Key result
FPG and HbA1c are linked to new DNA methylation CpG sites in adult monozygotic twins.
Why the study?
The study aimed to identify CpG sites associated with fasting plasma glucose and HbA1c to explore the potential DNA methylation mechanisms of blood glucose metabolism.
Observational (n=338)
Yes
p-value: p=<0.001
The study identifies novel DNA methylation sites associated with fasting glucose and HbA1c in monozygotic twins, providing insights into the epigenetic mechanisms of glucose metabolism.
OBJECTIVE: To explore the cytidine-phosphate-guanosine (CPG) sites associated with fas-ting plasma glucose (FPG) and glycated haemoglobin (HbA1c) in twins. METHODS: In the study, 169 pairs of monozygotic twins were recruited in Qingdao, Zhejiang, Jiangsu, Sichuan and Heilongjiang in June to December of 2013 and June 2017 to October 2018. The methylation was detected by Illumina Infinium HumanMethylation450 BeadChip and Illumina Infinium MethylationEPIC BeadChip. According to the Linear Mixed Effect model (LME model), fasting plasma glucose and HbA1c were taken as the main effects, the methylation level (β value) was taken as the dependent variable, continuous variables, such as age, body mass index (BMI), blood pressure, components of blood cells, surrogate variables generated by SVA, and categorical variables, such as gender, smoking and drinking status, hypoglycemic drugs taking, were included in the fixed effect model as covariates, and the identity numbers (ID) of the twins was included in the random effect model. The intercept was set as a random. Regression analysis was carried out to find out the CpG sites related to fasting blood glucose or HbA1c, respectively. CONCLUSION: In this twin study, we found new CpG sites related to fasting blood glucose and HbA1c, and provided some clues that partly revealed the potential mechanism of blood glucose metabolism in terms of DNA methylation, but it needed further verification in external larger samples.
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A 2020 study reported an observational. Fasting plasma glucose and HbA1c was evaluated on CpG sites related to fasting blood glucose or HbA1c (p=<0.001). Fasting plasma glucose and HbA1c levels were significantly associated with new DNA methylation CpG sites in adult monozygotic twins (P<0.001).
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