Polymorphisms in the GCK gene increase the risk of clopidogrel resistance in stable coronary artery disease (SCAD) patients

Background: Diabetes mellitus is a major factor in clopidogrel resistance (CR), and the glucokinase (GCK) gene plays a pivotal role in glucose homeostasis. This study investigated the contribution of GCK polymorphisms to CR risk. Methods: Two hundred SCAD patients were recruited, and their platelet functions were detected by the Verify-Now P2Y12 assay. The polymorphisms of GCK were tested based on the methods of polymerase chain reaction–restriction fragment length polymorphism (PCR-RFLP). We investigated the associations of GCK polymorphisms and CR. Multivariate logistic regression was performed to analyse the correlations between GCK polymorphisms and clinical values. Results: Our study found that the SNPs rs4607517 and rs6975024 were associated with CR. Additionally, patients with the G allele of rs4607517had a greater CR risk, but the C allele of rs6975024 might be a protective factor. Finally, logistic regression revealed that CC + TC (rs6975024) as well as the values of albumin were correlated with a decreased risk of CR, and higher levels of uric acid (UA) may be positively associated with CR. Conclusion: The GCK gene polymorphisms might increase the CR risk in SCAD patients. Meanwhile, higher albumin levels and lower UA values might decrease the risk.

Авторы
Xu H.1 , Yu Q.2 , Zhou H. 3 , Yang J. 3 , Zheng N. 3 , Su J. 3 , Xu Z.4
Журнал
Издательство
Maney Publishing
Номер выпуска
1
Язык
Английский
Страницы
447-452
Статус
Опубликовано
Том
26
Год
2021
Организации
  • 1 Department of Geratology
  • 2 Department of Traditional Chinese Internal Medicine|Ningbo No. 1 Hospital
  • 3 Department of Cardiology
  • 4 Department of Cardiology|Zhenhai People’s Hospital of Zhejiang Province
Ключевые слова
coronary artery disease; platelet aggregation inhibitors; polymorphisms
Дата создания
16.12.2021
Дата изменения
16.12.2021
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/80389/
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