首页> 外文OA文献 >Identification of New Alleles and the Determination of Alleles and Genotypes Frequencies at the CYP2D6 Gene in Emiratis
【2h】

Identification of New Alleles and the Determination of Alleles and Genotypes Frequencies at the CYP2D6 Gene in Emiratis

机译:拟南芥CYP2D6基因新等位基因的鉴定及等位基因和基因型频率的确定

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

CYP2D6 belongs to the cytochrome P450 superfamily of enzymes and plays an important role in the metabolism of 20–25% of clinically used drugs including antidepressants. It displays inter-individual and inter-ethnic variability in activity ranging from complete absence to excessive activity which causes adverse drug reactions and toxicity or therapy failure even at normal drug doses. This variability is due to genetic polymorphisms which form poor, intermediate, extensive or ultrarapid metaboliser phenotypes. This study aimed to determine CYP2D6 alleles and their frequencies in the United Arab Emirates (UAE) local population. CYP2D6 alleles and genotypes were determined by direct DNA sequencing in 151 Emiratis with the majority being psychiatric patients on antidepressants. Several new alleles have been identified and in total we identified seventeen alleles and 49 genotypes. CYP2D6*1 (wild type) and CYP2D6*2 alleles (extensive metaboliser phenotype) were found with frequencies of 39.1% and 12.2%, respectively. CYP2D6*41 (intermediate metaboliser) occurred in 15.2%. Homozygous CYP2D6*4 allele (poor metaboliser) was found with a frequency of 2% while homozygous and heterozygous CYP2D6*4 occurred with a frequency of 9%. CYP2D6*2xn, caused by gene duplication (ultrarapid metaboliser) had a frequency of 4.3%. CYP2D6 gene duplication/multiduplication occurred in 16% but only 11.2% who carried more than 2 active functional alleles were considered ultrarapid metabolisers. CYP2D6 gene deletion in one copy occurred in 7.5% of the study group. In conclusion, CYP2D6 gene locus is heterogeneous in the UAE national population and no significant differences have been identified between the psychiatric patients and controls.
机译:CYP2D6属于酶的细胞色素P450超家族,在20-25%的临床用药(包括抗抑郁药)的代谢中起重要作用。它显示出个体间和种族间活动的变异性,从完全缺乏到过度活动,甚至在正常药物剂量下也可能引起药物不良反应,毒性或治疗失败。这种可变性是由于遗传多态性所致,该遗传多态性形成不良的,中间的,广泛的或超快速的代谢者表型。这项研究旨在确定CYP2D6等位基因及其在阿拉伯联合酋长国(UAE)当地人口中的频率。 CYP2D6等位基因和基因型由151名Emiratis中的直接DNA测序确定,其中大多数是接受抗抑郁药治疗的精神病患者。已经鉴定了几个新的等位基因,我们总共鉴定了17个等位基因和49个基因型。发现CYP2D6 * 1(野生型)和CYP2D6 * 2等位基因(广泛代谢型)的频率分别为39.1%和12.2%。 CYP2D6 * 41(中间代谢者)的发生率为15.2%。发现纯合子CYP2D6 * 4等位基因(代谢不良)的频率为2%,而纯合和杂合CYP2D6 * 4等位基因的频率为9%。 CYP2D6 * 2xn由基因重复(超快速代谢)引起,频率为4.3%。 CYP2D6基因重复/多发发生在16%,但只有11.2%携带2个以上活跃的功能等位基因被认为是超快速代谢者。 CYP2D6基因缺失的一个拷贝在研究组的7.5%中发生。总之,CYP2D6基因位点在阿联酋国民中是异质的,在精神病患者和对照组之间没有发现显着差异。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号