Griman Pedro, Moran Yeinmy, Valero Gabriela, Loreto Mariana, Borjas Lisbeth, Chiurillo Miguel A
Laboratorio de Genética Molecular Dr Jorge Yunis-Turbay, Decanato de Ciencias de la Salud, Universidad Centroccidental Lisandro Alvarado, Barquisimeto 3001, Venezuela.
Ann Hum Biol. 2012 Mar;39(2):137-42. doi: 10.3109/03014460.2012.656703.
Differences in genes encoding enzymes involved in the biotransformation of a large number of compounds, such as CYP2D6, are related to inter-individual and inter-ethnic variability in the metabolism of many drugs, which have also been linked to susceptibility to cancer and other health outcomes. Therefore, populations are likely to benefit from inclusion in pharmacogenetic research studies.
To determine the frequency of functionally important allele variants of CYP2D6 gene in a sample of an Urban/admixed and five Amerindian Venezuelan populations.
DNA of 328 unrelated volunteers was analysed for the presence of CYP2D6 *2, *3, *4, *5, *6 and *10 variants.
The frequency in the Urban/admixed population for *2, *3, *4, *5, *6 and *10 alleles was 37.9%, 0%, 13.4%, 2.0%, 1.2% and 4.0%, respectively. In the Bari population, the prevalence of *4 allele associated with decreased enzyme activity was observed in 42.5%, whereas the poor metabolizer genotype *4/*4 was found in 25%. In the Panare, Pemon, Warao and Wayuu populations the *4 allele was found in 5.4%, 2.5%, 1.7% and 4.2%, respectively. The *10 allele frequency found in Amerindians (0.0-6.3%) was lower than reported for Asians.
The results are consistent with the known genetic admixture origin of most Venezuela populations. Nevertheless, the observed significant differences among Amerindians highlight the need for pharmacogenetic studies taking into account biogeographical and anthropological considerations.
编码参与大量化合物生物转化的酶的基因差异,如CYP2D6,与许多药物代谢的个体间和种族间变异性有关,这也与癌症易感性和其他健康结果相关。因此,人群可能会从纳入药物遗传学研究中受益。
确定城市/混合人群以及五个委内瑞拉美洲印第安人群样本中CYP2D6基因功能重要等位基因变体的频率。
分析328名无关志愿者的DNA中CYP2D6 *2、*3、*4、*5、6和10变体的存在情况。
城市/混合人群中*2、*3、4、5、6和10等位基因的频率分别为37.9%、0%、13.4%、2.0%、1.2%和4.0%。在巴里人群中,与酶活性降低相关的4等位基因的患病率为42.5%,而代谢不良基因型4/*4的比例为25%。在帕纳雷、佩蒙、瓦劳和瓦尤人群中,4等位基因的比例分别为5.4%、2.5%、1.7%和4.2%。美洲印第安人中发现的10等位基因频率(0.0 - 6.3%)低于亚洲人报道的频率。
结果与大多数委内瑞拉人群已知的遗传混合起源一致。然而,美洲印第安人之间观察到的显著差异凸显了在药物遗传学研究中考虑生物地理和人类学因素的必要性。