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Genetic Diversity of HLA Class I and Class II Alleles in Thai Populations: Contribution to Genotype-Guided Therapeutics
Human leukocyte antigen (HLA) class I and II are known to have association with severe cutaneous adverse reactions (SCARs) when exposing to certain drug treatment. Due to genetic differences at population level, drug hypersensitivity reactions are varied, and thus common pharmacogenetics markers for...
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Published in: | Frontiers in pharmacology 2020-02, Vol.11, p.78-78 |
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creator | Satapornpong, Patompong Jinda, Pimonpan Jantararoungtong, Thawinee Koomdee, Napatrupron Chaichan, Chonlawat Pratoomwun, Jirawat Na Nakorn, Chalitpon Aekplakorn, Wichai Wilantho, Alisa Ngamphiw, Chumpol Tongsima, Sissades Sukasem, Chonlaphat |
description | Human leukocyte antigen (HLA) class I and II are known to have association with severe cutaneous adverse reactions (SCARs) when exposing to certain drug treatment. Due to genetic differences at population level, drug hypersensitivity reactions are varied, and thus common pharmacogenetics markers for one country might be different from another country, for instance,
is associated with carbamazepine (CBZ)-induced SCARs in European and Japanese while
is associated with CBZ-induced Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) among Taiwanese and Southeast Asian. Such differences pose a major challenge to prevent drug hypersensitivity when pharmacogenetics cannot be ubiquitously and efficiently translated into clinic. Therefore, a population-wide study of the distribution of HLA-pharmacogenetics markers is needed. This work presents a study of Thai
alleles on both
class I and II genes from 470 unrelated Thai individuals by means of polymerase chain reaction sequence-specific oligonucleotide (PCR-SSO) in which oligonucleotide probes along the stretches of
genes were genotyped. These 470 individuals were selected according to their regional locations, which were from North, Northeast, South, Central, and a capital city, Bangkok. Top ranked
alleles in Thai population include
(26.06%),
(14.04%),
(17.13%),
(15.32%),
(24.89%), and
(21.28%). The results revealed that the distribution of HLA-pharmacogenetics alleles from the South had more HLA-B75 family that a typical
pharmacogenetics test for SJS/TEN screening would not cover. Besides the view across the nation, when compared
alleles from Thai population with
alleles from both European and Asian countries, the distribution landscape of
-associated drug hypersensitivity across many countries could be observed. Consequently, this pharmacogenetics database offers a comprehensive view of pharmacogenetics marker distribution in Thailand that could be used as a reference for other Southeast Asian countries to validate the feasibility of their future pharmacogenetics deployment. |
doi_str_mv | 10.3389/fphar.2020.00078 |
format | article |
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is associated with carbamazepine (CBZ)-induced SCARs in European and Japanese while
is associated with CBZ-induced Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) among Taiwanese and Southeast Asian. Such differences pose a major challenge to prevent drug hypersensitivity when pharmacogenetics cannot be ubiquitously and efficiently translated into clinic. Therefore, a population-wide study of the distribution of HLA-pharmacogenetics markers is needed. This work presents a study of Thai
alleles on both
class I and II genes from 470 unrelated Thai individuals by means of polymerase chain reaction sequence-specific oligonucleotide (PCR-SSO) in which oligonucleotide probes along the stretches of
