CYP2D6 allele frequencies in Korean population, comparison with East Asian, Caucasian and African populations, and the comparison of metabolic activity of CYP2D6 genotypes

Cytochrome P450 (CYP) 2D6 is present in less than about 2% of all CYP enzymes in the liver, but it is involved in the metabolism of about 25% of currently used drugs. CYP2D6 is the most polymorphic among the CYP enzymes. We determined alleles and genotypes of CYP2D6 in 3417 Koreans, compared the fre...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Archives of pharmacal research 2018-09, Vol.41 (9), p.921-930
Hauptverfasser: Byeon, Ji-Young, Kim, Young-Hoon, Lee, Choong-Min, Kim, Se-Hyung, Chae, Won-Ki, Jung, Eui-Hyun, Choi, Chang-Ik, Jang, Choon-Gon, Lee, Seok-Yong, Bae, Jung-Woo, Lee, Yun Jeong
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 930
container_issue 9
container_start_page 921
container_title Archives of pharmacal research
container_volume 41
creator Byeon, Ji-Young
Kim, Young-Hoon
Lee, Choong-Min
Kim, Se-Hyung
Chae, Won-Ki
Jung, Eui-Hyun
Choi, Chang-Ik
Jang, Choon-Gon
Lee, Seok-Yong
Bae, Jung-Woo
Lee, Yun Jeong
description Cytochrome P450 (CYP) 2D6 is present in less than about 2% of all CYP enzymes in the liver, but it is involved in the metabolism of about 25% of currently used drugs. CYP2D6 is the most polymorphic among the CYP enzymes. We determined alleles and genotypes of CYP2D6 in 3417 Koreans, compared the frequencies of CYP2D6 alleles with other populations, and observed the differences in pharmacokinetics of metoprolol, a prototype CYP2D6 substrate, depending on CYP2D6 genotype. A total of 3417 unrelated healthy subjects were recruited for the genotyping of CYP2D6 gene. Among them, 42 subjects with different CYP2D6 genotypes were enrolled in the pharmacokinetic study of metoprolol. The functional allele *1 and *2 were present in frequencies of 34.6 and 11.8%, respectively. In decreased functional alleles, *10 was the most frequent with 46.2% and *41 allele was present in 1.4%. The nonfunctional alleles *5 and *14 were present at 4.5 and 0.5% frequency, respectively. The *X  × N allele was present at a frequency of 1.0%. CYP2D6*1/*1 , *1/*2 and *2/*2 genotypes with normal enzyme activity were present in 12.1%, 8.6% and 1.4% of the subjects, respectively. CYP2D6*5/*5 , *5/*14 , and *14/*14 genotypes classified as poor metabolizer were only present in 4, 2, and 1 subjects, respectively. Mutant genotypes with frequencies of more than 1% were CYP2D6*1/*10 (32.0%), *10/*10 (22.3%), *2/*10 (11.7%), *5/*10 (3.7%), *1/*5 (2.5%), and *10/*41 (1.2%). The relative clearance of metoprolol in CYP2D6*1/*10 , *1/*5 , *10/*10 , *5/*10 , and *5/*5 genotypes were 69%, 57%, 24%, 14% and 9% of CYP2D6*wt/*wt genotype, respectively. These results will be very useful in establishing a strategy for precision medicine related to the genetic polymorphism of CYP2D6 .
