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Pharmacokinetics/Genotype Associations for Major Cytochrome P450 Enzymes in Native and First‐ and Third‐generation Japanese Populations: Comparison With Korean, Chinese, and Caucasian Populations
Application of foreign clinical data across geographic regions can accelerate drug development. Drug disposition can be variable, and identification of factors influencing responsible pharmacokinetic/pharmacogenomic approaches could facilitate the universal application of foreign data and reduce the...
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Published in: | Clinical pharmacology and therapeutics 2008-09, Vol.84 (3), p.347-361 |
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creator | Myrand, SP Sekiguchi, K Man, MZ Lin, X Tzeng, R‐Y Teng, C‐H Hee, B Garrett, M Kikkawa, H Lin, C‐Y Eddy, SM Dostalik, J Mount, J Azuma, J Fujio, Y Jang, I‐J Shin, S‐G Bleavins, MR Williams, JA Paulauskis, JD Wilner, KD |
description | Application of foreign clinical data across geographic regions can accelerate drug development. Drug disposition can be variable, and identification of factors influencing responsible pharmacokinetic/pharmacogenomic approaches could facilitate the universal application of foreign data and reduce the total amount of phase III clinical trials evaluating risks in different populations. Our objective was to establish and compare genotype (major cytochrome P450 (CYP) enzymes)/phenotype associations for Japanese (native and first‐ and third‐generation Japanese living abroad), Caucasian, Chinese, and Korean populations using a standard drug panel. The mean metabolic ratios (MRs) for the four ethnic groups were similar except for a lower activity of CYP2D6 in Caucasians and CYP2C19 in Asians. Genotype, not ethnicity, impacted the MR for CYP2C9, CYP2C19, and CYP2D6; neither affected CYP1A2, CYP2E1, and CYP3A4/5 activities. We conclude that equivalent plasma drug concentrations and metabolic profiles can be expected for native Japanese, first‐ and third‐generation Japanese, Koreans, and Chinese for compounds handled through these six CYP enzymes.
Clinical Pharmacology & Therapeutics (2008); 84, 3, 347–361 doi:10.1038/sj.clpt.6100482 |
doi_str_mv | 10.1038/sj.clpt.6100482 |
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Clinical Pharmacology & Therapeutics (2008); 84, 3, 347–361 doi:10.1038/sj.clpt.6100482</description><identifier>ISSN: 0009-9236</identifier><identifier>EISSN: 1532-6535</identifier><identifier>DOI: 10.1038/sj.clpt.6100482</identifier><identifier>PMID: 18231117</identifier><identifier>CODEN: CLPTAT</identifier><language>eng</language><publisher>New York, NY: Nature Publishing</publisher><subject>Alleles ; Biological and medical sciences ; Clinical Trials, Phase III as Topic ; Cytochrome P-450 Enzyme System - blood ; Cytochrome P-450 Enzyme System - genetics ; Cytochrome P-450 Enzyme System - metabolism ; European Continental Ancestry Group - genetics ; Far East ; Genetics, Population ; Genotype ; Humans ; Japan ; Medical sciences ; Multicenter Studies as Topic ; Pharmacokinetics ; Pharmacology. Drug treatments</subject><ispartof>Clinical pharmacology and therapeutics, 2008-09, Vol.84 (3), p.347-361</ispartof><rights>2008 American Society for Clinical Pharmacology and Therapeutics</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3732-aaef0a89f95714f736f4777ed71626e62a73c2b81dbb3984b5389f0c4f42398c3</citedby><cites>FETCH-LOGICAL-c3732-aaef0a89f95714f736f4777ed71626e62a73c2b81dbb3984b5389f0c4f42398c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20605889$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18231117$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Myrand, SP</creatorcontrib><creatorcontrib>Sekiguchi, K</creatorcontrib><creatorcontrib>Man, MZ</creatorcontrib><creatorcontrib>Lin, X</creatorcontrib><creatorcontrib>Tzeng, R‐Y</creatorcontrib><creatorcontrib>Teng, C‐H</creatorcontrib><creatorcontrib>Hee, B</creatorcontrib><creatorcontrib>Garrett, M</creatorcontrib><creatorcontrib>Kikkawa, H</creatorcontrib><creatorcontrib>Lin, C‐Y</creatorcontrib><creatorcontrib>Eddy, SM</creatorcontrib><creatorcontrib>Dostalik, J</creatorcontrib><creatorcontrib>Mount, J</creatorcontrib><creatorcontrib>Azuma, J</creatorcontrib><creatorcontrib>Fujio, Y</creatorcontrib><creatorcontrib>Jang, I‐J</creatorcontrib><creatorcontrib>Shin, S‐G</creatorcontrib><creatorcontrib>Bleavins, MR</creatorcontrib><creatorcontrib>Williams, JA</creatorcontrib><creatorcontrib>Paulauskis, JD</creatorcontrib><creatorcontrib>Wilner, KD</creatorcontrib><title>Pharmacokinetics/Genotype