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Global variation in CYP2C8–CYP2C9 functional haplotypes
We have studied the global frequency distributions of 10 single nucleotide polymorphisms (SNPs) across 132 kb of CYP2C8 and CYP2C9 in ∼2500 individuals representing 45 populations. Five of the SNPs were in noncoding sequences; the other five involved the more common missense variants (four in CYP2C8...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2782405/ https://www.ncbi.nlm.nih.gov/pubmed/19381162 http://dx.doi.org/10.1038/tpj.2009.10 |
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author | Speed, William C Kang, Soonmo Peter Tuck, David P Harris, Lyndsay N Kidd, Kenneth K |
author_facet | Speed, William C Kang, Soonmo Peter Tuck, David P Harris, Lyndsay N Kidd, Kenneth K |
author_sort | Speed, William C |
collection | PubMed |
description | We have studied the global frequency distributions of 10 single nucleotide polymorphisms (SNPs) across 132 kb of CYP2C8 and CYP2C9 in ∼2500 individuals representing 45 populations. Five of the SNPs were in noncoding sequences; the other five involved the more common missense variants (four in CYP2C8, one in CYP2C9) that change amino acids in the gene products. One haplotype containing two CYP2C8 coding variants and one CYP2C9 coding variant reaches an average frequency of 10% in Europe; a set of haplotypes with a different CYP2C8 coding variant reaches 17% in Africa. In both cases these haplotypes are found in other regions of the world at <1%. This considerable geographic variation in haplotype frequencies impacts the interpretation of CYP2C8/CYP2C9 association studies, and has pharmacogenomic implications for drug interactions. |
format | Text |
id | pubmed-2782405 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-27824052010-02-01 Global variation in CYP2C8–CYP2C9 functional haplotypes Speed, William C Kang, Soonmo Peter Tuck, David P Harris, Lyndsay N Kidd, Kenneth K Pharmacogenomics J Original Articles We have studied the global frequency distributions of 10 single nucleotide polymorphisms (SNPs) across 132 kb of CYP2C8 and CYP2C9 in ∼2500 individuals representing 45 populations. Five of the SNPs were in noncoding sequences; the other five involved the more common missense variants (four in CYP2C8, one in CYP2C9) that change amino acids in the gene products. One haplotype containing two CYP2C8 coding variants and one CYP2C9 coding variant reaches an average frequency of 10% in Europe; a set of haplotypes with a different CYP2C8 coding variant reaches 17% in Africa. In both cases these haplotypes are found in other regions of the world at <1%. This considerable geographic variation in haplotype frequencies impacts the interpretation of CYP2C8/CYP2C9 association studies, and has pharmacogenomic implications for drug interactions. Nature Publishing Group 2009-04-21 2009-08 /pmc/articles/PMC2782405/ /pubmed/19381162 http://dx.doi.org/10.1038/tpj.2009.10 Text en Copyright 2009, Nature Publishing Group http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Original Articles Speed, William C Kang, Soonmo Peter Tuck, David P Harris, Lyndsay N Kidd, Kenneth K Global variation in CYP2C8–CYP2C9 functional haplotypes |
title | Global variation in CYP2C8–CYP2C9 functional haplotypes |
title_full | Global variation in CYP2C8–CYP2C9 functional haplotypes |
title_fullStr | Global variation in CYP2C8–CYP2C9 functional haplotypes |
title_full_unstemmed | Global variation in CYP2C8–CYP2C9 functional haplotypes |
title_short | Global variation in CYP2C8–CYP2C9 functional haplotypes |
title_sort | global variation in cyp2c8–cyp2c9 functional haplotypes |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2782405/ https://www.ncbi.nlm.nih.gov/pubmed/19381162 http://dx.doi.org/10.1038/tpj.2009.10 |
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