Epigenetic link between Agent Orange exposure and type 2 diabetes in Korean veterans

被引:0
|
作者
Seo, Sujin [1 ]
Kim, Ye An [2 ]
Lee, Young [3 ]
Kim, Young Jin [4 ]
Kim, Bong-Jo [4 ]
An, Jae Hoon [5 ]
Jin, Heejin [5 ]
Do, Ah Ra [6 ]
Park, Kyungtaek [5 ]
Won, Sungho [1 ,5 ,6 ]
Seo, Je Hyun [3 ]
机构
[1] Seoul Natl Univ, Grad Sch Publ Hlth, Dept Publ Hlth Sci, Seoul, South Korea
[2] Vet Hlth Serv Med Ctr, Dept Internal Med, Div Endocrinol, Seoul, South Korea
[3] Vet Hlth Serv Med Ctr, Vet Med Res Inst, Seoul, South Korea
[4] Natl Inst Hlth, Dept Precis Med, Div Genome Sci, Cheongju, South Korea
[5] Seoul Natl Univ, Inst Hlth & Environm, Seoul, South Korea
[6] Seoul Natl Univ, Coll Nat Sci, Interdisciplinary Program Bioinformat, Seoul, South Korea
来源
FRONTIERS IN ENDOCRINOLOGY | 2024年 / 15卷
基金
新加坡国家研究基金会;
关键词
Agent Orange; ageing; epigenome-wide association study; microvascular complications; Mendelian randomization; type; 2; diabetes; EPIGENOME-WIDE ASSOCIATION; OPERATION RANCH HAND; METHYLATION MICROARRAY DATA; ARYL-HYDROCARBON RECEPTOR; B-INDUCING KINASE; BETA-CELL FAILURE; NF-KAPPA-B; DNA METHYLATION; INSULIN-SECRETION; VIETNAM VETERANS;
D O I
10.3389/fendo.2024.1375459
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Conflicting findings have been reported regarding the association between Agent Orange (AO) exposure and type 2 diabetes. This study aimed to examine whether AO exposure is associated with the development of type 2 diabetes and to verify the causal relationship between AO exposure and type 2 diabetes by combining DNA methylation with DNA genotype analyses. An epigenome-wide association study and DNA genotype analyses of the blood of AO-exposed and AO-unexposed individuals with type 2 diabetes and that of healthy controls were performed. Methylation quantitative trait locus and Mendelian randomisation analyses were performed to evaluate the causal effect of AO-exposure-identified CpGs on type 2 diabetes. AO-exposed individuals with type 2 diabetes were associated with six hypermethylated CpG sites (cg20075319, cg21757266, cg05203217, cg20102280, cg26081717, and cg21878650) and one hypo-methylated CpG site (cg07553761). Methylation quantitative trait locus analysis showed the methylation levels of some CpG sites (cg20075319, cg20102280, and cg26081717) to be significantly different. Mendelian randomisation analysis showed that CpG sites that were differentially methylated in AO-exposed individuals were causally associated with type 2 diabetes; the reverse causal effect was not significant. These findings reflect the need for further epigenetic studies on the causal relationship between AO exposure and type 2 diabetes.
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页数:13
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