Centre for Endemic Disease Control, Chinese Centre for Disease Control and Prevention, Harbin Medical University, Harbin City, 150081, Heilongjiang Province, People's Republic of China.
National Health Commission and Education Bureau of Heilongjiang Province, Key Laboratory of Etiology and Epidemiology, Harbin Medical University, Harbin, China.
Eur J Nutr. 2022 Oct;61(7):3571-3583. doi: 10.1007/s00394-022-02907-x. Epub 2022 May 27.
Autoimmune thyroiditis (AIT) is one of the most common autoimmune endocrine diseases. The currently recognized causes are genetic susceptibility, environmental factors and immune disorders. It is important to clarify the pathogenesis for the prevention, diagnosis, treatment of AIT and scientific iodine supplementation. This study analyzed the DNA methylation levels of PRKAA2, ITGA6, PRL and THEM4 genes related to PI3K-AKT signaling pathway, compared the DNA methylation levels between cases and controls from different water iodine levels in Shandong Province of China, and evaluated the contribution of PI3K-AKT signaling pathway-related genes in AIT.
A total of 176 adult AIT patients were included from three different water iodine areas, and 176 healthy controls were included according to gender, age and BMI. According to the results of the Illumina Methylation 850 K BeadChip in our previous research, the significant methylation differences of genes on the PI3K-AKT signaling pathway related to AIT were determined. The MethylTarget™ assay was used to detect the methylation levels of the target genes, and real-time PCR experiments were used to verify the mRNA expression levels.
Compared with the control group, PRKAA2_3 and 15 CpG sites were hyper-methylated. ITGA6 gene and 2 CpG sites were hypo-methylated in AIT cases. The mRNA expression of ITGA6 gene was negatively correlated with the DNA methylation levels of ITGA6 gene and 2 CpG sites. Compared with cases and controls in areas with different water iodine levels, methylation differences were mainly in PRKAA2 and ITGA6 genes. The methylation levels of PRKAA2_1 and PRKAA2_3 were positively correlated with age. The methylation levels of PRL and THEM4 genes were negatively correlated with age. The methylation level of PRKAA2_3 was positively correlated with FT.
In summary, we identified aberrant DNA methylation levels of PRKAA2 and ITGA6 genes related to PI3K-AKT signaling pathway in the blood of AIT patients. Both iodine supplementation after long-term iodine deficiency and iodine excess can affect the DNA methylation levels of PRKAA2 and ITGA6 genes, and the former affects more obviously. In ITGA6 gene, this aberrant epigenetic modification is associated with the increased mRNA expression.
自身免疫性甲状腺炎(AIT)是最常见的自身免疫性内分泌疾病之一。目前公认的病因有遗传易感性、环境因素和免疫紊乱。阐明 AIT 的发病机制对于预防、诊断、AIT 的治疗和科学补碘具有重要意义。本研究分析了与 PI3K-AKT 信号通路相关的 PRKAA2、ITGA6、PRL 和 THEM4 基因的 DNA 甲基化水平,比较了来自中国山东省不同水碘水平的病例和对照之间的 DNA 甲基化水平,并评估了 PI3K-AKT 信号通路相关基因在 AIT 中的作用。
本研究共纳入了来自三个不同水碘地区的 176 例成人 AIT 患者,根据性别、年龄和 BMI 纳入了 176 例健康对照。根据我们之前研究中 Illumina Methylation 850K BeadChip 的结果,确定了与 AIT 相关的 PI3K-AKT 信号通路相关基因的显著甲基化差异。使用 MethylTarget™ assay 检测靶基因的甲基化水平,并通过实时 PCR 实验验证 mRNA 表达水平。
与对照组相比,PRKAA2_3 和 15 个 CpG 位点呈高甲基化。AIT 病例中 ITGA6 基因和 2 个 CpG 位点呈低甲基化。ITGA6 基因的 mRNA 表达与 ITGA6 基因和 2 个 CpG 位点的 DNA 甲基化水平呈负相关。与不同水碘地区的病例和对照相比,甲基化差异主要发生在 PRKAA2 和 ITGA6 基因中。PRKAA2_1 和 PRKAA2_3 的甲基化水平与年龄呈正相关。PRL 和 THEM4 基因的甲基化水平与年龄呈负相关。PRKAA2_3 的甲基化水平与 FT 呈正相关。
综上所述,我们在 AIT 患者的血液中发现了与 PI3K-AKT 信号通路相关的 PRKAA2 和 ITGA6 基因的异常 DNA 甲基化水平。长期碘缺乏和碘过量后补充碘均可影响 PRKAA2 和 ITGA6 基因的 DNA 甲基化水平,前者影响更为明显。在 ITGA6 基因中,这种异常的表观遗传修饰与 mRNA 表达的增加有关。