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Genetic polymorphisms of VIP variants in the Tajik ethnic group of northwest China

BACKGROUND: Individual response to medications varies significantly among different populations, and great progress in understanding the molecular basis of drug action has been made in the past 50 years. The field of pharmacogenomics seeks to elucidate inherited differences in drug disposition and e...

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Autores principales: Zhang, Jiayi, Jin, Tianbo, Yunus, Zulfiya, Li, Xiaolan, Geng, Tingting, Wang, Hong, Cui, Yali, Chen, Chao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189671/
https://www.ncbi.nlm.nih.gov/pubmed/25266489
http://dx.doi.org/10.1186/s12863-014-0102-y
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author Zhang, Jiayi
Jin, Tianbo
Yunus, Zulfiya
Li, Xiaolan
Geng, Tingting
Wang, Hong
Cui, Yali
Chen, Chao
author_facet Zhang, Jiayi
Jin, Tianbo
Yunus, Zulfiya
Li, Xiaolan
Geng, Tingting
Wang, Hong
Cui, Yali
Chen, Chao
author_sort Zhang, Jiayi
collection PubMed
description BACKGROUND: Individual response to medications varies significantly among different populations, and great progress in understanding the molecular basis of drug action has been made in the past 50 years. The field of pharmacogenomics seeks to elucidate inherited differences in drug disposition and effects. While we know that different populations and ethnic groups are genetically heterogeneous, we have not found any pharmacogenomics information regarding minority groups, such as the Tajik ethnic group in northwest China. RESULTS: We genotyped 85 Very Important Pharmacogene (VIP) variants selected from PharmGKB in 100 unrelated, healthy Tajiks from the Xinjiang Uygur Autonomous Region and compared our data with HapMap data from four major populations around the world: Han Chinese (CHB), Japanese in Tokyo (JPT), Utah Residents with Northern and Western European Ancestry (CEU), and Yorubia in Ibadan, Nigeria (YRI). We found that Tajiks differed from CHB, JPT and YRI in 30, 32, and 32 of the selected VIP genotypes respectively (p < 0.005), while differences between Tajiks and CEU were found in only 6 of the genotypes (p < 0.005). Haplotype analysis also demonstrated differences between the Tajiks and the other four populations. CONCLUSION: Our results contribute to the pharmacogenomics database of the Tajik ethnic group and provide a theoretical basis for safer drug administration that may be useful for diagnosing and treating disease in this population. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12863-014-0102-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-41896712014-10-09 Genetic polymorphisms of VIP variants in the Tajik ethnic group of northwest China Zhang, Jiayi Jin, Tianbo Yunus, Zulfiya Li, Xiaolan Geng, Tingting Wang, Hong Cui, Yali Chen, Chao BMC Genet Research Article BACKGROUND: Individual response to medications varies significantly among different populations, and great progress in understanding the molecular basis of drug action has been made in the past 50 years. The field of pharmacogenomics seeks to elucidate inherited differences in drug disposition and effects. While we know that different populations and ethnic groups are genetically heterogeneous, we have not found any pharmacogenomics information regarding minority groups, such as the Tajik ethnic group in northwest China. RESULTS: We genotyped 85 Very Important Pharmacogene (VIP) variants selected from PharmGKB in 100 unrelated, healthy Tajiks from the Xinjiang Uygur Autonomous Region and compared our data with HapMap data from four major populations around the world: Han Chinese (CHB), Japanese in Tokyo (JPT), Utah Residents with Northern and Western European Ancestry (CEU), and Yorubia in Ibadan, Nigeria (YRI). We found that Tajiks differed from CHB, JPT and YRI in 30, 32, and 32 of the selected VIP genotypes respectively (p < 0.005), while differences between Tajiks and CEU were found in only 6 of the genotypes (p < 0.005). Haplotype analysis also demonstrated differences between the Tajiks and the other four populations. CONCLUSION: Our results contribute to the pharmacogenomics database of the Tajik ethnic group and provide a theoretical basis for safer drug administration that may be useful for diagnosing and treating disease in this population. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12863-014-0102-y) contains supplementary material, which is available to authorized users. BioMed Central 2014-09-30 /pmc/articles/PMC4189671/ /pubmed/25266489 http://dx.doi.org/10.1186/s12863-014-0102-y Text en © Zhang et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Zhang, Jiayi
Jin, Tianbo
Yunus, Zulfiya
Li, Xiaolan
Geng, Tingting
Wang, Hong
Cui, Yali
Chen, Chao
Genetic polymorphisms of VIP variants in the Tajik ethnic group of northwest China
title Genetic polymorphisms of VIP variants in the Tajik ethnic group of northwest China
title_full Genetic polymorphisms of VIP variants in the Tajik ethnic group of northwest China
title_fullStr Genetic polymorphisms of VIP variants in the Tajik ethnic group of northwest China
title_full_unstemmed Genetic polymorphisms of VIP variants in the Tajik ethnic group of northwest China
title_short Genetic polymorphisms of VIP variants in the Tajik ethnic group of northwest China
title_sort genetic polymorphisms of vip variants in the tajik ethnic group of northwest china
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189671/
https://www.ncbi.nlm.nih.gov/pubmed/25266489
http://dx.doi.org/10.1186/s12863-014-0102-y
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