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作 者:李新新[1,2] 钟诗龙[2] 李园[3] 韦素惠 张梦珍[2] 祁周措[2] 陈纪言[4] 劳海燕[2]
机构地区:[1]南方医科大学,广州市510515 [2]广东省人民医院(广东省医学科学院),广州市510080 [3]广东药学院,广州市510006 [4]广东省心血管病研究所,广州市510080
出 处:《实用医学杂志》2014年第7期1080-1083,共4页The Journal of Practical Medicine
基 金:国家自然科学基金项目(编号:81373486);广东省科技计划项目(编号:2012A030400062,2010B031600163)
摘 要:目的:探讨TIAM2功能性基因突变与冠心病患者经皮冠状动脉介入治疗(PCI)术后服用抗血小板药物氯吡格雷后出现出血事件的关联性。方法:从广东省人民医院顺序入选120例PCI术后接受氯吡格雷抗血小板治疗的中国汉族患者。应用PCR测序对PCI术后随访6个月的患者进行TIAM2启动子区基因分型检测。结果:随访6个月后,失访7例,实为113例,其中19例出现出血,94例未出现出血;合并糖尿病(OR=3.115)或是同时服用他汀类药物(OR=11.539)者出血风险可能较高,但无统计学差异(P<0.05);TIAM2启动子区有3个变异(c.3168+3116C>T、c.3168+3261A>G、c.3168+3596A>C),分为野生型、杂合型、纯合型,在出血患者中的概率分别为36.84%、52.63%、10.53%,存在一定的连锁状态,对氯吡格雷抗血小板治疗出现出血事件无显著的关联性(P>0.05)。结论:TIAM2功能性基因突变对氯吡格雷抗血小板治疗出现出血事件无显著影响。ObJective To explore the correlation of the TIAM2 functional gene mutations with the bleeding events in patients with coronary heart disease who undergone PCI and postoperative taken anti-platelet drug clopi- dogrel. Methods One hundred and twenty Chinese Han patients who had undergone PCI and postoperative taken anti-platelet drug clopidogrel were orderly enrolled from Guangdong General Hospital. Followed for 6 months after PCI, PCR sequencing was applied to test TIAM2 promoter region genotyping assay. Results After follow-up six months, 113 cases were remained lost of 7 cases,, including 19 cases with bleeding and 94 cases without bleed- ing; Bleeding risk in patients with diabetes mellitus (OR = 3.115) or taking statins (OR = 11.539), may be high, but there was no significant difference (P 〉 0.05) ; TIAM2 promoter region had three variants (c.3168 +3116C 〉T, c.3168+3261A〉G, c.3168+3596A〉C), including wild-type, heterozygous, and homozygous. The probability of pa- tients with bleeding were 36.84%, 52.63% and 10.53%, and there is a certain chain of state, but the genotype was not significantly correlated with bleeding events of clopidogrel antiplatelet therapy (P 〉 0.05). Conclusion Clopi- dogrel antiplatelet therapy bleeding events were not significantly correlated with TIAM2 functional gene mutation.
分 类 号:R541.4[医药卫生—心血管疾病]
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