genes were genotyped. These 470 individuals were selected according to their regional locations, which were from North, Northeast, South, Central, and a capital city, Bangkok. Top ranked
alleles in Thai population include
(26.06%),
(14.04%),
(17.13%),
(15.32%),
(24.89%), and
(21.28%). The results revealed that the distribution of HLA-pharmacogenetics alleles from the South had more HLA-B75 family that a typical
pharmacogenetics test for SJS/TEN screening would not cover. Besides the view across the nation, when compared
alleles from Thai population with
alleles from both European and Asian countries, the distribution landscape of
-associated drug hypersensitivity across many countries could be observed. Consequently, this pharmacogenetics database offers a comprehensive view of pharmacogenetics marker distribution in Thailand that could be used as a reference for other Southeast Asian countries to validate the feasibility of their future pharmacogenetics deployment.</description><identifier>ISSN: 1663-9812</identifier><identifier>EISSN: 1663-9812</identifier><identifier>DOI: 10.3389/fphar.2020.00078</identifier><identifier>PMID: 32180714</identifier><language>eng</language><publisher>Switzerland: Frontiers Media S.A</publisher><subject>HLA class I ; HLA class II ; human leukocyte antigen ; pharmacogenetic marker ; Pharmacology ; Thai population</subject><ispartof>Frontiers in pharmacology, 2020-02, Vol.11, p.78-78</ispartof><rights>Copyright © 2020 Satapornpong, Jinda, Jantararoungtong, Koomdee, Chaichan, Pratoomwun, Na Nakorn, Aekplakorn, Wilantho, Ngamphiw, Tongsima and Sukasem.</rights><rights>Copyright © 2020 Satapornpong, Jinda, Jantararoungtong, Koomdee, Chaichan, Pratoomwun, Na Nakorn, Aekplakorn, Wilantho, Ngamphiw, Tongsima and Sukasem 2020 Satapornpong, Jinda, Jantararoungtong, Koomdee, Chaichan, Pratoomwun, Na Nakorn, Aekplakorn, Wilantho, Ngamphiw, Tongsima and Sukasem</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c528t-8c85da30d218618241af327683b16af08acbaa83d1c14903084a77ae571fd0743</citedby><cites>FETCH-LOGICAL-c528t-8c85da30d218618241af327683b16af08acbaa83d1c14903084a77ae571fd0743</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057685/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057685/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32180714$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Satapornpong, Patompong</creatorcontrib><creatorcontrib>Jinda, Pimonpan</creatorcontrib><creatorcontrib>Jantararoungtong, Thawinee</creatorcontrib><creatorcontrib>Koomdee, Napatrupron</creatorcontrib><creatorcontrib>Chaichan, Chonlawat</creatorcontrib><creatorcontrib>Pratoomwun, Jirawat</creatorcontrib><creatorcontrib>Na Nakorn, Chalitpon</creatorcontrib><creatorcontrib>Aekplakorn, Wichai</creatorcontrib><creatorcontrib>Wilantho, Alisa</creatorcontrib><creatorcontrib>Ngamphiw, Chumpol</creatorcontrib><creatorcontrib>Tongsima, Sissades</creatorcontrib><creatorcontrib>Sukasem, Chonlaphat</creatorcontrib><title>Genetic Diversity of HLA Class I and Class II Alleles in Thai Populations: Contribution to Genotype-Guided Therapeutics</title><title>Frontiers in pharmacology</title><addtitle>Front Pharmacol</addtitle><description>Human leukocyte antigen (HLA) class I and II are known to have association with severe cutaneous adverse reactions (SCARs) when exposing to certain drug treatment. Due to genetic differences at population level, drug hypersensitivity reactions are varied, and thus common pharmacogenetics markers for one country might be different from another country, for instance,
is associated with carbamazepine (CBZ)-induced SCARs in European and Japanese while
