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Chinese Journal of Clinical Pharmacology and Therapeutics ›› 2018, Vol. 23 ›› Issue (4): 477-480.doi: 10.12092/j.issn.1009-2501.2018.04.019

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Advances in the relationship between cytochrome P450 SNP and susceptibility to coronary heart disease

PENG Qiuju 1,2, YAN Huacheng 1, SHI Lei 1   

  1. 1 Department of Pharmacy, Guangzhou General Hospital of Guangzhou Military Command, Guangzhou 510010, Guangdong,China; 2 College of Pharmacy, Guangdong Pharmaceutical University, Guangzhou 510006, Guangdong, China
  • Received:2017-08-30 Revised:2017-09-27 Online:2018-04-26 Published:2018-04-13

Abstract:

Coronary heart disease (CHD) is caused by genetic environmental interaction. Studies have shown that cytochrome P450 (CYP) metabolites such as epoxyeicosatrienoic acids (EETs), 20-hydroxy-eicosatetraenoic acid (20-HETE) and sex hormones play important roles in maintaining cardiovascular homeostasis. In vivo, CYP2C19 and CYP2J2 catalyze the metabolism of arachidonic acid (AA) to EETs; CYP4F2 and CYP1A1 are the main synthetases of 20-HETE; CYP17A1 and CYP19 are important synthetases of sex hormones. Therefore, polymorphism of the above CYP genes is likely to affect the development of CHD by influencing the production of its metabolites. This article reviews the five years' advances in the relationship between cytochrome P450 SNP and susceptibility to coronary heart disease so as to provide referential ideas for the personalized treatment of CHD.

Key words: coronary heart disease, polymorphism, cytochrome P450, susceptibility

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