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The Diversity of CYP2C19 Polymorphisms in the Thai Population: Implications for Precision Medicine
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Metadata
Document Title
The Diversity of CYP2C19 Polymorphisms in the Thai Population: Implications for Precision Medicine
Author
Nakhonsri V., John S., Panumasmontol H., Jantorn M., Chanthot P., Hanpramukkun N., Meelarp S., Sukasem C., Tongsima S., Hasatsri S., Prawang A., Thaingtamtanha T., Vanwong N., Atasilp C., Chamnanphon M., Jinda P., Satapornpong P.
Affiliations
National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Pathum Thani, Thailand; Division of Pharmacogenomics and Personalized Medicine, Department of Pathology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand; Laboratory for Pharmacogenomics, Somdech Phra Debaratana Medical Center (SDMC), Ramathibodi Hospital, Bangkok, Thailand; Division of General Pharmacy Practice, Department of Pharmaceutical Care, College of Pharmacy, Rangsit University, Pathum Thani, Thailand; Excellence Pharmacogenomics and Precision Medicine Centre, College of Pharmacy, Rangsit University, Pathum Thani, Thailand; Division of Pharmaceutical Technology, Department of Industrial Pharmacy, College of Pharmacy, Rangsit University, Pathum Thani, Thailand; Ounjai Medical Clinic, Bangsue, Bangkok, Thailand; Division of Pharmacy Practice, Department of Pharmaceutical Care, College of Pharmacy, Rangsit University, Pathum Thani, Thailand; Department of Chemistry and Biology, University of Siegen, Siegen, Germany; Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, ON, Canada; Department of Clinical Chemistry, Faculty of Allied Health Sciences, Chulalongkorn University, Bangkok, Thailand; Department of Clinical Chemistry, SYstems Neuroscience of Autism & PSychiatric Disorders (SYNAPS) Research Unit, Faculty of Allied Health Sciences, Chulalongkorn University, Bangkok, Thailand; Chulabhorn International College of Medicine, Thammasat University, Pathumthani, Thailand; Department of Pathology, Faculty of Medicine, Srinakharinwirot University, Nakornnayok, Thailand
Source Title
Application of Clinical Genetics
ISSN
1178704X
Year
2024
Volume
17
Page
95
Open Access
All Open Access, Gold
Publisher
Dove Medical Press Ltd
DOI
10.2147/TACG.S463965
Abstract
Introduction: CYP2C19 plays a major role in the metabolism of various drugs. The most common genetic variants were the CYP2C19*2 and *3 alleles (rs4244285 and rs4986893, non-functional variants). In previous studies, we found that genetic poly-morphisms in CYP2C19 variants influenced the active metabolites of clopidogrel and caused major adverse cardiovascular and cerebrovascular effects. However, the distribution of CYP2C19 varies among ethnic groups and according to adverse drug reactions. This study aimed to investigate the frequency of CYP2C19 genetic polymorphisms in the Thai population and analyze the differences in the frequency of CYP2C19 genetic polymorphisms between Thai and other populations. Methods: This study enrolled 211 unrelated healthy Thai individuals in total. We performed a real-time polymerase chain reaction to genotype CYP2C19*2 (681G > A) and CYP2C19*3 (636G > A). Results: In the Thai population, the CYP2C19*1 allele was the most prevalent at 70.14%, while the CYP2C19*2 and *3 alleles were found at frequencies of 25.36% and 4.50%, respectively. Conversely, the CYP2C19*3 allele was not detected in Caucasian, Hispanic, African, Italian, Macedonian, Tanzanian, or North Indian populations. The phenotypic profile of this gene revealed that the frequency of intermediate metabolizers (IMs) is nearly equal to that of extensive metabolizers (EMs), at 42.65% and 48.82% respectively, with genotypes *1/*2 (36.02%) and *1/*3 (6.63%). Likewise, poor metabolizers (PMs) with genotypes *2/*2 (6.16%), *2/*3 (2.37%), and *3/*3 (<1%) are more prevalent in our population as well. Conclusion: The distribution of CYP2C19 genotype and phenotype influenced by non-functional alleles has potential as a pharmacogenomics biomarker for precision medicine and is dependent on an ethnic-specific genetic variation database. © 2024 Nakhonsri et al.
License
CC BY-NC
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Authors
Publication Source
Scopus