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作 者:陈忠云[1] 李珊珊[1] 李婧[1] 徐志伟[1] 杨旭[1]
机构地区:[1]航天中心医院(北京大学航天临床医学院)神经内科,北京100049
出 处:《神经损伤与功能重建》2014年第2期111-114,共4页Neural Injury and Functional Reconstruction
摘 要:目的:探讨环氧合酶-2(COX-2)基因-1195 G<A多态性位点与缺血性脑卒中(IS)患者阿司匹林抵抗(AR)的相关性。方法:纳入中国北方汉族IS患者210例,根据血小板聚集率分为阿司匹林敏感(AS)组147例,非AS组63例。采用扩增阻碍突变系统(ARMS)结合TaqMan探针的实时荧光定量PCR方法检测-1195 G<A多态性。结果:-1195G<A位点基因型、显性模型分布频率在AS组及非AS组中差异均无统计学意义(P>0.05);非AS组中-1195G<A位点(GA+AA)基因型频率及A等位基因频率高于AS组,差异均有统计学意义(x^2=4.96,=0.03;x^2=5.50,P=0.02);多因素分析提示,与GG基因型相比,COX-2的-1195G<A位点(GA+AA)基因型发生AR可能性更大(OR=2.41,95%CI为1.09—5.37,P=0.03)。结论:COX-2基因—1195G〉A位点遗传变异与可能Is患者发生AR相关,可能是AR发生的一个遗传易感性位点。ObjectiveTo study the correlation between single nucleotide polymorphisms (SNPs) of-1195G〈A of cyclooxygenase-2 (COX-2) gene and Aspirin resistance (AR) in patients with ischemic stroke (IS). Methods:According to the rate of platelet aggregation, 210 northern Chinese Han patients with IS were divided into Aspirin sensitivity (AS) group (147 cases) and non-Asgroup [17 AR cases, and 46 Aspirin semi-resistance (ASR) cases] (n=63). The SNPs were detected by Amplification mutation system (ARMS) combined with TaqMan probe in a real-time PCR. Results:There were no significant differences in the genotype, allele, additive or recessive model frequencies of-1195G〈A polymorphisms between the 2 groups. The significant difference between (GA+AA) and GG genotype frequencies of-1195G〈A polymorphisms were observed in groups of AS and non-AS (P =0.03). For A allele of-1195G〈A, there was also a significant difference between the two groups (P =0.02). On multivariate analysis controlling for conventional vascular risk factors, the-1195 GA and AA genotypes were identified inde-pendently to be related with (ASR+AR) ( OR=2.41,:1.07-5.42, =0.03). Conclusion:-1195G〈A poly-morphism of COX-2 gene was associated with AR or ASR in patients with IS, which may be a genetic predisposi-tion to phenotypes of AR or ASR.
分 类 号:R741[医药卫生—神经病学与精神病学] R741.02[医药卫生—临床医学]
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