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...
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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> |
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ispartof | Archives of pharmacal research, 2018-09, Vol.41 (9), p.921-930 |
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language | eng |
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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 |
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