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Significance of MDR1 gene C3435T polymorphism in predicting childhood refractory epilepsy

机译:MDR1基因C3435T多态性预测儿童难治性癫痫的意义

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The association between the MDR1 gene C3435T polymorphism and childhood intractable epilepsy remains controversial. In this study, we performed a meta-analysis to clarify this issue. We searched the PubMed, Medline, Embase and CNKI databases for studies published through October 2016 that evaluated the association between the MDR1 C3435T polymorphism and childhood refractory epilepsy. Eleven studies involving 863 cases in the group with drug-resistant epilepsy and 915 cases in the group with drug-responsive epilepsy were included in this systematic review and meta-analysis. The analysis showed that there was not a significant association of the MDR1 C3435T polymorphism overall with risk of drug-resistance. But the allelic association of MDR1 C3435T and the association of the MDR1 3435 CC genotype with risk of drug-resistance were significant among European population and a '>2010' group based on publication year subgroup analysis. The relationship between the MDR1 C3435T polymorphism and childhood refractory epilepsy needs further validation. (C) 2017 Elsevier B.V. All rights reserved.
机译:MDR1基因C3435T多态性和儿童顽固性癫痫之间的关联仍存在争议。在这项研究中,我们进行了一个荟萃分析以澄清这个问题。我们在2016年10月出版的研究中搜索了PubMed,Medline,Embase和CNKI数据库,评估了MDR1 C3435T多态性和儿童难治性癫痫之间的关联。涉及该组抗药性癫痫和915例患有药物响应癫痫的915例的1163例研究涉及该组织响应癫痫患者。该分析表明,MDR1 C3435T多态性的显着关联总体耐药风险。但MDR1 C3435T的等位基因协会和MDR1 3435 CC基因型与抗药性风险的关联是欧洲人口抗药性的显着性,基于出版年份亚组分析。 MDR1 C3435T多态性与儿童难治性癫痫之间的关系需要进一步验证。 (c)2017 Elsevier B.v.保留所有权利。

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