4.4 Article

Influence of CYP2D6 Deletion, Multiplication,-1584C -> G, 31G -> A and 2988G -> A Gene Polymorphisms on Dextromethorphan Metabolism among Mexican Tepehuanos and Mestizos

Journal

PHARMACOLOGY
Volume 86, Issue 1, Pages 30-36

Publisher

KARGER
DOI: 10.1159/000314334

Keywords

CYP2D6 polymorphism; Mexican Tepehuanos; Dextromethorphan metabolism; Allele frequency

Funding

  1. CONACYT-Mexico [60694]
  2. AEXCID Cooperacion Extreme a of Junta de Extremadura [9IA006]
  3. Red Iberoamericana de Farmacogenetica y Farmacogenomica [CYTED206RT0290]
  4. Instituto de Salud Carlos III-FIS and the European Union (FEEDER) [CP/06/00030]

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The aim of this study was to explain the variability of CYP2D6 activity by the identification of CYP2D6 deletion and multiplications, and the single- nucleotide polymorphisms ( SNPs) - 1584C -> G, 31G -> A and 2988G -> A in Mexican Mestizo and Tepehuano subjects. One hundred twelve Mestizos and 99 Tepehuano Amerindians were studied, who were previously phenotyped with dextromethorphan. The frequencies of CYP2D6*2A [-1584C -> G] and *35 [-1584C -> G, 31G -> A] were 10.7 and 4.1%, respectively, in Mestizos, which is evidently a trend towards an extensive metabolism in carriers of the -1584G change. In Tepehuanos, *2A was identified with a frequency of 20%, and the allele *35 was not found. The frequencies of CYP2D6* 5 ( deletion) and *41 [2988G -> A] were 1.3 and 2.2% in Mestizos and 0.5 and 1% in Tepehuanos, respectively. The SNP 2988A was found to be significantly related with the intermediate metabolizer phenotype in Mestizos ( R = 0.309; n = 88; p = 0.006). The multiplications had frequencies of 4.1% in Mestizos and 1.5% in Tepehuanos. Only in the Mestizos did the presence of multiplications significantly decrease the DM/DX (dextromethorphan/dextrorphan) values (R = 0.273; n = 88; p = 0.016). The polymorphisms studied had different frequencies between Tepehuanos and Mestizos (p < 0.001); however, in the Tepehuano group these had a low influence on their phenotypic expression. It helps to understand the genotype-phenotype relationships of CYP2D6 in our studied populations. Copyright (C) 2010 S. Karger AG, Basel

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