doi_str_mv 10.1007/s12272-018-1075-6
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2101275530</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2101275530</sourcerecordid><originalsourceid>FETCH-LOGICAL-c344t-8a810188296f7b2bd04e5cfbdb2a8515dd3f973ba149f9d9725bf0b6f42545d63</originalsourceid><addsrcrecordid>eNp9kc1u1DAUhS0EotPCA7BBXrJowD-xnSxHQ6GISu0CFqws27FbV4kdbAc0z8RL4jADajesrnXPuZ-u7wHgFUZvMULiXcaECNIg3DUYCdbwJ2CDe8EbKjr-FGwQYbThhPcn4DTne4QoZ4w9BycU4R63HG3Ar923G_KeQzWOdrTQJft9scF4m6EP8HNMVgU4x3kZVfExnEMTp1kln2OAP325gxcqF7jNXlVtpxaj1idUYYBbl7x5NJ3P_wjlzj7ERAcnW5SOozdQmeJ_-LJfu8fVbm2IZT_b_AI8c2rM9uWxnoGvHy6-7C6bq-uPn3bbq8bQti1NpzpcT9KRnjuhiR5Qa5lxetBEdQyzYaCuF1Qr3PauH3pBmHZIc9cS1rKB0zPw5sCdU6zXyEVOPhs7jirYuGRJKp4IxiiqVnywmhRzTtbJOflJpb3ESK4ZyUNGsi4k14zkin99xC96ssO_ib-hVAM5GHKVwq1N8j4uKdQv_4f6G98wniw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2101275530</pqid></control><display><type>article</type><title>CYP2D6 allele frequencies in Korean population, comparison with East Asian, Caucasian and African populations, and the comparison of metabolic activity of CYP2D6 genotypes</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>Byeon, Ji-Young ; Kim, Young-Hoon ; Lee, Choong-Min ; Kim, Se-Hyung ; Chae, Won-Ki ; Jung, Eui-Hyun ; Choi, Chang-Ik ; Jang, Choon-Gon ; Lee, Seok-Yong ; Bae, Jung-Woo ; Lee, Yun Jeong</creator><creatorcontrib>Byeon, Ji-Young ; Kim, Young-Hoon ; Lee, Choong-Min ; Kim, Se-Hyung ; Chae, Won-Ki ; Jung, Eui-Hyun ; Choi, Chang-Ik ; Jang, Choon-Gon ; Lee, Seok-Yong ; Bae, Jung-Woo ; Lee, Yun Jeong</creatorcontrib><description>Cytochrome P450 (CYP) 2D6 is present in less than about 2% of all CYP enzymes in the liver, but it is involved in the metabolism of about 25% of currently used drugs. CYP2D6 is the most polymorphic among the CYP enzymes. We determined alleles and genotypes of CYP2D6 in 3417 Koreans, compared the frequencies of CYP2D6 alleles with other populations, and observed the differences in pharmacokinetics of metoprolol, a prototype CYP2D6 substrate, depending on CYP2D6 genotype. A total of 3417 unrelated healthy subjects were recruited for the genotyping of CYP2D6 gene. Among them, 42 subjects with different CYP2D6 genotypes were enrolled in the pharmacokinetic study of metoprolol. The functional allele *1 and *2 were present in frequencies of 34.6 and 11.8%, respectively. In decreased functional alleles, *10 was the most frequent with 46.2% and *41 allele was present in 1.4%. The nonfunctional alleles *5 and *14 were present at 4.5 and 0.5% frequency, respectively. The *X  × N allele was present at a frequency of 1.0%. CYP2D6*1/*1 , *1/*2 and *2/*2 genotypes with normal enzyme activity were present in 12.1%, 8.6% and 1.4% of the subjects, respectively. CYP2D6*5/*5 , *5/*14 , and *14/*14 genotypes classified as poor metabolizer were only present in 4, 2, and 1 subjects, respectively. Mutant genotypes with frequencies of more than 1% were CYP2D6*1/*10 (32.0%), *10/*10 (22.3%), *2/*10 (11.7%), *5/*10 (3.7%), *1/*5 (2.5%), and *10/*41 (1.2%). The relative clearance of metoprolol in CYP2D6*1/*10 , *1/*5 , *10/*10 , *5/*10 , and *5/*5 genotypes were 69%, 57%, 24%, 14% and 9% of CYP2D6*wt/*wt genotype, respectively. These results will be very useful in establishing a strategy for precision medicine related to the genetic polymorphism of CYP2D6 .