Favela-Mendoza Alma Faviola, Rodríguez-Rodríguez Brenda Guadalupe, Rojas-Prado Eduardo, Chávez-Arreguin Mariana, Aguilar-Velázquez José Alonso, Martínez-Cortés Gabriela, Rangel-Villalobos Héctor
Instituto de Investigación en Genética Molecular, Centro Universitario de la Ciénega, Universidad de Guadalajara (CUCiénega-UdeG), Ocotlán, Jalisco, México.
Per Med. 2021 Sep;18(6):533-540. doi: 10.2217/pme-2020-0172. Epub 2021 Oct 22.
To evaluate the genetic distribution of the and variants in the gene in Mexican Mestizo (admixed) and Native American groups. We recruited 360 volunteers who were qPCR-genotyped with TaqMan probes. Allele and genotype frequencies are reported. Among the expected - haplotypes, T-A (42.35-58.47%) was the most prevalent which relates to the normal activity of the OATP1B1 transporter. This was followed by the T-G haplotype associated with further statin transport and cholesterol reduction (32.49-43.76%). Based on these gene variants, we confirmed that a minimum fraction of the Mexican study populations would be at risk from decreasing simvastatin transport and the development of statin-induced myopathy.
为评估墨西哥梅斯蒂索人(混血)和美洲原住民群体中基因的和变体的基因分布。我们招募了360名志愿者,用TaqMan探针进行qPCR基因分型。报告了等位基因和基因型频率。在预期的单倍型中,T-A(42.35-58.47%)最为普遍,这与OATP1B1转运蛋白的正常活性有关。其次是与进一步的他汀类药物转运和胆固醇降低相关的T-G单倍型(32.49-43.76%)。基于这些基因变体,我们证实墨西哥研究人群中至少有一部分人会因辛伐他汀转运减少和他汀类药物诱导的肌病发展而面临风险。