Comparative analysis of N-acetylation polymorphism in humans as determined by phenotyping and genotyping

• Published in: Russian journal of genetics Vol. 42; no. 8; pp. 947 - 953
• Main Authors: Goldenkova-Pavlova, I. V., Brouskin, S. A., Abdeev, R. M., Markarova, E. V., Bigvava, S. G., Radkevich, L. A., Kurdanov, H. A., Kozhekbaeva, Zh. M., Glotov, A. S., Gra, O. A., Zasedatelev, A. S., Nasedkina, T. V., Piruzyan, E. S.
• Format: Journal Article
• Language: English
• Published: 01.08.2006
• ISSN: 1022-7954; 1608-3369
• DOI: 10.1134/S1022795406080151

The N-acetylation polymorphisms of volunteers from the Moscow population analyzed by phenotyping and genotyping have been compared. The ratios between the proportions of fast acetylators (FAs) and slow acetylators (SAs) estimated by phenotyping and genotyping do not differ significantly from each other (47 and 44%, respectively). The absolute acetylation rate widely varies in both FAs and SAs. The NAT2 genotype and allele frequencies in the population sample have been calculated. The most frequent alleles are NAT2*4 (a 'fast' allele), NAT2*5, and NAT2*6 ('slow' alleles); the most frequent genotypes are NAT2*5/*5, NAT2*4/*6, and NAT2*4/*5. Comparative analysis of N-acetylation polymorphism estimated by phenotyping and genotyping in the same subjects has shown a complete concordance between the phenotype and genotype in only 62 out of 75 subjects (87%). Comparative characteristics and presumed applications of the two approaches (quantitative estimation of acetylation rate and qualitative determination of the acetylator genotype) to the identification of individual acetylation status are presented.