Genetic variability in stroke patients: CYP2C19 polymorphisms unraveled
Peiyi Peng, Yingxiu Xiao, Xuehong Peng, Jianqiang Chen, Nuan Chen

TL;DR
This study examines how CYP2C19 gene variations are distributed in Han Chinese stroke patients and finds no significant correlation with age, sex, or stroke type.
Contribution
The study provides insights into CYP2C19 polymorphism distribution in Han Chinese stroke patients and suggests genotype-guided personalized treatment.
Findings
The most common CYP2C19 genotype in stroke patients was *1/*2, found in 42.44% of cases.
CYP2C19 genotypes, alleles, and metabolic types were not significantly associated with sex, age, or stroke type.
No independent risk factors for clopidogrel resistance were identified in the study population.
Abstract
To study the distribution characteristics of CYP2C19 polymorphisms in patients suffering from stroke in Han Chinese patients. PCR and DNA microarray chip technology were used to detect the CYP2C19 genotype of 549 patients with stroke, and the genotype, allele frequency and metabolic type of patients with different sexes, ages and types of infarctions and the independent risk factors for clopidogrel resistance were analyzed. Six genotypes were detected in these 549 patients. A total of 233 (42.44%) patients had the heterozygous allele *1/*2, which was the most prevalent, followed by the homozygous wild-type allele *1/*1 (191, 34.79%). A total of 30 (5.46%) patients possessed the heterozygous allele *1/*3, and 65 (11.84%) patients had the homozygous mutant allele *2/*2. Twenty-nine (5.28%) patients had the compound heterozygous mutant allele *2/*3, and only 1 patient had the homozygous…
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Taxonomy
TopicsAntiplatelet Therapy and Cardiovascular Diseases · Diabetes Treatment and Management · Lipoproteins and Cardiovascular Health
