Unknown

Dataset Information

0

Pharmacogenetics in American Indian populations: analysis of CYP2D6, CYP3A4, CYP3A5, and CYP2C9 in the Confederated Salish and Kootenai Tribes.


ABSTRACT: OBJECTIVES:Cytochrome P450 enzymes play a dominant role in drug elimination and variation in these genes is a major source of interindividual differences in drug response. Little is known, however, about pharmacogenetic variation in American Indian and Alaska Native (AI/AN) populations. We have developed a partnership with the Confederated Salish and Kootenai Tribes (CSKT) in northwestern Montana to address this knowledge gap. METHODS:We resequenced CYP2D6 in 187 CSKT individuals and CYP3A4, CYP3A5, and CYP2C9 in 94 CSKT individuals. RESULTS:We identified 67 variants in CYP2D6, 15 in CYP3A4, 10 in CYP3A5, and 41 in CYP2C9. The most common CYP2D6 alleles were CYP2D6*4 and *41 (20.86 and 11.23%, respectively). CYP2D6*3, *5, *6, *9, *10, *17, *28, *33, *35, *49, *1xN, *2xN, and *4xN frequencies were less than 2%. CYP3A5*3, CYP3A4*1G, and *1B were detected with frequencies of 92.47, 26.81, and 2.20%, respectively. Allelic variation in CYP2C9 was low: CYP2C9*2 (5.17%) and *3 (2.69%). In general, allele frequencies in CYP2D6, CYP2C9, and CYP3A5 were similar to those observed in European Americans. There was, however, a marked divergence in CYP3A4 for the CYP3A4*1G allele. We also observed low levels of linkage between CYP3A4*1G and CYP3A5*1 in the CSKT. The combination of nonfunctional CYP3A5*3 and putative reduced function CYP3A4*1G alleles may predict diminished clearance of CYP3A substrates. CONCLUSION:These results highlight the importance of carrying out pharmacogenomic research in AI/AN populations and show that extrapolation from other populations is not appropriate. This information could help optimize drug therapy for the CSKT population.

SUBMITTER: Fohner A 

PROVIDER: S-EPMC3937472 | biostudies-literature | 2013 Aug

REPOSITORIES: biostudies-literature

altmetric image

Publications

Pharmacogenetics in American Indian populations: analysis of CYP2D6, CYP3A4, CYP3A5, and CYP2C9 in the Confederated Salish and Kootenai Tribes.

Fohner Alison A   Muzquiz LeeAnna I LI   Austin Melissa A MA   Gaedigk Andrea A   Gordon Adam A   Thornton Timothy T   Rieder Mark J MJ   Pershouse Mark A MA   Putnam Elizabeth A EA   Howlett Kevin K   Beatty Patrick P   Thummel Kenneth E KE   Woodahl Erica L EL  

Pharmacogenetics and genomics 20130801 8


<h4>Objectives</h4>Cytochrome P450 enzymes play a dominant role in drug elimination and variation in these genes is a major source of interindividual differences in drug response. Little is known, however, about pharmacogenetic variation in American Indian and Alaska Native (AI/AN) populations. We have developed a partnership with the Confederated Salish and Kootenai Tribes (CSKT) in northwestern Montana to address this knowledge gap.<h4>Methods</h4>We resequenced CYP2D6 in 187 CSKT individuals  ...[more]

Similar Datasets

| S-EPMC3093079 | biostudies-literature
| S-EPMC4278879 | biostudies-literature
| S-EPMC5872083 | biostudies-literature
| S-EPMC6938522 | biostudies-literature
| S-EPMC4160394 | biostudies-literature
| S-EPMC6082832 | biostudies-literature
| S-EPMC7094077 | biostudies-literature
| S-EPMC3874433 | biostudies-literature
| S-EPMC6925622 | biostudies-literature
| S-EPMC6510382 | biostudies-literature