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  • 期刊

Difference in the Prevalence of CYP2C19 Poor Metabolizers among Racial and Ethnic Groups of Eastern Taiwan

東台灣不同族群間在CYP2C19慢代謝者盛行率上存在差異

摘要


Background: CYP2C19 is an enzyme for drug metabolism, and its genetic polymorphisms produce interpersonal variations in drug responses. The two major loss-of-function alleles for poor metabolizers (PMs) for Asian populations were CYP2C19*2 and CYP2C19*3. This study was conducted to assess whether the prevalence of CYP2C19 PM genotypes differs between Han Chinese and Taiwan Aborigines in Eastern Taiwan.Material and Methods: A total of 955 students were selected from six senior high schools in Hualien County, and 938 (98.2%) of them were genotyped for CYP2C19*2 and CYP2C19*3 by direct sequencing method. Individuals with homozygous CYP2C19*2, homozygous CYP2C19*3 or heterozygous CYP2C19*2/*3 were predicted to have the PM phenotype.Results: The prevalence of CYP2C19*2 and CYP2C19*3 in Taiwan Aborigines were higher than those in Han Chinese (40.1% and 9.1% vs. 30.6% and 5.5%, both p < 0.01). The predicted CYP2C19 PM phenotype in Taiwan Aborigines was also higher (23.3% vs. 13.0%, p < 0.01).Conclusion: We showed there are major differences in the prevalences of CYP2C19 PMs among different ethnic groups in Eastern Taiwan.

並列摘要


Background: CYP2C19 is an enzyme for drug metabolism, and its genetic polymorphisms produce interpersonal variations in drug responses. The two major loss-of-function alleles for poor metabolizers (PMs) for Asian populations were CYP2C19*2 and CYP2C19*3. This study was conducted to assess whether the prevalence of CYP2C19 PM genotypes differs between Han Chinese and Taiwan Aborigines in Eastern Taiwan.Material and Methods: A total of 955 students were selected from six senior high schools in Hualien County, and 938 (98.2%) of them were genotyped for CYP2C19*2 and CYP2C19*3 by direct sequencing method. Individuals with homozygous CYP2C19*2, homozygous CYP2C19*3 or heterozygous CYP2C19*2/*3 were predicted to have the PM phenotype.Results: The prevalence of CYP2C19*2 and CYP2C19*3 in Taiwan Aborigines were higher than those in Han Chinese (40.1% and 9.1% vs. 30.6% and 5.5%, both p < 0.01). The predicted CYP2C19 PM phenotype in Taiwan Aborigines was also higher (23.3% vs. 13.0%, p < 0.01).Conclusion: We showed there are major differences in the prevalences of CYP2C19 PMs among different ethnic groups in Eastern Taiwan.

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