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High prevalence of CYP2C19*2 allele in Roma samples: study on Roma and Hungarian population samples with review of the literature

机译:CYP2C19 * 2等位基因在罗姆人样本中的高患病率:对罗姆人和匈牙利人口样本的研究并文献复习

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The purpose of our study was to characterise the CYP2C19*2 and CYP2C19*3 alleles in healthy Roma and Hungarian populations. DNA of 500 Roma and 370 Hungarian subjects were genotyped for CYP2C19*2 (G681A, rs4244285) and CYP2C19*3 (G636A, rs4986893) by PCR-RFLP assay and direct sequencing. Significant differences were found comparing the Roma and Hungarian populations in CYP2C19 681 GG (63.6 vs. 75.9 %), GA (31.8 vs. 23.0 %), AA (4.6 vs. 1.1 %), GA+AA (36.4 vs. 24.1 %) and A allele frequencies (0.205 vs. 0.125) (p < 0.004). Striking differences were found between Roma and Hungarian samples in CYP2C19*1 (79.5 vs. 87.4 %) and CYP2C19*2 (20.5 vs. 12.6 %) alleles, respectively (p < 0.001). None of the subjects was found to carry the CYP2C19*3 allele. Frequencies of the intermedier metabolizer phenotype defined by the *1/*2 genotype (0.318 vs. 0.230, p < 0.005) and poor metabolizer predicted by the *2/*2 genotype (0.046 vs. 0.011, p < 0.005) was significantly higher in Roma than in Hungarians, respectively. Genotype distribution of the Roma population was similar to those of the population of North India, however, a major difference was found in the frequency of the CYP2C19*2 allele, which is likely a result of admixture with European lineages. In conclusion, the frequencies of the CYP2C19 alleles, genotypes and corresponding extensive, intermediate and poor metabolizer phenotypes studied here in the Hungarian population are similar to those of other European Caucasian populations, but display clear differences when compared to the Roma population.
机译:我们的研究目的是鉴定健康的罗姆人和匈牙利人中的CYP2C19 * 2和CYP2C19 * 3等位基因。通过PCR-RFLP分析和直接测序对CYP2C19 * 2(G681A,rs4244285)和CYP2C19 * 3(G636A,rs4986893)的500名罗马人和370名匈牙利受试者的DNA进行基因分型。比较CYP2C19 681 GG(63.6 vs. 75.9%),GA(31.8 vs. 23.0%),AA(4.6 vs. 1.1%),GA + AA(36.4 vs.24.1%)的罗姆人和匈牙利人群体时发现了显着差异。和等位基因频率(0.205与0.125)(p <0.004)。在CYP2C19 * 1(79.5 vs. 87.4%)和CYP2C19 * 2(20.5 vs. 12.6%)等位基因的罗马和匈牙利样本之间发现了显着差异(p <0.001)。没有发现受试者携带CYP2C19 * 3等位基因。 * 1 / * 2基因型定义的中间代谢者表型的频率(0.318 vs. 0.230,p <0.005)和* 2 / * 2基因型定义的代谢不良者的频率(0.046 vs. 0.011,p <0.005)明显更高罗姆人比匈牙利人分别多。 Roma人群的基因型分布与北印度人群相似,但是,CYP2C19 * 2等位基因的频率存在主要差异,这可能是与欧洲血统混合的结果。总之,在匈牙利人群中研究的CYP2C19等位基因频率,基因型以及相应的广泛,中度和弱代谢者表型的频率与其他欧洲白种人人群的频率相似,但与罗姆人群相比显示出明显的差异。

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