</description><identifier>ISSN: 0253-6269</identifier><identifier>EISSN: 1976-3786</identifier><identifier>DOI: 10.1007/s12272-018-1075-6</identifier><identifier>PMID: 30191460</identifier><language>eng</language><publisher>Seoul: Pharmaceutical Society of Korea</publisher><subject>African Continental Ancestry Group - genetics ; Asian Continental Ancestry Group - genetics ; Cytochrome P-450 CYP2D6 - genetics ; Cytochrome P-450 CYP2D6 - metabolism ; European Continental Ancestry Group - genetics ; Gene Frequency - genetics ; Genotype ; Humans ; Medicine ; Pharmacology/Toxicology ; Pharmacy ; Republic of Korea ; Research Article</subject><ispartof>Archives of pharmacal research, 2018-09, Vol.41 (9), p.921-930</ispartof><rights>The Pharmaceutical Society of Korea 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c344t-8a810188296f7b2bd04e5cfbdb2a8515dd3f973ba149f9d9725bf0b6f42545d63</citedby><cites>FETCH-LOGICAL-c344t-8a810188296f7b2bd04e5cfbdb2a8515dd3f973ba149f9d9725bf0b6f42545d63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12272-018-1075-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12272-018-1075-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27923,27924,41487,42556,51318</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30191460$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Byeon, Ji-Young</creatorcontrib><creatorcontrib>Kim, Young-Hoon</creatorcontrib><creatorcontrib>Lee, Choong-Min</creatorcontrib><creatorcontrib>Kim, Se-Hyung</creatorcontrib><creatorcontrib>Chae, Won-Ki</creatorcontrib><creatorcontrib>Jung, Eui-Hyun</creatorcontrib><creatorcontrib>Choi, Chang-Ik</creatorcontrib><creatorcontrib>Jang, Choon-Gon</creatorcontrib><creatorcontrib>Lee, Seok-Yong</creatorcontrib><creatorcontrib>Bae, Jung-Woo</creatorcontrib><creatorcontrib>Lee, Yun Jeong</creatorcontrib><title>CYP2D6 allele frequencies in Korean population, comparison with East Asian, Caucasian and African populations, and the comparison of metabolic activity of CYP2D6 genotypes</title><title>Archives of pharmacal research</title><addtitle>Arch. Pharm. Res</addtitle><addtitle>Arch Pharm Res</addtitle><description>Cytochrome P450 (CYP) 2D6 is present in less than about 2% of all CYP enzymes in the liver, but it is involved in the metabolism of about 25% of currently used drugs. CYP2D6 is the most polymorphic among the CYP enzymes. We determined alleles and genotypes of CYP2D6 in 3417 Koreans, compared the frequencies of CYP2D6 alleles with other populations, and observed the differences in pharmacokinetics of metoprolol, a prototype CYP2D6 substrate, depending on CYP2D6 genotype. A total of 3417 unrelated healthy subjects were recruited for the genotyping of CYP2D6 gene. Among them, 42 subjects with different CYP2D6 genotypes were enrolled in the pharmacokinetic study of metoprolol. The functional allele *1 and *2 were present in frequencies of 34.6 and 11.8%, respectively. In decreased functional alleles, *10 was the most frequent with 46.2% and *41 allele was present in 1.4%. The nonfunctional alleles *5 and *14 were present at 4.5 and 0.5% frequency, respectively. The *X  × N allele was present at a frequency of 1.0%. CYP2D6*1/*1 , *1/*2 and *2/*2 genotypes with normal enzyme activity were present in 12.1%, 8.6% and 1.4% of the subjects, respectively. CYP2D6*5/*5 , *5/*14 , and *14/*14 genotypes classified as poor metabolizer were only present in 4, 2, and 1 subjects, respectively. Mutant genotypes with frequencies of more than 1% were CYP2D6*1/*10 (32.0%), *10/*10 (22.3%), *2/*10 (11.7%), *5/*10 (3.7%), *1/*5 (2.5%), and *10/*41 (1.2%). The relative clearance of metoprolol in CYP2D6*1/*10 , *1/*5 , *10/*10 , *5/*10 , and *5/*5 genotypes were 69%, 57%, 24%, 14% and 9% of CYP2D6*wt/*wt genotype, respectively. These results will be very useful in establishing a strategy for precision medicine related to the genetic polymorphism of CYP2D6 .