中华老年医学杂志
中華老年醫學雜誌
중화노년의학잡지
Chinese Journal of Geriatrics
2013年
5期
483-485
,共3页
朱琴%陈新宇%王国付%吕远栋
硃琴%陳新宇%王國付%呂遠棟
주금%진신우%왕국부%려원동
冠心病%细胞色素P450酶系统%多态性,单核苷酸
冠心病%細胞色素P450酶繫統%多態性,單覈苷痠
관심병%세포색소P450매계통%다태성,단핵감산
Coronary disease%Cytochrome P-450 enzyme system%Polymorphisms,single nucleotide
目的 探讨汉族冠状动脉粥样硬化性心脏病患者细胞色素P450氧化酶系统(CYP2C19)基因多态性与氯吡格雷药物临床疗效的关系. 方法 176例经皮冠状动脉介入治疗(PCI)术后,接受阿司匹林+氯吡格雷双联抗血小板治疗,运用PCR-RFLP方法进行CYP2C19*2,*3两种突变等位基因检测,根据等位基因功能缺失,分析CYP2C19不同代谢基因型与心血管终点事件的相关性. 结果 CYP2C19*2和*3的等位基因频率分别为34.38%和5.97%,慢代谢基因型(*2/*2,*2/*3,*3/*3)占14.20%.随访中11例患者急性冠脉综合征再发,1例出现脑梗死,4例患者出现支架内血栓,心血管终点事件的发生率为9.09%.慢代谢基因型组心血管终点事件的发生率为16.00%,与非慢代谢基因型组(7.95%)比较差异无统计学意义(x2=1.683,P=0.195).结论 中国汉族冠心病患者CYP2C19慢代谢基因型频率高于高加索人种,但心血管终点事件的发生率并无明显升高.
目的 探討漢族冠狀動脈粥樣硬化性心髒病患者細胞色素P450氧化酶繫統(CYP2C19)基因多態性與氯吡格雷藥物臨床療效的關繫. 方法 176例經皮冠狀動脈介入治療(PCI)術後,接受阿司匹林+氯吡格雷雙聯抗血小闆治療,運用PCR-RFLP方法進行CYP2C19*2,*3兩種突變等位基因檢測,根據等位基因功能缺失,分析CYP2C19不同代謝基因型與心血管終點事件的相關性. 結果 CYP2C19*2和*3的等位基因頻率分彆為34.38%和5.97%,慢代謝基因型(*2/*2,*2/*3,*3/*3)佔14.20%.隨訪中11例患者急性冠脈綜閤徵再髮,1例齣現腦梗死,4例患者齣現支架內血栓,心血管終點事件的髮生率為9.09%.慢代謝基因型組心血管終點事件的髮生率為16.00%,與非慢代謝基因型組(7.95%)比較差異無統計學意義(x2=1.683,P=0.195).結論 中國漢族冠心病患者CYP2C19慢代謝基因型頻率高于高加索人種,但心血管終點事件的髮生率併無明顯升高.
목적 탐토한족관상동맥죽양경화성심장병환자세포색소P450양화매계통(CYP2C19)기인다태성여록필격뢰약물림상료효적관계. 방법 176례경피관상동맥개입치료(PCI)술후,접수아사필림+록필격뢰쌍련항혈소판치료,운용PCR-RFLP방법진행CYP2C19*2,*3량충돌변등위기인검측,근거등위기인공능결실,분석CYP2C19불동대사기인형여심혈관종점사건적상관성. 결과 CYP2C19*2화*3적등위기인빈솔분별위34.38%화5.97%,만대사기인형(*2/*2,*2/*3,*3/*3)점14.20%.수방중11례환자급성관맥종합정재발,1례출현뇌경사,4례환자출현지가내혈전,심혈관종점사건적발생솔위9.09%.만대사기인형조심혈관종점사건적발생솔위16.00%,여비만대사기인형조(7.95%)비교차이무통계학의의(x2=1.683,P=0.195).결론 중국한족관심병환자CYP2C19만대사기인형빈솔고우고가색인충,단심혈관종점사건적발생솔병무명현승고.
Objective To investigate the association between CYP2C19 polymorphisms and efficacy of clopidogrel in Chinese Han patients with coronary atherosclerotic heart disease.Methods A total of 176 Chinese Han patients who underwent percutaneous coronary intervention and were treated with dual antiplatelet therapy with aspirin and clopidogrel were enrolled.Polymorphisms of CYP2C19 * 2,* 3 were measured by PCR-restriction fragment length polymorphism (PCR RFLP).The correlation between the genetic variants and cardiovascular events was analyzed.Results In the 176 patients,the allele frequencies of CYP2C19 * 2 and * 3 were 34.38% and 5.97% respectively,the percent of patients with poor metabolizer genotypes (* 2/* 2,* 2/* 3,* 3/* 3) was 14.20%.Among the 176 patients,11 patients reoccured acute coronary syndrome,1 patient suffered from stroke,and 4 patients had stent thrombosis.The incidence of cardiovascular events was 9.09 %.Thecumulative incidence of cardiovascular events had no significant differences between poor metabolizer genotype carriers and extensive and intermediate metabolizer genotype carriers (16.00% vs.7.95%,x2 =1.683,P=0.195).Conclusions The frequencies of CYP2C19 poor metabolizer genotypes are higher in Chinese Han population than in Caucasians,but the incidence of cardiovascular events in Chinese Han population is not increased.