Abstract
Adhesion molecules are involved in cell invasion in autoimmune thyroid disease. It was also reported that patients with untreated Graves’ disease (GD) had high serum level of soluble form of E-selectin (sE-selectin), the concentration of which correlated with the activity of the disease. The aim of the present study was to elucidate whether the common variants in E-selectin gene (SELE) were associated with the development of GD. Six tagSNPs within SELE were studied in 297 patients with GD and 208 healthy subjects in Chinese population. Our data showed that common SELE variants were associated with GD (P=0.012–0.036). Haplotype analysis of the single nucleotide polymorphisms revealed an association of a haplotype ATAACC with GD (P=0.005). Furthermore, quantitative trait analysis showed a significant association of SELE haplotype with sE-selectin levels (P=0.0438). This study therefore could provide us to a certain degree the insight that common SELE variants may be associated with susceptibility to GD in Chinese population, though the limitation of sample size and multiple test problems exists.
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Acknowledgements
The present study would not have been possible without the participation of the patients and healthy volunteers. The study is supported by the grants from the E-Institute of Shanghai Universities (no. E03007) and Shanghai Leading Academic Discipline Project (Project no. Y0204).
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Chen, H., Cui, B., Wang, S. et al. The common variants of E-selectin gene in Graves’ disease. Genes Immun 9, 182–186 (2008). https://doi.org/10.1038/sj.gene.6364452
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DOI: https://doi.org/10.1038/sj.gene.6364452
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