Phenotypic and genotypic analysis of the TPMT in Han nationality in Beijing
ZHANG Bo1, XU Xiao-wei1,ZENG Xue-jun2, LI Da-kui1
Author information+
1. Department of Pharmacy, Peking,Union Medicine College Hospital,Peking Union Medical College-Chinese Academy of Medical Sciences, Beijing 100730, China;2.Department of Rheumatology and Immunology, Peking Union Medicine College Hospital Peking Union Medical College-Chinese Academy of Medical Sciences,Beijing 100730,China
OBJECTIVE To gain an insight into the genetic polymorphism of thiopurine methyltransferase (TPMT) in Han nationality in Beijing in China. METHODS The erythrocyte TPMT activity in 269 healthy Chinese volunteers and 95 patients with autoimmune disease were investigated by HPLC. The genotype assay was based on special sequence primer-polymerase chain reaction (SSP-PCR) and polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) .RESULTS The TPMT activity of 269 healthy volunteers was normally distributed, ranged from 7.23 to 21.40 μmol·h-1·L-1 RBCs, x±s was (13.27±2.19)μmol·h-1·L-1 RBCs. The possible cut-off point for high TPMT activity and low activity subject was 10.48μmol·h-1·L-1 RBCs. There were 17 subjects with low activity (6.3%) and 252 subjects with high activity (93.7%) , and no TPMT deficiency subject was found. The TPMT activity in male subjects was higher than that in female subjects, (13.43±2.27)μmol·h-1·L-1 RBCs vs(12.92±1.97)μmol·h-1·L-1 RBCs, respectively. The TPMT activity of patients ranged from 3.50 to 40.12μmol·h-1·L-1 RBCs, x±s was (15.72±4.99)μmol·h-1·L-1 RBCs, which was higher than that of healthy volunteers, but the difference was not significant. 14 subjects with high TPMT activity had no mutant alleles, while 5 of 10 subjects with low activity had mutant alleles: one of them had TPMT * 2 mutant allele, 5 of them had TPMT * 3C mutant allele. CONCLUSION The TPMT activity of Han nationality was normally distributed,male had higher activity than female; Patients had higher activity than healthy volunteers, but the difference was not significant; the interindividual variation of patients was larger than that of healthy volunteers.
ZHNG o;XU Xio-wei;ZENG Xue-jun;LI D-kui.
Phenotypic and genotypic analysis of the TPMT in Han nationality in Beijing [J]. Chinese Pharmaceutical Journal, 2005, 39(22): 1730-1733
{{custom_sec.title}}
{{custom_sec.title}}
{{custom_sec.content}}
参考文献
[1]Collie-Duguid ESR, Pritchard SC, Powrie RH,et al.The frequency and distribution of thiopurine methyltransferase alleles in Caucasian and Asian populations [J].Pharmacogenetics,1999,9:37.
[2]粱爱斌,顾龙君,叶裕春.上海地区汉族人巯嘌呤甲基转移酶活性及相关基因型分析[J].中华血液学杂志,2000,21(4):211.
[3]Leipold G, Schutz E, Haas JP,et al.Azathiopurine-induced severe pancytopenia due to a homozygous two-point mutation of the thiopurine methyltransferase gene in a patient with juvenile HLA-B27-associated spondylarthritis[J].Arthritis Rheum,1997,40(10): 1896.
[4]张波,徐小薇,付强,等.人红细胞中巯嘌呤甲基转移酶活性的HPLC测定法[J].中国药学杂志,2004,39(12):941.
[5]Weinshilboum RM, Sladek SL. Mercaptopurine pharmacogenetics: monogenic inheritance of erythrocyte thiopurine methyltransferase activity [J]. Am J Hum Genet,1980,32: 651.
[6]Klemetsdal B, Tollefsen E, Leoennechen T,et al.Interethenic difference in thiopurine methyltransferase activity[J].Clin Pharmacol Ther,1992,51(1): 24.
[7]Jones CD, Smart C, Titus A,et al. Thiopurine methyltransferase activity in a sample population of black subjects in Klorida[J].Clin Pharmacol Ther,1993,53(3): 348.
[8]Mcleod HL, Lin JS, Scott EP,et al. Thiopurine methyltransferase activity in American white subjects and black subjects [J].Clin Pharmacol Ther,1994, 55(1):15.
[9]Park-Hah JO, Klemetsdal B, Lysaa R,et al. Thiopurine methyltransferase activity in a Korean population sample in children [J].Clin Pharmacol Ther,1996,60(1): 68.
[10]黄民,姜文奇,刘宇隆,等.中国人与白种人硫唑嘌呤甲基转移酶活性与分布的种族差异[J].癌症,2000,19(10):858.
[11]叶启东,顾龙君,赵金彩,等.上海地区汉族人巯基嘌呤甲基转移酶遗传多态性研究[J].中华医学遗传学杂志,2000,17(6): 421.
[12]Jacqz-Aigrain E, Bessa E, Medard Y,et al.Thiopurine methyltransferase activity in a French population: HPLC assay condition and effects of drugs and inhibitors[J].Br J Clin Pharmacol,1994,38:1.
[13]Weyer N, Fricke L, Iven H,et al. Human thiopurine S-methyltransferase activity in uremia and after renal transplantation [J].Eur J Pharmacol,2001,57:129.
[14]Ekkehard S, Gummert J, Armstrong VM, et al.Azathioprine pharmacogenetics: the relationship between 6-thioguanine nucleotides and thiopurine methyltransferase in patients after heart and kidney transplantation[J].Eur J Clin Chem Clin Biochem,1996, 34: 199.
[15]Rossi AM, Bianchi M, Guarnieri C,et al. Genotype-phenotype correlation for thiopurine S-methyltransferase in healthy Italian subjects[J].Eur J Clin Pharmacol,2001,57:51.
[16]Schmitz G, Aslanidis C, Lackner KJ.Pharmacogenomics:implication for laboratory medicine[J].Clin Chim Acta,2001,308:43.
[17]Hiratsuka M, Inoue T, Omori F,et al. Genetic analysis of thiopurine methyltransferase polymorphism in a Japanese population[J].Mutat Res,2000,448:91.
[18]Krynetski EY, Tai HL, Yates CR,et al. Genetic polymorphism of thiopurine s-methyltransferase: clinical importance and molecular mechanisms[J].Pharmacogenetics,1996,6:279.
[19]Mcleod HL, Coulthard S, Thomas AE, et al. Analysis of thiopurine methyltransferase variant alleles in childhood lymphoblastic leukaemia[J].Bri J Haematol,1999,105:696.