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中国健康儿童硫嘌呤甲基转移酶的表型和基因型研究:汉族与瑶族的比较

Phenotyping and genotyping study of thiopurine S-methyltransferase in healthy Chinese children: a comparison of Han and Yao ethnic groups.

作者信息

Zhang Jian-ping, Guan Yong-yuan, Wu Jue-heng, Xu An-long, Zhou Shufeng, Huang Min

机构信息

Department of Pharmacology, Zhongshan Medical College, Guangzhou 510080, PR China.

出版信息

Br J Clin Pharmacol. 2004 Aug;58(2):163-8. doi: 10.1111/j.1365-2125.2004.02113.x.

Abstract

AIMS

Ethnicity is an important variable influencing drug response. Thiopurine S-methyltransferase (TPMT) plays an important role in the metabolism of thiopurine drugs. Previous population studies have identified ethnic variations in both phenotype and genotype of TPMT, but limited information is available within Chinese population that comprises at least 56 ethnic groups. The current study was conducted to compare both phenotype and genotype of TPMT in healthy Han and Yao Chinese children.

METHODS

TPMT activity was measured in healthy Chinese children by a HPLC assay (n = 213, 87 Han Chinese and 126 Yao Chinese). Allele-specific polymerase chain reaction (PCR) and PCR-restriction fragment length polymorphism (RFLP) were used to determine the frequency of TPMT mutant alleles (TPMT2, TPMT3 A, TPMT3B and TPMT3C) in these children.

RESULTS

There was no significant difference in the mean TPMT activity between Han and Yao Chinese children. A unimodal distribution of TPMT activity in Chinese children was found and the mean TPMT activity was 13.32 +/- 3.49 U ml(-1) RBC. TPMT activity was not found to differ with gender, but tended to increase with age in Yao Chinese children. TPMT2, TPMT3B and TPMT3A were not detected, and only one TPMT3C heterozygote (Han child) was identified in 213 Chinese children. Erythrocyte TPMT activity of this TPMT*3C heterozygote was 12.36 U ml(-1) RBC. The frequency of the known mutant TPMT alleles was 0.2%[1/426] in Chinese children.

CONCLUSION

The frequency distribution of RBC TPMT activity was unimodal. The frequency of the known mutant TPMT alleles in Chinese Children is low and TPMT*3C appears to be the most prevalent among the tested mutant TPMT alleles in this population.

摘要

目的

种族是影响药物反应的一个重要变量。硫嘌呤甲基转移酶(TPMT)在硫嘌呤类药物的代谢中起重要作用。既往人群研究已确定TPMT在表型和基因型方面存在种族差异,但在中国至少包含56个民族的人群中,相关信息有限。本研究旨在比较健康汉族和瑶族中国儿童中TPMT的表型和基因型。

方法

采用高效液相色谱法(HPLC)测定213名健康中国儿童(87名汉族儿童和126名瑶族儿童)的TPMT活性。采用等位基因特异性聚合酶链反应(PCR)和PCR-限制性片段长度多态性(RFLP)方法,确定这些儿童中TPMT突变等位基因(TPMT2、TPMT3A、TPMT3B和TPMT3C)的频率。

结果

汉族和瑶族中国儿童的平均TPMT活性无显著差异。中国儿童的TPMT活性呈单峰分布,平均TPMT活性为13.32±3.49 U ml(-1)红细胞。未发现TPMT活性因性别而异,但瑶族儿童的TPMT活性随年龄增长有升高趋势。未检测到TPMT2、TPMT3B和TPMT3A,在213名中国儿童中仅鉴定出1名TPMT3C杂合子(汉族儿童)。该TPMT*3C杂合子的红细胞TPMT活性为12.36 U ml(-1)红细胞。中国儿童中已知突变TPMT等位基因的频率为0.2%[1/426]。

结论

红细胞TPMT活性的频率分布呈单峰。中国儿童中已知突变TPMT等位基因的频率较低,在该人群中检测到的突变TPMT等位基因中,TPMT*3C似乎最为常见。

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