Department of Biomedical Informatics, Division of Health Sciences, Osaka University Graduate School of Medicine, Yamadaoka 1-7, Suita, Osaka 565-0871, Japan.
Department of Biomedical Informatics, Division of Health Sciences, Osaka University Graduate School of Medicine, Yamadaoka 1-7, Suita, Osaka 565-0871, Japan.
Cytokine. 2019 Nov;123:154770. doi: 10.1016/j.cyto.2019.154770. Epub 2019 Jul 3.
The intractability of Graves' disease (GD) and the severity of Hashimoto's disease (HD) vary among patients. Both genetic and environmental factors may be associated with their prognoses. To clarify the role of methylation of the IFNG gene in the pathogenesis and prognosis of (AITDs), we examined interferon gamma (IFNG) methylation levels at various CpG sites and genotyped IFNG +874 A/T and +2109 C/T polymorphisms. We analyzed methylation 59 patients with HD, 57 patients with GD and 26 healthy volunteers by pyrosequencing. We genotyped IFNG gene polymorphisms from 207 patients with GD, 208 patients with HD, and 102 healthy controls. The methylation levels of IFNG -54 CpG were higher in patients with intractable GD than in those with GD in remission, but there was no difference between patients with severe and mild HD. In carriers of IFNG +2109 T (CT + TT) (85.5% in controls), the -54 CpG methylation levels were significantly higher in patients with intractable GD than in those with GD in remission. On the other hand, in carriers of IFNG +2109 CC, the -4293 CpG methylation levels were higher in intractable GD patients. The methylation levels of IFNG -54 CpG and -4293 CpG were negatively correlated with the age in HD, especially severe HD, patients and GD patients, respectively. There was no circadian variation but considerable daily variation in the methylation levels of IFNG -54 CpG. In conclusion, both the methylation levels of CpG sites and the functional polymorphisms in the IFNG gene were associated with the pathogenesis and prognosis of AITD, especially with GD intractability.
格雷夫斯病(GD)的难治性和桥本甲状腺炎(HD)的严重程度在患者之间存在差异。遗传和环境因素都可能与它们的预后有关。为了阐明 IFNG 基因甲基化在自身免疫性甲状腺疾病(AITD)发病机制和预后中的作用,我们检测了干扰素γ(IFNG)在不同 CpG 位点的甲基化水平,并对 IFNG+874A/T 和+2109C/T 多态性进行了基因分型。我们通过焦磷酸测序分析了 59 例 HD 患者、57 例 GD 患者和 26 名健康志愿者的 IFNG 基因甲基化水平。我们从 207 例 GD 患者、208 例 HD 患者和 102 名健康对照中基因分型 IFNG 基因多态性。难治性 GD 患者 IFNG-54 CpG 的甲基化水平高于缓解期 GD 患者,但严重和轻度 HD 患者之间无差异。在 IFNG+2109T(CT+TT)携带者(对照组中为 85.5%)中,难治性 GD 患者 IFNG-54 CpG 的甲基化水平明显高于缓解期 GD 患者。另一方面,在 IFNG+2109CC 携带者中,难治性 GD 患者 IFNG-4293 CpG 的甲基化水平较高。IFNG-54 CpG 和-4293 CpG 的甲基化水平与 HD 患者,特别是严重 HD 患者和 GD 患者的年龄呈负相关。IFNG-54 CpG 的甲基化水平无昼夜变化,但有明显的日间变化。总之,CpG 位点的甲基化水平和 IFNG 基因的功能多态性与 AITD 的发病机制和预后有关,尤其是与 GD 的难治性有关。