cris.boxmetadata.label.title
Metabolizer phenotype prediction in different Peruvian ethnic groups through CYP2C9 polymorphisms
cris.boxmetadata.label.dateissued
01 browse.startsWith.months.june 2021
cris.boxmetadata.label.accesslevel
metadata only access
cris.boxmetadata.label.resourcetype
journal article
cris.boxmetadata.label.authors
Ayala E.V.
Chevarría Arriaga M.
Coelho E.B.
SALAZAR GRANARA, ALBERTO ALCIBIADES
cris.boxmetadata.label.publisher
De Gruyter Open Ltd
cris.boxmetadata.label.abstract
The CYP2C9 gene have three common alleles, CYP2C9∗1, CYP2C9∗2 and CYP2C9∗3, associated with different homozygous (∗1/∗1, ∗2/∗2 and ∗3/∗3) and heterozygous (∗1/∗2 and ∗1/∗3) genotypes, which in turn are related to extensive (gEM), intermediate (gIM) and poor (gPM) metabolizers. Likewise, the inter-ethnic variability was intimately associated with different drug metabolism. Therefore, the aim of the present study was predict the metabolizer phenotypes in different Peruvian ethnic groups from lowland (<2,500 m) and highland (>2,500 m). TaqMan genotyping assays were performed in a group of 174 healthy unrelated Peruvian individuals. In this study, the allelic comparison between the three eco-regions showed that the CYP2C9∗1 was the most common in Andean (96.32%); the ∗2 was the most frequent in Coast (7.45%, p<0.05). Regarding the ∗3 was the most common in Amazonian (6.25%, p<0.05). In a corroborative manner, the gEM was the most common in Andean (94.74%), the gIM in Coast (17.02%) and gPM in Amazonian (6.25%) populations. Our study provides a valuable source of information about to metabolizer phenotype drugs in different Peruvian ethnic groups. In this way, it could be established suitable genetic-dosage medicaments for various common diseases in these heterogenetic populations.
cris.boxmetadata.label.citationstartpage
113
cris.boxmetadata.label.citationendpage
121
cris.boxmetadata.label.volume
36
cris.boxmetadata.label.issue
2
cris.boxmetadata.label.language
English
cris.boxmetadata.label.ocdeknowledgeArea
Genética humana
cris.boxmetadata.label.subjects
cris.boxmetadata.label.doi
cris.boxmetadata.label.scopusidentifier
2-s2.0-85104576030
cris.boxmetadata.label.pubmedidentifier
cris.boxmetadata.label.source
Drug Metabolism and Personalized Therapy
cris.boxmetadata.label.containerissn
23638907
cris.boxmetadata.label.sponsor
Research funding: The study was supported by Universidad de San Martín de Porres - Facultad de Medicina Humana & Universidade de São Paulo - Faculdade de Medicina de Ribeirão Preto.
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