Associations for Major Cytochrome P450 Enzymes in Native and First‐ and Third‐generation Japanese Populations: Comparison With Korean, Chinese, and Caucasian Populations</title><title>Clinical pharmacology and therapeutics</title><addtitle>Clin Pharmacol Ther</addtitle><description>Application of foreign clinical data across geographic regions can accelerate drug development. Drug disposition can be variable, and identification of factors influencing responsible pharmacokinetic/pharmacogenomic approaches could facilitate the universal application of foreign data and reduce the total amount of phase III clinical trials evaluating risks in different populations. Our objective was to establish and compare genotype (major cytochrome P450 (CYP) enzymes)/phenotype associations for Japanese (native and first‐ and third‐generation Japanese living abroad), Caucasian, Chinese, and Korean populations using a standard drug panel. The mean metabolic ratios (MRs) for the four ethnic groups were similar except for a lower activity of CYP2D6 in Caucasians and CYP2C19 in Asians. Genotype, not ethnicity, impacted the MR for CYP2C9, CYP2C19, and CYP2D6; neither affected CYP1A2, CYP2E1, and CYP3A4/5 activities. We conclude that equivalent plasma drug concentrations and metabolic profiles can be expected for native Japanese, first‐ and third‐generation Japanese, Koreans, and Chinese for compounds handled through these six CYP enzymes.
Clinical Pharmacology & Therapeutics (2008); 84, 3, 347–361 doi:10.1038/sj.clpt.6100482</description><subject>Alleles</subject><subject>Biological and medical sciences</subject><subject>Clinical Trials, Phase III as Topic</subject><subject>Cytochrome P-450 Enzyme System - blood</subject><subject>Cytochrome P-450 Enzyme System - genetics</subject><subject>Cytochrome P-450 Enzyme System - metabolism</subject><subject>European Continental Ancestry Group - genetics</subject><subject>Far East</subject><subject>Genetics, Population</subject><subject>Genotype</subject><subject>Humans</subject><subject>Japan</subject><subject>Medical sciences</subject><subject>Multicenter Studies as Topic</subject><subject>Pharmacokinetics</subject><subject>Pharmacology. 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Drug disposition can be variable, and identification of factors influencing responsible pharmacokinetic/pharmacogenomic approaches could facilitate the universal application of foreign data and reduce the total amount of phase III clinical trials evaluating risks in different populations. Our objective was to establish and compare genotype (major cytochrome P450 (CYP) enzymes)/phenotype associations for Japanese (native and first‐ and third‐generation Japanese living abroad), Caucasian, Chinese, and Korean populations using a standard drug panel. The mean metabolic ratios (MRs) for the four ethnic groups were similar except for a lower activity of CYP2D6 in Caucasians and CYP2C19 in Asians. Genotype, not ethnicity, impacted the MR for CYP2C9, CYP2C19, and CYP2D6; neither affected CYP1A2, CYP2E1, and CYP3A4/5 activities. We conclude that equivalent plasma drug concentrations and metabolic profiles can be expected for native Japanese, first‐ and third‐generation Japanese, Koreans, and Chinese for compounds handled through these six CYP enzymes.
Clinical Pharmacology & Therapeutics (2008); 84, 3, 347–361 doi:10.1038/sj.clpt.6100482</abstract><cop>New York, NY</cop><pub>Nature Publishing</pub><pmid>18231117</pmid><doi>10.1038/sj.clpt.6100482</doi><tpages>15</tpages></addata></record> |
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subjects | Alleles Biological and medical sciences Clinical Trials, Phase III as Topic Cytochrome P-450 Enzyme System - blood Cytochrome P-450 Enzyme System - genetics Cytochrome P-450 Enzyme System - metabolism European Continental Ancestry Group - genetics Far East Genetics, Population Genotype Humans Japan Medical sciences Multicenter Studies as Topic Pharmacokinetics Pharmacology. Drug treatments |
title | Pharmacokinetics/Genotype Associations for Major Cytochrome P450 Enzymes in Native and First‐ and Third‐generation Japanese Populations: Comparison With Korean, Chinese, and Caucasian Populations |
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