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厄瓜多尔人CYP3A5 3、CYP3A4 1B和MDR1 C3435T基因型分布情况。

CYP3A5 3, CYP3A4 1B and MDR1 C3435T genotype distributions in Ecuadorians.

作者信息

Sinués Blanca, Vicente Jorge, Fanlo Ana, Mayayo-Sinués Esteban, González-Andrade Fabricio, Sánchez-Q Dora, Martínez-Jarreta Begoña

机构信息

Department of Pharmacology, University of Zaragoza, Zaragoza, Spain.

出版信息

Dis Markers. 2008;24(6):325-31. doi: 10.1155/2008/750804.

Abstract

Polymorphisms in CYP3A genes, such as CYP3A5} and CYP3A4, as well as in the MDR1 gene, which encodes for P-glycoprotein, have been implicated as genetic markers in several disorders. Differences in the frequency distribution of the allelic variants CYP3A5 3, CYP3A4 1B, and MDR1 3435T have been demonstrated between distinct ethnic groups. In this study we examined the frequency of these allelic variants in 317 healthy Mestizo individuals from Ecuador and made comparisons with results reported in the literature. The genotypes were determined by PCR-RFLP. Allele and genotype differences were studied by chi-square test. The MDR1 T allele frequency was similar to that of Spaniard or Asian populations, which is consistent with the ethnic origin of Ecuadorian Mestizo individuals (Amerindian and Spaniard Caucasians). By contrast, the CYP3A5 3 allele frequency was significantly lower in Ecuadorians than in Spaniards and other white populations and higher than in Central Americans, Asians and blacks. CYP3A4 1B was more common in Ecuadorians than in Caucasian or Asian populations but less present than in blacks. The differences in the polymorphism found in this work should be considered in allele-disease association studies.

摘要

细胞色素P450 3A(CYP3A)基因多态性,如CYP3A5和CYP3A4,以及编码P-糖蛋白的多药耐药基因(MDR1)多态性,已被认为是多种疾病的遗传标志物。不同种族群体之间,等位基因变体CYP3A53、CYP3A41B和MDR1 3435T的频率分布存在差异。在本研究中,我们检测了317名来自厄瓜多尔的健康梅斯蒂索人这些等位基因变体的频率,并与文献报道的结果进行比较。通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)确定基因型。采用卡方检验研究等位基因和基因型差异。MDR1 T等位基因频率与西班牙人或亚洲人群相似,这与厄瓜多尔梅斯蒂索人的种族起源(美洲印第安人和西班牙白种人)一致。相比之下,厄瓜多尔人CYP3A53等位基因频率显著低于西班牙人和其他白种人群,高于中美洲人、亚洲人和黑人。CYP3A41B在厄瓜多尔人中比在白种人或亚洲人群中更常见,但比在黑人中少见。在等位基因与疾病关联研究中应考虑本研究发现的多态性差异。

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