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The DNAm levels of CREB5 (cg11301281) were associated with clopidogrel resistance
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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9550965/ https://www.ncbi.nlm.nih.gov/pubmed/36087301 http://dx.doi.org/10.1002/jcla.24690 |
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author | Li, Jiyi Yang, Jin Yu, Qinglin Chen, Lian Shi, Xiliang Su, Jia Zhu, Keqi |
author_facet | Li, Jiyi Yang, Jin Yu, Qinglin Chen, Lian Shi, Xiliang Su, Jia Zhu, Keqi |
author_sort | Li, Jiyi |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9550965 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95509652022-10-14 The DNAm levels of CREB5 (cg11301281) were associated with clopidogrel resistance Li, Jiyi Yang, Jin Yu, Qinglin Chen, Lian Shi, Xiliang Su, Jia Zhu, Keqi J Clin Lab Anal Research Articles 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. John Wiley and Sons Inc. 2022-09-10 /pmc/articles/PMC9550965/ /pubmed/36087301 http://dx.doi.org/10.1002/jcla.24690 Text en © 2022 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Li, Jiyi Yang, Jin Yu, Qinglin Chen, Lian Shi, Xiliang Su, Jia Zhu, Keqi The DNAm levels of CREB5 (cg11301281) were associated with clopidogrel resistance |
title | The DNAm levels of CREB5 (cg11301281) were associated with clopidogrel resistance |
title_full | The DNAm levels of CREB5 (cg11301281) were associated with clopidogrel resistance |
title_fullStr | The DNAm levels of CREB5 (cg11301281) were associated with clopidogrel resistance |
title_full_unstemmed | The DNAm levels of CREB5 (cg11301281) were associated with clopidogrel resistance |
title_short | The DNAm levels of CREB5 (cg11301281) were associated with clopidogrel resistance |
title_sort | dnam levels of creb5 (cg11301281) were associated with clopidogrel resistance |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9550965/ https://www.ncbi.nlm.nih.gov/pubmed/36087301 http://dx.doi.org/10.1002/jcla.24690 |
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