Decreased Alu methylation in type 2 diabetes mellitus patients increases HbA1c levels

被引:4
作者
Thongsroy, Jirapan [1 ,2 ,5 ]
Mutirangura, Apiwat [3 ,4 ]
机构
[1] Walailak Univ, Sch Med, Nakhon Si Thammarat, Thailand
[2] Walailak Univ, Res Ctr Trop Pathobiol, Nakhon Si Thammarat, Thailand
[3] Chulalongkorn Univ, Ctr Excellence Mol Genet Canc & Human Dis, Bangkok, Thailand
[4] Chulalongkorn Univ, Fac Med, Dept Anat, Bangkok, Thailand
[5] Walailak Univ, Sch Med, Nakhon Si Thammarat 80160, Thailand
关键词
aging; Alu; DNA methylation; genomic instability; type; 2; DM; INSULIN-RESISTANCE; DNA-DAMAGE; HYPERGLYCEMIA; LINE-1; ASSOCIATION; MECHANISMS; MANAGEMENT; PATTERNS;
D O I
10.1002/jcla.24966
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Introduction Alu hypomethylation is a common epigenetic process that promotes genomic instability with aging phenotypes, which leads to type 2 diabetes mellitus (type 2 DM). Previously, our results showed significantly decreased Alu methylation levels in type 2 DM patients. In this study, we aimed to investigate the longitudinal changes in Alu methylation levels in these patients.Results We observed significantly decreased Alu methylation levels in type 2 DM patients compared with normal (p = 0.0462). Moreover, our findings demonstrated changes in Alu hypomethylation over a follow-up period within the same individuals (p < 0.0001). A reduction in Alu methylation was found in patients with increasing HbA1c levels (p = 0.0013) and directly correlated with increased HbA1c levels in type 2 DM patients (r = -0.2273, p = 0.0387).Conclusions Alu methylation in type 2 DM patients progressively decreases with increasing HbA1c levels. This observation suggests a potential association between Alu hypomethylation and the underlying molecular mechanisms of elevated blood glucose. Furthermore, monitoring Alu methylation levels may serve as a valuable biomarker for assessing the clinical outcomes of type 2 DM.
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页数:8
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