is associated with CBZ-induced Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) among Taiwanese and Southeast Asian. Such differences pose a major challenge to prevent drug hypersensitivity when pharmacogenetics cannot be ubiquitously and efficiently translated into clinic. Therefore, a population-wide study of the distribution of HLA-pharmacogenetics markers is needed. This work presents a study of Thai
alleles on both
class I and II genes from 470 unrelated Thai individuals by means of polymerase chain reaction sequence-specific oligonucleotide (PCR-SSO) in which oligonucleotide probes along the stretches of
genes were genotyped. These 470 individuals were selected according to their regional locations, which were from North, Northeast, South, Central, and a capital city, Bangkok. Top ranked
alleles in Thai population include
(26.06%),
(14.04%),
(17.13%),
(15.32%),
(24.89%), and
(21.28%). The results revealed that the distribution of HLA-pharmacogenetics alleles from the South had more HLA-B75 family that a typical
pharmacogenetics test for SJS/TEN screening would not cover. Besides the view across the nation, when compared
alleles from Thai population with
alleles from both European and Asian countries, the distribution landscape of
-associated drug hypersensitivity across many countries could be observed. Consequently, this pharmacogenetics database offers a comprehensive view of pharmacogenetics marker distribution in Thailand that could be used as a reference for other Southeast Asian countries to validate the feasibility of their future pharmacogenetics deployment.</description><subject>HLA class I</subject><subject>HLA class II</subject><subject>human leukocyte antigen</subject><subject>pharmacogenetic marker</subject><subject>Pharmacology</subject><subject>Thai population</subject><issn>1663-9812</issn><issn>1663-9812</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkc1vEzEQxVcIRKvSOyfkI5cN_ti1vRyQogBppEhwKGdr1h-NK2e92LtF-e9xkrZqTx573vzmWa-qPhK8YEx2X9y4g7SgmOIFxljIN9Ul4ZzVnST07Yv6orrO-b5IMOs6xpv31QWjRGJBmsvq39oOdvIaffcPNmU_HVB06Ga7RKsAOaMNgsE81Ru0DMEGm5Ef0O0OPPodxznA5OOQv6JVHKbk-_l4RVNEBR2nw2jr9eyNNWXCJhht6ev8oXrnIGR7_XheVX9-_rhd3dTbX-vNarmtdUvlVEstWwMMm2KYE0kbAo5RwSXrCQeHJegeQDJDNGk6zLBsQAiwrSDOYNGwq2pz5poI92pMfg_poCJ4dXqI6U5BKoaCVaJwNOW2MaJvKNO9cE5zaahoeDHjCuvbmTXO_d4abct3IbyCvu4Mfqfu4oMSuC2W2wL4_AhI8e9s86T2PmsbAgw2zllRJiTGpJOySPFZqlPMOVn3vIZgdYxfneJXx_jVKf4y8umlveeBp7DZf0s1rFk</recordid><startdate>20200227</startdate><enddate>20200227</enddate><creator>Satapornpong, Patompong</creator><creator>Jinda, Pimonpan</creator><creator>Jantararoungtong, Thawinee</creator><creator>Koomdee, Napatrupron</creator><creator>Chaichan, Chonlawat</creator><creator>Pratoomwun, Jirawat</creator><creator>Na Nakorn, Chalitpon</creator><creator>Aekplakorn, Wichai</creator><creator>Wilantho, Alisa</creator><creator>Ngamphiw, Chumpol</creator><creator>Tongsima, Sissades</creator><creator>Sukasem, Chonlaphat</creator><general>Frontiers Media S.A</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20200227</creationdate><title>Genetic Diversity of HLA Class I and Class II Alleles in Thai Populations: Contribution to Genotype-Guided Therapeutics</title><author>Satapornpong, Patompong ; Jinda, Pimonpan ; Jantararoungtong, Thawinee ; Koomdee, Napatrupron ; Chaichan, Chonlawat ; Pratoomwun, Jirawat ; Na Nakorn, Chalitpon ; Aekplakorn, Wichai ; Wilantho, Alisa ; Ngamphiw, Chumpol ; Tongsima, Sissades ; Sukasem, Chonlaphat</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c528t-8c85da30d218618241af327683b16af08acbaa83d1c14903084a77ae571fd0743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>HLA class I</topic><topic>HLA class II</topic><topic>human leukocyte antigen</topic><topic>pharmacogenetic marker</topic><topic>Pharmacology</topic><topic>Thai population</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Satapornpong, Patompong</creatorcontrib><creatorcontrib>Jinda, Pimonpan</creatorcontrib><creatorcontrib>Jantararoungtong, Thawinee</creatorcontrib><creatorcontrib>Koomdee, Napatrupron</creatorcontrib><creatorcontrib>Chaichan, Chonlawat</creatorcontrib><creatorcontrib>Pratoomwun, Jirawat</creatorcontrib><creatorcontrib>Na