The influence of NAT2 genotypes on the plasma concentration of isoniazid and acetylisoniazid in Chinese pulmonary tuberculosis patients

被引:24
作者
Chen, B
Li, JH
Xu, YM
Wang, J
Cao, XM
机构
[1] Jinling Hosp, Dept Clin Pharmacol, Nanjing 210002, Peoples R China
[2] Nanjing Chest Hosp, Dept Pharm, Nanjing 210029, Peoples R China
基金
中国国家自然科学基金;
关键词
isomazid (INH); acetylisoniazid (AcINH); N-acetyltransferase 2 (NAT2); genotype; tuberculosis;
D O I
10.1016/j.cca.2005.08.012
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Isoniazid (INH) is widely used in the therapy of tuberculosis. Poor metabolizer (PM) of the NAT2 is an important reason of inter-individual difference of the plasma INH concentration. We studied the relationship between NAT2 genotype and INH and its metabolite acetylisoniazid (AcINH) concentration in Chinese people. Method: Forty-six tuberculosis patients were enrolled in the study. Each patient took 300 mg INH daily for at least 7 days. Two hours after the INH was given, the vein blood was drawn. NAT2 genotypes of patients were detected by a reverse dot blot (RDB) method. The plasma concentration of INH and AcINH was determined by a precolumn derivization HPLC method. Results: In 46 patients, homozygous mutant (m/m), heterozygous mutant (m/wt) and homozygous wild-type (wt/wt) subjects were 7, 22 and 17, respectively. Plasma concentration of INH and AcINH were 12.74 +/- 10.51 and 12.49 +/- 9.61 mu mol/l, respectively. There was no statistical difference among 3 genotypes. The ratios of AcINH and INH (R-A/I) of 3 genotypes were 0.67 +/- 0.34, 0.88 +/- 0.40 and 1.69 +/- 0.66, respectively. The RAM of m/m and m/wt group were significantly lower than wt/wt group (P < 0.01). Conclusion: The results suggest that various NAT2 genotypes in Chinese tuberculosis patients have great impact on the metabolism capacity of NAT2. This finding maybe valuable in the rational use of relevant drugs. (c) 2005 Elsevier B.V All rights reserved.
引用
收藏
页码:104 / 108
页数:5
相关论文
共 31 条
  • [1] Ahn C, 2003, PERITON DIALYSIS INT, V23, P362
  • [2] GENOTYPE-PHENOTYPE DISCORDANCE FOR HUMAN ARYLAMINE N-ACETYLTRANSFERASE (NAT2) REVEALS A NEW SLOW-ACETYLATOR ALLELE COMMON IN AFRICAN-AMERICANS
    BELL, DA
    TAYLOR, JA
    BUTLER, MA
    STEPHENS, EA
    WIEST, J
    BRUBAKER, LH
    KADLUBAR, FF
    LUCIER, GW
    [J]. CARCINOGENESIS, 1993, 14 (08) : 1689 - 1692
  • [3] CASCORBI I, 1995, AM J HUM GENET, V57, P591
  • [4] [陈冰 Chen Bing], 2004, [中国药理学通报, Chinese Pharmacological Bulletin], V20, P1269
  • [5] Serum osteocalcin in relation to calcaneal bone mineral density in elderly men and women:: a 5-year follow-up
    Cheng, SL
    Suominen, H
    Väänänen, K
    Käkönen, SM
    Pettersson, K
    Heikkinen, E
    [J]. JOURNAL OF BONE AND MINERAL METABOLISM, 2002, 20 (01) : 49 - 56
  • [6] Effects of gender, AIDS, and acetylator status on intrapulmonary concentrations of isoniazid
    Conte, JE
    Golden, JA
    McQuitty, M
    Kipps, J
    Duncan, S
    McKenna, E
    Zurlinden, E
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (08) : 2358 - 2364
  • [7] DEGUCHI T, 1990, J BIOL CHEM, V265, P12757
  • [8] GENETICALLY-DETERMINED DIFFERENCES IN DRUG-METABOLISM AS A RISK FACTOR IN DRUG TOXICITY
    EICHELBAUM, M
    KROEMER, HK
    MIKUS, G
    [J]. TOXICOLOGY LETTERS, 1992, 64-5 : 115 - 122
  • [9] ELLARD GA, 1976, CLIN PHARMACOL THER, V19, P610
  • [10] CEREBROSPINAL-FLUID DRUG CONCENTRATIONS AND THE TREATMENT OF TUBERCULOUS MENINGITIS
    ELLARD, GA
    HUMPHRIES, MJ
    ALLEN, BW
    [J]. AMERICAN REVIEW OF RESPIRATORY DISEASE, 1993, 148 (03): : 650 - 655