Department of Endocrinology, Genetics and Metabolism, Children's Hospital of Soochow University, Suzhou, China.
Department of Biochemistry and Molecular Biology, School of Medical and Biological Sciences, Soochow University, Suzhou, China.
Front Endocrinol (Lausanne). 2021 Jun 23;12:691326. doi: 10.3389/fendo.2021.691326. eCollection 2021.
Graves' disease (GD) is the most common cause of hyperthyroidism, yet a relatively rare disease in the pediatric population. GD is a complex disorder influenced by both genetic and environmental factors. In this study, we aimed to find new environmental factors influencing the pathogenesis of GD. We investigated serum substances in 30 newly diagnosed GD children and 30 age- and gender-matched healthy controls. We measured total iodine by inductively coupled plasma-mass spectrometry (ICP-MS), analyzed perfluorinated compounds ultra-high-performance liquid chromatography coupled with multiple reaction monitoring mass spectrometry (UHPLC-MRM-MS), and explored other environmental substances using ultra-high-performance liquid chromatography-quadrupole time-of-flight mass spectrometry (UHPLC-QTOF/MS) analysis. Twenty-nine single-nucleotide polymorphisms (SNPs) in eight genes related to GD were analyzed by SNaPshot. The serum total iodine was significantly higher in GD group, but its association with GD onset was weak, only with Exp(B) value near 1. The perfluorinated compound levels were not different between the two groups. More importantly, we found 16 environmental substances significantly different between GD and control groups, among which ponasterone A is a risk factor ( = 0.007 and Exp(B) = 14.14), while confertifoline is a protective factor against GD onset ( = 0.002 and Exp(B) = 0.001). We also identified 10 substances correlated significantly with thyroid indices in GD patients, among which seven associated with levels of the thyroid autoantibody TPOAb. No known SNPs were found predisposing GD. In this study, we explored a broad variety of environmental substances and identified novel factors that are potentially involved in the pediatric GD pathogenesis.
格雷夫斯病(GD)是最常见的甲状腺功能亢进症的病因,但在儿科人群中相对少见。GD 是一种受遗传和环境因素共同影响的复杂疾病。在这项研究中,我们旨在寻找影响 GD 发病机制的新环境因素。我们检测了 30 名新诊断的 GD 儿童和 30 名年龄和性别匹配的健康对照者的血清物质。我们通过电感耦合等离子体质谱法(ICP-MS)测量总碘,通过超高效液相色谱-串联质谱法(UHPLC-MRM-MS)分析全氟化合物,并用超高效液相色谱-四极杆飞行时间质谱法(UHPLC-QTOF/MS)分析其他环境物质。分析了与 GD 相关的八个基因中的 29 个单核苷酸多态性(SNP)。GD 组的血清总碘明显升高,但与 GD 发病的相关性较弱,仅接近 1 的 Exp(B)值。两组间的全氟化合物水平无差异。更重要的是,我们发现 GD 组和对照组之间有 16 种环境物质存在显著差异,其中波纳酮 A 是一个危险因素( = 0.007 和 Exp(B)= 14.14),而考非停是 GD 发病的保护因素( = 0.002 和 Exp(B)= 0.001)。我们还发现 10 种物质与 GD 患者的甲状腺指数显著相关,其中 7 种与甲状腺自身抗体 TPOAb 的水平相关。未发现已知的 SNP 与 GD 易感性相关。在这项研究中,我们探索了广泛的环境物质,并确定了可能参与儿科 GD 发病机制的新因素。