</description><subject>African Continental Ancestry Group - genetics</subject><subject>Asian Continental Ancestry Group - genetics</subject><subject>Cytochrome P-450 CYP2D6 - genetics</subject><subject>Cytochrome P-450 CYP2D6 - metabolism</subject><subject>European Continental Ancestry Group - genetics</subject><subject>Gene Frequency - genetics</subject><subject>Genotype</subject><subject>Humans</subject><subject>Medicine</subject><subject>Pharmacology/Toxicology</subject><subject>Pharmacy</subject><subject>Republic of Korea</subject><subject>Research Article</subject><issn>0253-6269</issn><issn>1976-3786</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc1u1DAUhS0EotPCA7BBXrJowD-xnSxHQ6GISu0CFqws27FbV4kdbAc0z8RL4jADajesrnXPuZ-u7wHgFUZvMULiXcaECNIg3DUYCdbwJ2CDe8EbKjr-FGwQYbThhPcn4DTne4QoZ4w9BycU4R63HG3Ar923G_KeQzWOdrTQJft9scF4m6EP8HNMVgU4x3kZVfExnEMTp1kln2OAP325gxcqF7jNXlVtpxaj1idUYYBbl7x5NJ3P_wjlzj7ERAcnW5SOozdQmeJ_-LJfu8fVbm2IZT_b_AI8c2rM9uWxnoGvHy6-7C6bq-uPn3bbq8bQti1NpzpcT9KRnjuhiR5Qa5lxetBEdQyzYaCuF1Qr3PauH3pBmHZIc9cS1rKB0zPw5sCdU6zXyEVOPhs7jirYuGRJKp4IxiiqVnywmhRzTtbJOflJpb3ESK4ZyUNGsi4k14zkin99xC96ssO_ib-hVAM5GHKVwq1N8j4uKdQv_4f6G98wniw</recordid><startdate>20180901</startdate><enddate>20180901</enddate><creator>Byeon, Ji-Young</creator><creator>Kim, Young-Hoon</creator><creator>Lee, Choong-Min</creator><creator>Kim, Se-Hyung</creator><creator>Chae, Won-Ki</creator><creator>Jung, Eui-Hyun</creator><creator>Choi, Chang-Ik</creator><creator>Jang, Choon-Gon</creator><creator>Lee, Seok-Yong</creator><creator>Bae, Jung-Woo</creator><creator>Lee, Yun Jeong</creator><general>Pharmaceutical Society of Korea</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20180901</creationdate><title>CYP2D6 allele frequencies in Korean population, comparison with East Asian, Caucasian and African populations, and the comparison of metabolic activity of CYP2D6 genotypes</title><author>Byeon, Ji-Young ; Kim, Young-Hoon ; Lee, Choong-Min ; Kim, Se-Hyung ; Chae, Won-Ki ; Jung, Eui-Hyun ; Choi, Chang-Ik ; Jang, Choon-Gon ; Lee, Seok-Yong ; Bae, Jung-Woo ; Lee, Yun Jeong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c344t-8a810188296f7b2bd04e5cfbdb2a8515dd3f973ba149f9d9725bf0b6f42545d63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>African Continental Ancestry Group - genetics</topic><topic>Asian Continental Ancestry Group - genetics</topic><topic>Cytochrome P-450 CYP2D6 - genetics</topic><topic>Cytochrome P-450 CYP2D6 - metabolism</topic><topic>European Continental Ancestry Group - genetics</topic><topic>Gene Frequency - genetics</topic><topic>Genotype</topic><topic>Humans</topic><topic>Medicine</topic><topic>Pharmacology/Toxicology</topic><topic>Pharmacy</topic><topic>Republic of Korea</topic><topic>Research Article</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Byeon, Ji-Young</creatorcontrib><creatorcontrib>Kim, Young-Hoon</creatorcontrib><creatorcontrib>Lee, Choong-Min</creatorcontrib><creatorcontrib>Kim, Se-Hyung</creatorcontrib><creatorcontrib>Chae, Won-Ki</creatorcontrib><creatorcontrib>Jung, Eui-Hyun</creatorcontrib><creatorcontrib>Choi, Chang-Ik</creatorcontrib><creatorcontrib>Jang, Choon-Gon</creatorcontrib><creatorcontrib>Lee, Seok-Yong</creatorcontrib><creatorcontrib>Bae, Jung-Woo</creatorcontrib><creatorcontrib>Lee, Yun Jeong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Archives of pharmacal research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Byeon, Ji-Young</au><au>Kim, Young-Hoon</au><au>Lee, Choong-Min</au><au>Kim, Se-Hyung</au><au>Chae, Won-Ki</au><au>Jung, Eui-Hyun</au><au>Choi, Chang-Ik</au><au>Jang, Choon-Gon</au><au>Lee, Seok-Yong</au><au>Bae, Jung-Woo</au><au>Lee, Yun Jeong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CYP2D6 allele frequencies in Korean population, comparison with East Asian, Caucasian and African populations, and the comparison of metabolic activity of CYP2D6 