Zaaber Ines, Rancier Marc, Stathopoulou Maria G, Saleh Abdelsalam, Marmouch Héla, Masson Christine, Murray Helena, Kurth Mary Jo, Lamont John, Fitzgerald Peter, Mahjoub Selvia, Said Khaled, Bel Hadj Jrad Tensaout Besma, Mestiri Souhir, Visvikis-Siest Sophie
a UMR INSERM U1122; Interactions Gène-Environnement en Physiopathologie Cardio-Vasculaire (IGE-PCV), Université de Lorraine , Nancy , France .
b Laboratory of Genetics, Biodiversity and Bioresource Valorization , Superior Institute of Biotechnology of Monastir, University of Monastir , Monastir , Tunisia .
Autoimmunity. 2016 Jun;49(4):229-35. doi: 10.3109/08916934.2016.1151005. Epub 2016 Mar 8.
Autoimmune thyroid diseases (AITD), including Graves' disease (GD) and Hashimoto thyroiditis (HT), are complex multifactorial diseases. Vascular endothelial growth factor (VEGF) is implicated in various inflammatory diseases, especially autoimmune diseases. Our aim was to elucidate the relationships between plasma VEGF levels and four genome-wide association study-identified single nucleotide polymorphisms (SNPs) related to VEGF with AITD in Tunisian patients. A total of 364 healthy controls and 389 patients with AITD were genotyped for the SNPs rs6921438, rs4416670, rs6993770 and rs10738760. Levels of thyroid hormones and antibodies were quantified simultaneously with plasma VEGF after a period of six months of treatment. We found that the minor alleles of rs10738760 and rs6921438 are associated with the presence of GD. A allele of rs10738760 polymorphism is associated with increased plasma levels of free tri-iodothyronin (FT3) while no relationship was found with circulating VEGF plasma levels after six months of treatment. We also showed that the T allele of rs4416670 polymorphism was associated with increased risk of hyperthyroidism in patients treated for six months, independently of their initial diagnosis. There was no significant association between the SNPs and the risk for HT compared with controls. This study shows that AITD are influenced by 3 SNPs linked to VEGF circulating levels. Whereas rs10738760 appeared specific to GD and FT3 production after six months of treatment, rs6921438 and rs4416670 were implicated in the risk for GD. This study opens new ways to test pharmacogenomics concepts in the future especially in GD in which recurrence prognosis is still challenging.
自身免疫性甲状腺疾病(AITD),包括格雷夫斯病(GD)和桥本甲状腺炎(HT),是复杂的多因素疾病。血管内皮生长因子(VEGF)与多种炎症性疾病有关,尤其是自身免疫性疾病。我们的目的是阐明突尼斯患者血浆VEGF水平与全基因组关联研究确定的与VEGF相关的四个单核苷酸多态性(SNP)与AITD之间的关系。对364名健康对照者和389名AITD患者进行了rs6921438、rs4416670、rs6993770和rs10738760这几个SNP的基因分型。经过六个月的治疗后,同时对甲状腺激素和抗体水平以及血浆VEGF进行了定量分析。我们发现rs10738760和rs6921438的次要等位基因与GD的存在有关。rs10738760多态性的A等位基因与游离三碘甲状腺原氨酸(FT3)血浆水平升高有关,而在治疗六个月后未发现与循环VEGF血浆水平存在关联。我们还表明,rs4416670多态性的T等位基因与治疗六个月的患者甲状腺功能亢进风险增加有关,与他们的初始诊断无关。与对照组相比,这些SNP与HT风险之间没有显著关联。这项研究表明,AITD受与VEGF循环水平相关的3个SNP影响。虽然rs10738760在治疗六个月后似乎对GD和FT3产生具有特异性,但rs6921438和rs4416670与GD风险有关。这项研究为未来测试药物基因组学概念开辟了新途径,尤其是在复发预后仍具有挑战性的GD中。