Yuan Xiao-Wen, Yuan Shi-Yun, Wu Guo-Xin, Wu Zhi-Xin, Guan Zi-Yun
Department of The Sixth Affiliated Hospital, School of Medicine, South China University of Technology, Foshan, People's Republic of China.
Department of Emergency Medicine, Department of Emergency Medicine, Foshan Hospital of Traditional Chinese Medicin, Foshan, People's Republic of China.
Hematology. 2022 Dec;27(1):1056-1061. doi: 10.1080/16078454.2022.2121899.
The gene is highly polymorphic, and is involved in the broad interindividual variability of the clinical efficacy of certain clinical medications, such as clopidogrel. However, data on the genotype in the Chinese population of the Foshan area of Guangdong Province are scarce. The purpose of this study was to determine genetic polymorphisms in patients in the Foshan area and to compare the genotype frequencies in different populations to determine the allele distribution pattern to identify the most appropriate prescription.
The gene was detected in 1231 patients on a gene chip platform, and the genotype frequencies of in Foshan populations from different populations were compared.
The frequencies of , and in the Foshan population were 63.89%, 30.46% and 5.65%, respectively. For the three metabolic types, the frequency associated with the rapid metabolism type () was 41.51 [95% confidence interval (CI) 40.11 to 42.91%]; that for the intermediate metabolism type () was 44.76% (95% CI 43.34 to 46.18) and that for the slow metabolism type ) was 13.73% (95% CI 12.75 to 14.71%). In the Foshan population, the frequencies of the and alleles were similar to those previously reported for Chinese and other Asian populations.
Our study is a report on the genetic basis of polymorphism in the Foshan population. Our results will potentially contribute to the improvement of pharmacotherapy effectiveness by providing personalized medicine for the Foshan population.
该基因具有高度多态性,且与某些临床药物(如氯吡格雷)临床疗效的广泛个体差异有关。然而,广东省佛山市地区中国人群中该基因的基因型数据稀缺。本研究的目的是确定佛山市地区患者的基因多态性,并比较不同人群中的基因型频率,以确定等位基因分布模式,从而确定最合适的处方。
在基因芯片平台上对1231例患者进行该基因检测,并比较佛山市不同人群中的基因型频率。
佛山市人群中该基因的、和基因型频率分别为63.89%、30.46%和5.65%。对于三种代谢类型,与快速代谢型()相关的频率为41.51[95%置信区间(CI)40.11至42.91%];中间代谢型()的频率为44.76%(95%CI 43.34至46.18),慢代谢型()的频率为13.73%(95%CI 12.75至14.71%)。在佛山市人群中,该基因和等位基因的频率与先前报道的中国及其他亚洲人群相似。
我们的研究是关于佛山市人群该基因多态性遗传基础的报告。我们的结果可能通过为佛山市人群提供个性化药物来促进药物治疗效果的改善。