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Thiopurine methyltransferase phenotypes and genotypes in Brazilians
被引:32
|作者:
Reis, M
[1
]
Santoro, A
[1
]
Suarez-Kurtz, G
[1
]
机构:
[1] Inst Nacl Canc, Coordenacao Pesquisa, Div Farmacol, BR-20231050 Rio De Janeiro, RJ, Brazil
来源:
PHARMACOGENETICS
|
2003年
/
13卷
/
06期
关键词:
TPMT;
genetic polymorphism;
Brazilians;
thiopurines;
D O I:
10.1097/00008571-200306000-00009
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
The polymorphism of thiopurine methyltransferase (TPMT) was studied in 306 healthy Brazilians who were classed, on the basis of self-declared colour and ancestry, as Euro-derived (n = 81), Afro-derived (n = 18) or having interethnic admixture (n = 204). TPMT activity (range 0.17-25.93 U) displayed a trimodal distribution of high (> 11.3 U; 9% of individuals), intermediate (5-11.3 U; 9.8%) and low (0.17 U; 0.3%) phenotypes. The occurrence of the TPMT mutations 238G>C, 460G>A and 719A>G was investigated in all individuals with low or intermediate phenotype, and in 43 with high-activity phenotype. None and two mutant alleles were associated with high- or low-activity phenotypes, respectively, whereas one mutant allele was detected in 26 of the 30 intermediate phenotype individuals. The allele frequencies of TPMT*2, TPMT*3A and TPMT*3C did not differ between individuals classed as Euro-derived (0.76%, 2.03% and 2.54%, respectively) or having interethnic admixture (0.60%, 1.81% and 1.81%, respectively). Furthermore, within each of these groups, the frequencies of TPMT*3A and TPMT*3C were not significantly different. (C) 2003 Lippincott Williams Wilkins.
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页码:371 / 373
页数:3
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