首页 | 本学科首页   官方微博 | 高级检索  
检索        

细胞色素P450 1A1和2D6基因多态性与慢性苯中毒的危险性
引用本文:顾寿永,张忠彬,曹多志,万俊香,高晓玲,金锡鹏,夏昭林.细胞色素P450 1A1和2D6基因多态性与慢性苯中毒的危险性[J].中华劳动卫生职业病杂志,2006,24(5):266-269.
作者姓名:顾寿永  张忠彬  曹多志  万俊香  高晓玲  金锡鹏  夏昭林
作者单位:1. 200032,上海,复旦大学公共卫生学院劳动卫生教研室
2. 马鞍山钢铁公司医院劳动卫生研究所
3. 上海市第一人民医院
基金项目:国家自然科学基金资助项目(30271113),国家科技部“973”项目(2002CB512902)
摘    要:目的 探讨细胞色素P450 1A1和2D6基因多态性与慢性苯中毒易感性的关系.方法 采用病例-对照研究,选择152名苯中毒工人为病例组,152名接触苯而无中毒表现的工人为对照组.采用限制性片段聚合酶链反应(PCR-RFLP)技术检测CYP1A1基因3'端非编码区MspⅠ和CYP2D6第1外显子c.188位点、g.212位点多态性.结果 携带CYP1A1 MspⅠT/T基因型的个体发生苯中毒的危险性是携带有CYP1A1 Msp Ⅰ T/C或C/C基因型的个体的1.32倍(95%CI:1.05~1.65,P=0.02);在不吸烟的人群中,携带CYP1A1 MspⅠ T/T基因型的个体发生苯中毒的风险性是携带T/C或C/C基因型的个体的1.56倍(95%CI:1.15~2.12,P=0.003);携带有CYP2D6 c.188 C/C或C/T基因型个体发生苯中毒的危险性是携带有CYP2D6 c.188 T/T基因型的个体的1.23倍(95%CI:1.05~1.42,P=0.01),在不吸烟的人群中,携带CYP2D6 c.188 C/C或C/T基因型个体发生苯中毒的危险性是携带有CYP2D6 c.188 T/T基因型的个体的1.23倍(95%CI:1.04~1.47,P=0.01).未发现研究对象的CYP2D6g.212位点存在多态性.结论 携带CYP1A1 Msp ⅠT/T基因型、CYP2D6 c.188 C/C和C/T基因型个体对苯中毒可能易感.

关 键 词:苯中毒  多态性基因  生活方式
修稿时间:2005年2月4日

Genetic polymorphism of CYP-1A1, CYP2D6 and risks of chronic benzene poisoning
GU Shou-yong,ZHANG Zhong-bin,CAO Duo-zhi,WAN Jun-xiang,GAO Xiao-ling,IN Xi-peng,XIA Zhao-lin.Genetic polymorphism of CYP-1A1, CYP2D6 and risks of chronic benzene poisoning[J].Chinese Journal of Industrial Hygiene and Occupational Diseases,2006,24(5):266-269.
Authors:GU Shou-yong  ZHANG Zhong-bin  CAO Duo-zhi  WAN Jun-xiang  GAO Xiao-ling  IN Xi-peng  XIA Zhao-lin
Institution:Department of Occupational Health, School of Public Health, Fudan University, Shanghai 200032, China.
Abstract:Objective To explore the relationship between genetic polymorphisms of CYP-1A1 and CYP2D6 and risks of chronic benzene poisoning(BP). Methods A case control study was conducted. 152 BP patients and 152 workers occupationally exposed to benzene without poisoning manifestations were involved. Polymerase chain reaction followed by restriction fragment length polymorphism(PCR-RFLP) technology was used for detecting the single nucleotide polymorphisms(SNPs)of Msp I in the non-coding region of CYP-1A1 gene and c . 188 ,g .212 position in the first extron of CYP2D6 gene. Results The individuals with CYP1A1 Msp I T/T genotype had a 1 .32 times(95% CI: 1.05 ~ 1.65, P = 0.02) increased risk of BP compared with those carrying T/C and C/C genotypes.In no-smoking population, there was a 1.56 times(95% CI: 1 .15 ~ 2.12, P = 0.003)increased risk of BP for subjects carrying CYP1A1 Msp I T/T genotype compared with those carrying T/C and C/C genotypes. The individuals carrying CYP2D6c. 188 C/C or C/T genotype had a 1 .23 times(95% CI: 1 .05 ~ 1.42, P = 0.01 )in-creased risk compared with those carrying T/T genotypes.In no-smoking population,there was a 1.23 times(95% CI: 1.04- 1.47, P = 0.01 )increased risk of BP for subjects carrying CYP2D6c.188 C/C or C/T genotypes compared with those carrying T/T genotype. The single nucleotide polymorphism of g. 212 position in the first extron of CYP2D6 gene had not been validated. Conclusion The individuals with CYP2D6 c. 188 C/C, CYP2D6 c. 188 C/T and CYP1AI Msp I T/T genotypes tend to be more susceptible to benzene toxicity.
Keywords:Benzene poisoning  Genetic polymorphism  Life style
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号