中华劳动卫生职业病杂志
中華勞動衛生職業病雜誌
중화노동위생직업병잡지
CHINESE JOURNAL OF INDUSTRIAL HYGIENE AND OCCUPATIONAL DISEASES
2011年
1期
20-23
,共4页
黄简抒%张心菊%许笑%关明%周元陵%吕玲%邹和建
黃簡抒%張心菊%許笑%關明%週元陵%呂玲%鄒和建
황간서%장심국%허소%관명%주원릉%려령%추화건
苯%基因表达型%多态性,单核苷酸%白细胞计数
苯%基因錶達型%多態性,單覈苷痠%白細胞計數
분%기인표체형%다태성,단핵감산%백세포계수
Benzene%Gene expression profiling%Polymorphism,single mucleotide%Leuk ocyte count
目的 探讨MDR1 C3435T对苯作业人员外周血白细胞(WBC)计数的影响.方法 检测121例苯作业人员和110例正常对照组MDR1基因的多态性,并对苯作业人员中携带不同基因型个体的WBC计数进行比较.结果 对照组MDR1 3435 C/C基因型分布频率为37.27%,C/T基因型为46.36%,T/T基因型为16.37%;接触组C/C基因型分布频率为38.84%,C/T基因型为41.33%,T/T基因型为19.83%,两组比较,差异无统计学意义(P=0.686).接触组携带T/T基因型者WBC计数为(5.46±1.51)×109/L,明显低于携带C/C+C/T基因型者[WBC计数为(6.08±1.28)×109/L],差异有统计学意义(P=0.044).结论 苯血液系统毒作用机制中可能涉及多药耐药基因编码产物P-糖蛋白的参与,携带MDR1 3435T/T基因型个体接触苯,可增高中毒风险.
目的 探討MDR1 C3435T對苯作業人員外週血白細胞(WBC)計數的影響.方法 檢測121例苯作業人員和110例正常對照組MDR1基因的多態性,併對苯作業人員中攜帶不同基因型箇體的WBC計數進行比較.結果 對照組MDR1 3435 C/C基因型分佈頻率為37.27%,C/T基因型為46.36%,T/T基因型為16.37%;接觸組C/C基因型分佈頻率為38.84%,C/T基因型為41.33%,T/T基因型為19.83%,兩組比較,差異無統計學意義(P=0.686).接觸組攜帶T/T基因型者WBC計數為(5.46±1.51)×109/L,明顯低于攜帶C/C+C/T基因型者[WBC計數為(6.08±1.28)×109/L],差異有統計學意義(P=0.044).結論 苯血液繫統毒作用機製中可能涉及多藥耐藥基因編碼產物P-糖蛋白的參與,攜帶MDR1 3435T/T基因型箇體接觸苯,可增高中毒風險.
목적 탐토MDR1 C3435T대분작업인원외주혈백세포(WBC)계수적영향.방법 검측121례분작업인원화110례정상대조조MDR1기인적다태성,병대분작업인원중휴대불동기인형개체적WBC계수진행비교.결과 대조조MDR1 3435 C/C기인형분포빈솔위37.27%,C/T기인형위46.36%,T/T기인형위16.37%;접촉조C/C기인형분포빈솔위38.84%,C/T기인형위41.33%,T/T기인형위19.83%,량조비교,차이무통계학의의(P=0.686).접촉조휴대T/T기인형자WBC계수위(5.46±1.51)×109/L,명현저우휴대C/C+C/T기인형자[WBC계수위(6.08±1.28)×109/L],차이유통계학의의(P=0.044).결론 분혈액계통독작용궤제중가능섭급다약내약기인편마산물P-당단백적삼여,휴대MDR1 3435T/T기인형개체접촉분,가증고중독풍험.
Objective To explore the effects of MDR1 C3435T on the peripheral white blood cell counts in workers exposed to benzene. Methods One hundred and twenty-one benzene-exposed workers and 110 healthy controls without benzene exposure were enrolled in this study. White blood cell counts influenced by the polymorphism of MDR1 gene were analyzed. Results The frequency of MDR1 3435 C/C, C/T, T/T in healthy controls was 37.27%, 46.36%, 16.37%, respectively,and it was 38.84%, 41.33%, 19.83% in the benzene-exposed workers, respectively. The frequency of the MDR1 gene was also not significantly different between benzene exposed workers and controls. Subjects exposed to benzene with MDR1 3435 mutation genotype (T/T) had the significantly lower WBC[(5.46±1.51 )×109/L] than those carrying wild type(C/C) and heterozygous (C/T), whose WBC were (6.08±1.28)×109/L(P=0.044). Conclusion P-glycoprotein encoded by MDR1 gene may be implicated into the hematotoxicity of benzene. Subjects carrying MDR1 3435 T/T genotype may have a higher risk of benzene poisoning.