Methylation levels of the IL10 gene in peripheral blood are related to the intractability of Graves ' disease

被引:0
|
作者
Kinoshita, Riku [1 ]
Inoue, Naoya [1 ,2 ]
Iwatani, Yoshinori [1 ]
Noguchi, Yusuke [1 ]
Hidaka, Yoh [2 ]
Watanabe, Mikio [1 ]
机构
[1] Osaka Univ, Grad Sch Med, Dept Clin Lab & Biomed Sci, Div Hlth Sci, Yamadaoka 1-7, Suita, Osaka 5650871, Japan
[2] Osaka Univ Hosp, Lab Clin Invest, Yamadaoka 2-15, Suita, Osaka 5650871, Japan
关键词
IL-10; Polymorphism; Methylation; Pyrosequencing; Severity; Intractability; Autoimmune thyroid disease; DNA METHYLATION; INTERLEUKIN-10; GENE; POLYMORPHISM; ASSOCIATION; HYPOMETHYLATION; PROPORTION; EXPRESSION; PROGNOSIS; IL-10;
D O I
10.1016/j.clim.2024.110196
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The prognosis of autoimmune thyroid diseases (AITDs), including Hashimoto's disease (HD) and Graves' disease (GD), is difficult to predict. DNA methylation regulates gene expression of immune mediating factors. Interleukin (IL) -10 is a Th2 cytokine that downregulates inflammatory cytokines produced by Th1 cells. To clarify the role of methylation of the IL10 gene in the prognosis of AITD, we evaluated the methylation levels of two CpG sites in the IL10 promoter using pyrosequencing. The methylation levels of the -185 CpG site of the IL10 gene were related to age and GD intractability in GD patients. Furthermore, the C carrier of the IL10 -592 A/C polymorphism was related to low methylation levels of the -185 CpG site. The methylation levels of the IL10 -185 CpG site of the IL10 gene were related to the intractability of GD and were lower in individuals with the C allele of the IL10 -592 A/C polymorphism.
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页数:5
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