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N-乙酰基转移酶-2(NAT2)基因多态性与塞尔维亚人群中的酶活性:白人族群中快速乙酰化酶的前所未有的高发生率。

N-Acetyltransferase-2 (NAT2) gene polymorphisms and enzyme activity in Serbs: unprecedented high prevalence of rapid acetylators in a White population.

机构信息

Division of Clinical Pharmacology, Department of Laboratory Medicine, Karolinska Institutet, Karolinska University Hospital, Huddinge, Stockholm, Sweden.

出版信息

J Clin Pharmacol. 2011 Jul;51(7):994-1003. doi: 10.1177/0091270010377630. Epub 2010 Aug 27.

DOI:10.1177/0091270010377630
PMID:20801937
Abstract

The aim of this study was to investigate N-acetyltransferase 2 (NAT2) genetic polymorphism and enzyme activity in Serbs, and to examine the influence of NAT2 genotype, sex, and smoking on the phenotype. Genotyping for 190C>T, 282C>T, 341T>C, 403C>G, 411T>A, 481C>T, 590G>A, 803A>G, and 857G>A in the NAT2 gene, was performed in 140 healthy Serbs. NAT2 activity was determined as AFMU/ (AFMU + 1X + 1U) urinary ratio in 100 subjects using caffeine as a probe. The most frequent NAT2 haplotypes were NAT25B (38.2%), NAT26A (26.0%), and NAT24 (24.4%). The log-transformed NAT2 activity indices exhibited trimodal distribution with 9%, 36%, and 55% of slow, intermediate, and rapid acetylators, respectively. Significant NAT2 genotype-phenotype correlation was observed (P < .0001). The frequency of NAT110 and NAT111 were 27.5% and 6.9%, respectively. There was no significant influence of sex or cigarette smoking on NAT2 enzyme activity. Eight subjects displayed rapid NAT2 acetylators phenotype despite being homozygous for NAT2 slow alleles, and NAT1 fast acetylators genotype (NAT110 and NAT1*11) had no implication. In contrast to other white populations described hitherto, rapid acetylator is the predominant NAT2 phenotype in Serbs. NAT2 genotype, but not sex and cigarette smoking, influence enzyme activity. NAT1 fast acetylators genotypes do not contribute for NAT2 genotype-phenotype discordance.

摘要

本研究旨在探讨塞尔维亚人群中 N-乙酰基转移酶 2(NAT2)基因多态性和酶活性,并研究 NAT2 基因型、性别和吸烟对表型的影响。对 140 名健康塞尔维亚人进行了 NAT2 基因 190C>T、282C>T、341T>C、403C>G、411T>A、481C>T、590G>A、803A>G 和 857G>A 的基因分型。在 100 名受试者中,使用咖啡因作为探针,通过 AFMU/(AFMU+1X+1U)尿比值确定 NAT2 活性。最常见的 NAT2 单倍型为 NAT25B(38.2%)、NAT26A(26.0%)和 NAT24(24.4%)。经对数转换的 NAT2 活性指数呈三峰分布,分别为 9%、36%和 55%的慢乙酰化、中速乙酰化和快速乙酰化。观察到 NAT2 基因型-表型相关性显著(P<.0001)。NAT110 和 NAT111 的频率分别为 27.5%和 6.9%。性别或吸烟对 NAT2 酶活性无显著影响。尽管 8 名受试者均为 NAT2 慢等位基因纯合子,但表现为快速 NAT2 乙酰化表型,且 NAT1 快速乙酰化基因型(NAT110 和 NAT1*11)无影响。与迄今为止描述的其他白人人群不同,快速乙酰化是塞尔维亚人群中主要的 NAT2 表型。NAT2 基因型而非性别和吸烟会影响酶活性。NAT1 快速乙酰化基因型不会导致 NAT2 基因型-表型不一致。

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