Key result
Lower CREB5 methylation is linked to clopidogrel resistance in ACS patients with elevated glucose.
Why the study?
Clopidogrel resistance is mostly caused by interindividual variability in platelet inhibition, and the involvement of CREB5 DNA methylation levels in CR among ACS patients treated with clopidogrel was unclear.
Are DNA methylation levels of CREB5 associated with clopidogrel resistance in ACS patients?
Case-Control (n=72)
Are DNA methylation levels of CREB5 associated with clopidogrel resistance in ACS patients?
DNA methylation levels of CREB5 may serve as a biomarker for clopidogrel resistance in ACS patients, particularly those with elevated blood glucose or HbA1c.
May link CREB5 methylation to clopidogrel resistance in ACS; hypothesis-generating and requires validation before any clinical use.
PURPOSE: Clopidogrel resistance (CR) is mostly caused by interindividual variability of the platelet inhibition of clopidogrel, which may induce cardiovascular events. The aim of this research was to evaluate whether DNAm levels of CREB5 (cg01534253) are involved in CR among acute coronary syndrome (ACS) patients treated with clopidogrel. METHODS: 72 patients(36 CR and 36 non-CR) who underwent ACS were included in this study. The VerifyNow P2Y12 assay was selected to evaluate residual platelet reactivity, and bisulfite pyrosequencing methods was used to examine DNA methylation levels on cg01534253. Secondly, CREB5 mRNA expression was analyzed via quantitative real-time PCR. Last, we employed logistic regression to test the interaction between genetic factors of CREB5 methylation and multiple clinical variables in CR patients. RESULTS: Subunit analysis indicated that for patients whose HbA1c levels were ≥6.5% or whose GLU levels were ≥7 mmol/L, lower methylation of cg01534253 indicated a poorer clopidogrel response. In addition, CREB5 mRNA expression was increased in CR patients with GLU levels ≥7 mmol/L. Moreover, regression analysis indicated that the values of albumin and uric acid were correlated with the incidence of CR. CONCLUSIONS: Our findings were likely to provide fresh understanding for the new mechanism of platelet inhibition failure and promote individualized antiplatelet therapy.
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Li et al. (2022) conducted a case-control in Acute coronary syndrome (n=72). DNA methylation levels of CREB5 vs. Higher methylation levels was evaluated on Clopidogrel resistance. Lower DNA methylation of CREB5 was associated with a poorer clopidogrel response in acute coronary syndrome patients with HbA1c ≥6.5% or glucose ≥7 mmol/L.
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