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Population Genetic Difference of Pharmacogenomic VIP Variants in the Tibetan Population
BACKGROUND: Genetic variation influences drug reaction or adverse prognosis. The purpose of this research was to genotype very important pharmacogenetic (VIP) variants in the Tibetan population. METHODS AND MATERIALS: Blood samples from 200 Tibetans were randomly collected and 59 VIP variants were g...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8379641/ https://www.ncbi.nlm.nih.gov/pubmed/34429635 http://dx.doi.org/10.2147/PGPM.S316711 |
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author | He, Chunjuan Peng, Linna Xing, Shishi Li, Dandan Wang, Li Jin, Tianbo |
author_facet | He, Chunjuan Peng, Linna Xing, Shishi Li, Dandan Wang, Li Jin, Tianbo |
author_sort | He, Chunjuan |
collection | PubMed |
description | BACKGROUND: Genetic variation influences drug reaction or adverse prognosis. The purpose of this research was to genotype very important pharmacogenetic (VIP) variants in the Tibetan population. METHODS AND MATERIALS: Blood samples from 200 Tibetans were randomly collected and 59 VIP variants were genotyped, and then compared our data to 26 other populations in the 1000 project to further analyze and identify significant difference. RESULTS: The results showed that on comparing with most of the 26 populations from the 1000 project, rs4291 (ACE), rs1051296 (SLC19A1) and rs1065852 (CYP2D6) significantly differed in the Tibetan population. Furthermore, three significant loci were related to drug response. In addition, the allele frequency of Tibetans least differed from that of East Asian populations, and most differed from that of Americans. CONCLUSION: Three significant loci of variation ACE rs4291, SLC19A1 rs1051296 and CYP2D6 rs1065852 were associated with drug response. This result will contribute to improving the information of the Tibetan in the pharmacogenomics database, and providing a theoretical basis for clinical individualised drug use in Tibetans. |
format | Online Article Text |
id | pubmed-8379641 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-83796412021-08-23 Population Genetic Difference of Pharmacogenomic VIP Variants in the Tibetan Population He, Chunjuan Peng, Linna Xing, Shishi Li, Dandan Wang, Li Jin, Tianbo Pharmgenomics Pers Med Original Research BACKGROUND: Genetic variation influences drug reaction or adverse prognosis. The purpose of this research was to genotype very important pharmacogenetic (VIP) variants in the Tibetan population. METHODS AND MATERIALS: Blood samples from 200 Tibetans were randomly collected and 59 VIP variants were genotyped, and then compared our data to 26 other populations in the 1000 project to further analyze and identify significant difference. RESULTS: The results showed that on comparing with most of the 26 populations from the 1000 project, rs4291 (ACE), rs1051296 (SLC19A1) and rs1065852 (CYP2D6) significantly differed in the Tibetan population. Furthermore, three significant loci were related to drug response. In addition, the allele frequency of Tibetans least differed from that of East Asian populations, and most differed from that of Americans. CONCLUSION: Three significant loci of variation ACE rs4291, SLC19A1 rs1051296 and CYP2D6 rs1065852 were associated with drug response. This result will contribute to improving the information of the Tibetan in the pharmacogenomics database, and providing a theoretical basis for clinical individualised drug use in Tibetans. Dove 2021-08-16 /pmc/articles/PMC8379641/ /pubmed/34429635 http://dx.doi.org/10.2147/PGPM.S316711 Text en © 2021 He et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research He, Chunjuan Peng, Linna Xing, Shishi Li, Dandan Wang, Li Jin, Tianbo Population Genetic Difference of Pharmacogenomic VIP Variants in the Tibetan Population |
title | Population Genetic Difference of Pharmacogenomic VIP Variants in the Tibetan Population |
title_full | Population Genetic Difference of Pharmacogenomic VIP Variants in the Tibetan Population |
title_fullStr | Population Genetic Difference of Pharmacogenomic VIP Variants in the Tibetan Population |
title_full_unstemmed | Population Genetic Difference of Pharmacogenomic VIP Variants in the Tibetan Population |
title_short | Population Genetic Difference of Pharmacogenomic VIP Variants in the Tibetan Population |
title_sort | population genetic difference of pharmacogenomic vip variants in the tibetan population |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8379641/ https://www.ncbi.nlm.nih.gov/pubmed/34429635 http://dx.doi.org/10.2147/PGPM.S316711 |
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