Nakorn, Chalitpon</creatorcontrib><creatorcontrib>Aekplakorn, Wichai</creatorcontrib><creatorcontrib>Wilantho, Alisa</creatorcontrib><creatorcontrib>Ngamphiw, Chumpol</creatorcontrib><creatorcontrib>Tongsima, Sissades</creatorcontrib><creatorcontrib>Sukasem, Chonlaphat</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Frontiers in pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Satapornpong, Patompong</au><au>Jinda, Pimonpan</au><au>Jantararoungtong, Thawinee</au><au>Koomdee, Napatrupron</au><au>Chaichan, Chonlawat</au><au>Pratoomwun, Jirawat</au><au>Na Nakorn, Chalitpon</au><au>Aekplakorn, Wichai</au><au>Wilantho, Alisa</au><au>Ngamphiw, Chumpol</au><au>Tongsima, Sissades</au><au>Sukasem, Chonlaphat</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic Diversity of HLA Class I and Class II Alleles in Thai Populations: Contribution to Genotype-Guided Therapeutics</atitle><jtitle>Frontiers in pharmacology</jtitle><addtitle>Front Pharmacol</addtitle><date>2020-02-27</date><risdate>2020</risdate><volume>11</volume><spage>78</spage><epage>78</epage><pages>78-78</pages><issn>1663-9812</issn><eissn>1663-9812</eissn><abstract>Human leukocyte antigen (HLA) class I and II are known to have association with severe cutaneous adverse reactions (SCARs) when exposing to certain drug treatment. Due to genetic differences at population level, drug hypersensitivity reactions are varied, and thus common pharmacogenetics markers for one country might be different from another country, for instance,
is associated with carbamazepine (CBZ)-induced SCARs in European and Japanese while
is associated with CBZ-induced Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) among Taiwanese and Southeast Asian. Such differences pose a major challenge to prevent drug hypersensitivity when pharmacogenetics cannot be ubiquitously and efficiently translated into clinic. Therefore, a population-wide study of the distribution of HLA-pharmacogenetics markers is needed. This work presents a study of Thai
alleles on both
class I and II genes from 470 unrelated Thai individuals by means of polymerase chain reaction sequence-specific oligonucleotide (PCR-SSO) in which oligonucleotide probes along the stretches of
genes were genotyped. These 470 individuals were selected according to their regional locations, which were from North, Northeast, South, Central, and a capital city, Bangkok. Top ranked
alleles in Thai population include
(26.06%),
(14.04%),
(17.13%),
(15.32%),
(24.89%), and
(21.28%). The results revealed that the distribution of HLA-pharmacogenetics alleles from the South had more HLA-B75 family that a typical
pharmacogenetics test for SJS/TEN screening would not cover. Besides the view across the nation, when compared
alleles from Thai population with
alleles from both European and Asian countries, the distribution landscape of
-associated drug hypersensitivity across many countries could be observed. Consequently, this pharmacogenetics database offers a comprehensive view of pharmacogenetics marker distribution in Thailand that could be used as a reference for other Southeast Asian countries to validate the feasibility of their future pharmacogenetics deployment.</abstract><cop>Switzerland</cop><pub>Frontiers Media S.A</pub><pmid>32180714</pmid><doi>10.3389/fphar.2020.00078</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | HLA class I HLA class II human leukocyte antigen pharmacogenetic marker Pharmacology Thai population |
title | Genetic Diversity of HLA Class I and Class II Alleles in Thai Populations: Contribution to Genotype-Guided Therapeutics |
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