首页|GP1BA、CYP2C19基因检测调整冠心病个体化抗血小板治疗策略及安全性评价

GP1BA、CYP2C19基因检测调整冠心病个体化抗血小板治疗策略及安全性评价

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探究通过GP1BA、CYP2C19基因多态性的检测调整冠心病个体化抗血小板治疗策略,评价抗血小板情况及安全性。前瞻性选取医院2021年11月至2022年12月收治的冠心病抗血小板治疗患者191例,进行GP1BA、CYP2C19基因检测,通过检测结果及血小板抑制率进行分组。按照基因分型及血小板抑制率分别制定个体化治疗策略,治疗90 d,观察两组性别、基础疾病、年龄、吸烟、BMI的差异,比较治疗策略调整前、调整治疗3个月后两组血小板计数、血小板抑制率、活化率、黏附率、疗效以及心源性死亡、出血、心绞痛、心肌梗死、血栓的等不良事件的发生率。通过结合AA/ADP抑制率以及CYP2C19、GP1BA基因型制定个体化治疗策略,结合AA/ADP抑制率以及 CYP2C19、GP1BA基因型分为观察组 95 例:AA/ADP 抑制率<20%、20%~50%、50%~75%、>95%;对照组96例:95%>AA/ADP抑制率>75%。在调整治疗策略前,观察组血小板计数(279。47±19。58)× 109/L明显高于对照组(198。36±12。92)× 109/L,P<0。05;治疗3个月后,两组血小板计数比较差异不显著,P>0。05。在调整治疗策略前,观察组血小板抑制率(29。62±1。69)%明显低于对照组(51。22±2。12)%,观察组血小板活化率(66。45±3。49)%、血小板黏附率(84。33±6。22)%明显高于对照组(42。51±2。39)%、(62。54± 4。31)%,P<0。05;治疗3个月后,两组血小板抑制率、活化率、黏附率比较差异不显著,P>0。05。调整治疗策略前,观察组总有效率(64。21%)显著低于对照组(91。67%),P<0。05;调整治疗策略后两组疗效差异不显著,P>0。05。观察组不良事件总发生率(5。26%)与对照组(4。17%)比较差异无统计学意义,P>0。05。通过对冠心病患者GP1BA、CYP2C19基因检测制定个体化治疗策略,获得了不错的效果,对调整冠心病个体化抗血小板治疗策略具有重要的临床意义,并且能够安全、可靠的调整抗血小板治疗策略,避免药量异常等导致不良心血管事件的发生。
GP1BA and CYP2C19 Gene Tests Adjust the Individualized Antiplatelet Therapy Strategy and Safety Evaluation of Coronary Heart Disease
To explore the adjustment of individualized antiplatelet therapy strategies for coronary heart disease through detection of GP1BA and CYP2C19 gene polymorphisms,and to evaluate the anti-platelet status and safety,a total of 191 patients with coronary heart disease receiving antiplatelet therapy in Hai'an People's Hospital from November 2021 to December 2022 were prospectively selected.GP1BA and CYP2C19 genes were detected and grouped according to the detection results and platelet inhibition rate.Individualized treatment strategies were developed according to genotyping and platelet inhibition rate,and the differences of gender,underlying diseases,age,smoking and BMI between the two groups were observed for 90 days.The platelet count,platelet inhibition rate,activation rate,adhesion rate,efficacy and the incidence of adverse events such as cardiac death,bleeding,angina pectoris,myocardial infarction and thrombosis were compared between the two groups before and after 3 months adjustment of treatment strategy.Individualized treatment strategies were developed by combining AA/ADP inhibition rate and CYP2C19 and GP1BA genotypes.Combined with the inhibition rate of AA/ADP and CYP2C19 and GP1BA genotypes,95 cases were divided into observation group:AA/ADP inhibition rate<20%,20%~50%,50%~75%,>95%,and 96 cases were enrolled in control group:95%>AA/ADP inhibition rate>75%.There were no significant differences in gender,underlying diseases(hypertension,diabetes,hyperlipidemia),age,smoking and BMI between the two groups(P>0.05).Before adjusting the treatment strategy,the platelet count of observation group(279.47± 19.58)× 109/L was significantly higher than that of control group(198.36±12.92)× 109/L,P<0.05;After 3 months of treat-ment,there was no significant difference in platelet count between the two groups(P>0.05).Before adjusting the treatment strategy,the platelet inhibition rate of observation group(29.62±1.69)%was significantly lower than that of control group(51.22± 2.12)%.The platelet activation rate(66.45±3.49)%and platelet adhesion rate(84.33±6.22)%in observation group were significantly higher than those in control group(42.51±2.39)%and(62.54±4.31)%,P<0.05.After 3 months of treatment,there were no significant differences in platelet inhibition rate,activation rate and adhesion rate between the two groups(P>0.05).Before the adjustment of treatment strategy,the total effective rate of the observation group(64.21%)was significantly lower than that of the control group(91.67%),P<0.05,and there was no significant difference between the two groups after the adjustment of treatment strategy,P>0.05.There was no significant difference in the total incidence of adverse events between the observation group(5.26%)and the control group(4.17%),P>0.05.Good results have been achieved through the development of individualized treatment strategies for the detection of GP1BA and CYP2C19 genes in patients with coronary heart disease,which has important clini-cal significance for the adjustment of individualized antiplatelet therapy strategies for coronary heart disease,and can safely and reliably adjust antiplatelet therapy strategies to avoid the occurrence of adverse cardiovascular events caused by abnormal drug dosage.

GP1 BACYP2C19Coronary heart diseaseIndividuationAntiplateletSecurity

谢飞、周虹、蔡伦、徐建华

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海安市人民医院药剂科,江苏海安 226600

宿迁市第一人民医院药学部,江苏宿迁 223800

GP1 BA CYP2C19 冠心病 个体化 抗血小板 安全性

南通市基础科学研究和社会民生科技计划项目南通市药学会-常州四药医院药学科研基金项目海安市人民医院院级科研项目

JCZ2022010ntyx2204202215

2024

药物生物技术
中国药科大学,中国医药科技出版社,中国药学会

药物生物技术

CSTPCD
影响因子:0.463
ISSN:1005-8915
年,卷(期):2024.31(2)
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