was nearly two-fold increased in GD according to controls. ► −2578C and −460T alleles were related with early (at age before 40) disease onset. ► −2578C allele was related with increased anti-thyroid antibody levels in GD.
ISSN:1567-5769
1878-1705
DOI:10.1016/j.intimp.2012.06.018