首页> 外文期刊>Cancer epidemiology, biomarkers and prevention: A publication of the American Association for Cancer Research >The effects of GSTM1 and GSTT1 polymorphisms on micronucleus frequencies in human lymphocytes in vivo.
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The effects of GSTM1 and GSTT1 polymorphisms on micronucleus frequencies in human lymphocytes in vivo.

机译:GSTM1和GSTT1多态性对体内人淋巴细胞微核频率的影响。

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The influence of genetic polymorphisms in GSTM1 and GSTT1 genes on micronucleus frequencies in human peripheral blood lymphocytes was assessed through a pooled analysis of data from seven laboratories that did biomonitoring studies using the in vivo cytokinesis-block micronucleus assay. A total of 301 nonoccupationally exposed individuals (207 males and 94 females) and 343 workers (237 males and 106 females) occupationally exposed to known or suspected genotoxic substances were analyzed by Poisson regression. The results of the pooled analysis indicate that the GSTT1 null subjects had lower micronucleus frequencies than their positive counterparts in the total population (frequency ratio, 0.55; 95% confidence interval, 0.33-0.89). The protective effect of this genotype is reversed with increasing age, with a frequency ratio of 1.33 (95% confidence interval, 1.06-1.68) in subjects aged 60 years. A significant overall increase in micronucleus frequency with age and gender (P < 0.001 and P = 0.024, respectively) was observed, females having higher micronucleus frequencies than males, when occupationally exposed (P = 0.002). Nonoccupationally exposed smokers had lower micronucleus frequencies than nonsmokers (P = 0.001), whereas no significant difference in micronucleus level was observed between smokers and nonsmokers in the occupationally exposed group (P = 0.79). This study confirms that pooled analyses, by increasing the statistical power, are adequate for assessing the involvement of genetic variants on genome stability and for resolving discrepancies among individual studies.
机译:GSTM1和GSTT1基因遗传多态性对人外周血淋巴细胞微核频率的影响是通过对七个实验室的数据进行汇总分析来评估的,这些实验室使用体内胞质阻滞微核试验进行了生物监测研究。通过Poisson回归分析了总共301名非职业接触个人(207例男性和94名女性)和343例工人(237例男性和106例女性)职业性暴露于已知或怀疑的遗传毒性物质。汇总分析的结果表明,在总人群中,GSTT1缺失受试者的微核频率低于阳性受试者(频率比,0.55; 95%置信区间,0.33-0.89)。该基因型的保护作用随着年龄的增长而逆转,在60岁的受试者中频率比为1.33(95%置信区间为1.06-1.68)。随着年龄和性别的增加,微核频率总体上显着增加(分别为P <0.001和P = 0.024),在职业暴露时,女性的微核频率高于男性(P = 0.002)。非职业暴露的吸烟者的微核频率低于非吸烟者(P = 0.001),而职业暴露组的吸烟者与非吸烟者之间的微核水平没有显着差异(P = 0.79)。这项研究证实,通过提高统计能力,合并分析足以评估遗传变异对基因组稳定性的影响并解决各个研究之间的差异。

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