氯吡格雷                        
                
                                
                        
                            CYP2C19型                        
                
                                
                        
                            医学                        
                
                                
                        
                            基因型                        
                
                                
                        
                            内科学                        
                
                                
                        
                            置信区间                        
                
                                
                        
                            优势比                        
                
                                
                        
                            等位基因                        
                
                                
                        
                            胃肠病学                        
                
                                
                        
                            药理学                        
                
                                
                        
                            心肌梗塞                        
                
                                
                        
                            基因                        
                
                                
                        
                            生物                        
                
                                
                        
                            遗传学                        
                
                                
                        
                            细胞色素P450                        
                
                                
                        
                            新陈代谢                        
                
                        
                    
            作者
            
                Yijun Mo,Yao Lu,Fei Guo,Aihua Wu,Yuesong Weng            
         
                    
        
    
            
            标识
            
                                    DOI:10.3389/fcvm.2023.1020593
                                    
                                
                                 
         
        
                
            摘要
            
            Certain genetic and non-genetic factors may cause damaged platelet inhibition by clopidogrel. We aimed to determine the effect of cytochrome P4502C19 (CYP2C19) polymorphism, along with other clinical factors, on the platelet response to clopidogrel in patients with acute ischemic stroke (AIS).A total of 214 patients with AIS receiving clopidogrel at a maintenance dose of 75 mg daily admitted to the Ningbo First Hospital between 1 January 2020, and 31 December 2021, were enrolled. Platelet aggregation analysis was performed to determine clopidogrel resistance. Quantitative real-time polymerase chain reaction (QRT-PCR) was used to determine CYP2C19 genotype. Other laboratory data on complete blood count and biochemical parameters were taken from patient medical files.Among the 214 AIS patients treated with clopidogrel in the Ningbo population, the incidence of clopidogrel resistance was approximately 43.9%, and the distribution of CYP2C19 genotypes was highest for CYP2C19(*1/*2) (43.0%), followed by CYP2C19 (*1/*1) (38.8%). The distribution of alleles *1, *2, *3, and *17 was 62.1, 32.5, 4.9, and 0.5%, respectively. A chi-squared test showed that the gene frequencies of alleles *2 and *3 were significantly higher in the clopidogrel-resistant group than in the clopidogrel-sensitive group (p < 0.001), and a Mann-Whitney U-test showed that high HCY levels were significantly correlated with clopidogrel resistance (p < 0.001). Multi-factor logistic regression analysis demonstrated that mutant heterozygous genotype [OR 2.893; 95% confidence interval (CI) 1.456-5.748; p = 0.002], mutant homozygous genotype (OR 4.741; 95% CI 1.828-12.298; p = 0.001), and high HCY levels (OR 1.209; 95% CI 1.072-1.362; p = 0.002) were significantly associated with clopidogrel resistance.According to our results, carrying the CYP2C19*2/*3 allele and high HCY levels are independent risk factors for clopidogrel resistance after clopidogrel therapy in patients with AIS. These two factors should be considered prior to clopidogrel administration.
         
            
 
                 
                
                    
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