genotypes</atitle><jtitle>Archives of pharmacal research</jtitle><stitle>Arch. Pharm. Res</stitle><addtitle>Arch Pharm Res</addtitle><date>2018-09-01</date><risdate>2018</risdate><volume>41</volume><issue>9</issue><spage>921</spage><epage>930</epage><pages>921-930</pages><issn>0253-6269</issn><eissn>1976-3786</eissn><abstract>Cytochrome P450 (CYP) 2D6 is present in less than about 2% of all CYP enzymes in the liver, but it is involved in the metabolism of about 25% of currently used drugs. CYP2D6 is the most polymorphic among the CYP enzymes. We determined alleles and genotypes of CYP2D6 in 3417 Koreans, compared the frequencies of CYP2D6 alleles with other populations, and observed the differences in pharmacokinetics of metoprolol, a prototype CYP2D6 substrate, depending on CYP2D6 genotype. A total of 3417 unrelated healthy subjects were recruited for the genotyping of CYP2D6 gene. Among them, 42 subjects with different CYP2D6 genotypes were enrolled in the pharmacokinetic study of metoprolol. The functional allele *1 and *2 were present in frequencies of 34.6 and 11.8%, respectively. In decreased functional alleles, *10 was the most frequent with 46.2% and *41 allele was present in 1.4%. The nonfunctional alleles *5 and *14 were present at 4.5 and 0.5% frequency, respectively. The *X  × N allele was present at a frequency of 1.0%. CYP2D6*1/*1 , *1/*2 and *2/*2 genotypes with normal enzyme activity were present in 12.1%, 8.6% and 1.4% of the subjects, respectively. CYP2D6*5/*5 , *5/*14 , and *14/*14 genotypes classified as poor metabolizer were only present in 4, 2, and 1 subjects, respectively. Mutant genotypes with frequencies of more than 1% were CYP2D6*1/*10 (32.0%), *10/*10 (22.3%), *2/*10 (11.7%), *5/*10 (3.7%), *1/*5 (2.5%), and *10/*41 (1.2%). The relative clearance of metoprolol in CYP2D6*1/*10 , *1/*5 , *10/*10 , *5/*10 , and *5/*5 genotypes were 69%, 57%, 24%, 14% and 9% of CYP2D6*wt/*wt genotype, respectively. These results will be very useful in establishing a strategy for precision medicine related to the genetic polymorphism of CYP2D6 .</abstract><cop>Seoul</cop><pub>Pharmaceutical Society of Korea</pub><pmid>30191460</pmid><doi>10.1007/s12272-018-1075-6</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0253-6269
ispartof Archives of pharmacal research, 2018-09, Vol.41 (9), p.921-930
issn 0253-6269
1976-3786
language eng
recordid cdi_proquest_miscellaneous_2101275530
source MEDLINE; SpringerLink Journals - AutoHoldings
subjects African Continental Ancestry Group - genetics
Asian Continental Ancestry Group - genetics
Cytochrome P-450 CYP2D6 - genetics
Cytochrome P-450 CYP2D6 - metabolism
European Continental Ancestry Group - genetics
Gene Frequency - genetics
Genotype
Humans
Medicine
Pharmacology/Toxicology
Pharmacy
Republic of Korea
Research Article
title CYP2D6 allele frequencies in Korean population, comparison with East Asian, Caucasian and African populations, and the comparison of metabolic activity of CYP2D6 genotypes
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T22%3A09%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=CYP2D6%20allele%20frequencies%20in%20Korean%20population,%20comparison%20with%20East%20Asian,%20Caucasian%20and%20African%20populations,%20and%20the%20comparison%20of%20metabolic%20activity%20of%20CYP2D6%20genotypes&rft.jtitle=Archives%20of%20pharmacal%20research&rft.au=Byeon,%20Ji-Young&rft.date=2018-09-01&rft.volume=41&rft.issue=9&rft.spage=921&rft.epage=930&rft.pages=921-930&rft.issn=0253-6269&rft.eissn=1976-3786&rft_id=info:doi/10.1007/s12272-018-1075-6&rft_dat=%3Cproquest_cross%3E2101275530%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2101275530&rft_id=info:pmid/30191460&rfr_iscdi=true