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Exploration of association between EPHX1 and chronic obstructive pulmonary disease on the basis of combined data mining

机译:基于数据挖掘的ephε1和慢性阻塞性肺病的关联探讨

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Chronic obstructive pulmonary disease (COPD) is an important respiratory disease with high mortality. Although smoking is the major environmental risk factor for the development of COPD, only 10% of heavy smokers develop symptomatic disease, suggesting association between genetic susceptibilities and environmental influences. In recent years, as one of the most widely studied genes including tests for associations between a genetic variant and COPD, epoxide hydrolase 1 (EPHX1) was found to be involved in the metabolism of tobacco smoke, an important risk factor of COPD. However, genetic associations with COPD identified in studies on EPHX1 are controversial. To address this issue, except for performing the meta-analysis, which specially added our current study on two polymorphisms (T337C and A416G) of EPHX1, we performed combined data mining based on functional prediction algorithms of nonsynonymous single-nucleotide polymorphisms and gene-based variable threshold testing. Genetic variations in EPHX1 did not affect COPD in Caucasian and Eastern Asian population, which is supported by recent evidence. We found no association between EPHX1 and COPD; however, a minor effect of EPHX1 on COPD risk was not completely excluded; further replication studies with large samples are needed to confirm our findings.
机译:慢性阻塞性肺病(COPD)是具有高死亡率的重要呼吸系统疾病。虽然吸烟是COPD发展的主要环境风险因素,但只有10%的重重吸烟者发展症状性疾病,暗示遗传敏感性与环境影响之间的关联。近年来,作为最广泛研究的基因之一,包括遗传变异和COPD之间的关联试验,发现环氧化物水解酶1(EphX1)参与烟草烟雾的代谢,是COPD的重要危险因素。然而,在Ephx1研究中鉴定的遗传关联与ephx1中鉴定的copd是有争议的。为了解决这个问题,除了进行META分析,特别增加了我们目前对ephx1的两种多态性(T337C和A416G)的研究,我们基于非型单核苷酸多态性和基因的功能预测算法进行了组合的数据挖掘可变阈值测试。 Ephx1的遗传变异不会影响白种人和东亚人口中的COPD,这是最近证据的支持。我们发现Ephx1和COPD之间没有关联;但是,EPHX1对COPD风险的微小影响并未完全排除;需要使用大型样品进行进一步的复制研究来确认我们的研究结果。

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