Kuś Aleksander, Szymański Konrad, Peeters Robin P, Miśkiewicz Piotr, Porcu Eleonora, Pistis Giorgio, Sanna Serena, Naitza Silvia, Płoski Rafał, Medici Marco, Bednarczuk Tomasz
Department of Internal Medicine and Endocrinology, Medical University of Warsaw, Warsaw, Poland.
Department of Medical Genetics, Centre for Biostructure, Medical University of Warsaw, Warsaw, Poland.
Clin Endocrinol (Oxf). 2015 Oct;83(4):556-62. doi: 10.1111/cen.12640. Epub 2014 Dec 22.
Despite great progress, the genetic basis of Graves' disease (GD) remains poorly understood. Recently, a population-based genomewide association study (GWAS) identified five novel loci (ATXN2/SH2B3, MAGI3, BACH2, TPO and KALRN) as significantly associated with the presence of thyroid peroxidase autoantibodies (TPOAbs), whereas several other loci showed suggestive association.
In this study, we investigated 16 single nucleotide polymorphisms (SNPs) associated with TPOAbs for the association with susceptibility to and phenotype of GD in a cohort of 647 patients with GD and 769 controls from a Polish Caucasian population.
SNPs within/near HCP5 (rs3094228, P = 1·6 × 10(-12) , OR = 1·88), MAGI3 (rs1230666, P = 1·9 × 10(-5) , OR = 1·51) and ATXN2/SH2B3 (rs653178, P = 0·0015, OR = 1·28) loci were significantly associated with susceptibility to GD. Allele frequencies differed significantly in subgroups of patients with GD stratified by age of GD onset for HCP5 (P = 0·0014, OR = 1·50) and showed a suggestive difference for MAGI3 (P = 0·0035, OR = 1·50) SNPs. Although rs11675434 located near TPO showed no association with GD susceptibility, it was significantly associated with the presence of clinically evident Graves' ophthalmopathy (GO, P = 5·2 × 10(-5) , OR = 1·64), and this effect was independent from smoking status, age of GD onset and gender.
This is the first study showing an association of the ATXN2/SH2B3 locus with susceptibility to GD. Furthermore, we observed a novel significant association within the HLA region at a SNP located near HCP5 and confirmed the association of the MAGI3 locus with GD susceptibility. HCP5 and MAGI3 SNPs were further correlated with age of GD onset. Finally, we identified TPO as a new susceptibility locus for GO.
尽管取得了巨大进展,但格雷夫斯病(GD)的遗传基础仍知之甚少。最近,一项基于人群的全基因组关联研究(GWAS)确定了五个新的基因座(ATXN2/SH2B3、MAGI3、BACH2、TPO和KALRN)与甲状腺过氧化物酶自身抗体(TPOAbs)的存在显著相关,而其他几个基因座显示出提示性关联。
在本研究中,我们在一组来自波兰白种人群的647例GD患者和769例对照中,研究了与TPOAbs相关的16个单核苷酸多态性(SNP)与GD易感性和表型的关联。
HCP5内/附近的SNP(rs3094228,P = 1.6×10⁻¹²,OR = 1.88)、MAGI3(rs1230666,P = 1.9×¹⁰⁻⁵,OR = 1.51)和ATXN2/SH2B3(rs653178,P = 0.0015,OR = 1.28)基因座与GD易感性显著相关。对于HCP5,按GD发病年龄分层的GD患者亚组中,等位基因频率有显著差异(P = 0.0.0014,OR = 1.50),而MAGI3 SNP显示出提示性差异(P = 0.0035,OR = 1.50)。尽管位于TPO附近的rs11675434与GD易感性无关,但它与临床明显的格雷夫斯眼病(GO)的存在显著相关(P = 5.2×10⁻⁵,OR = 1.64),且这种效应独立于吸烟状态、GD发病年龄和性别。
这是第一项显示ATXN2/SH2B3基因座与GD易感性相关的研究。此外,我们在HCP5附近的一个SNP处观察到HLA区域内有一个新的显著关联,并证实了MAGI3基因座与GD易感性的关联。HCP5和MAGI3 SNP与GD发病年龄进一步相关。最后,我们确定TPO是GO的一个新的易感基因座。