Grant Stephen G
Department of Environmental and Occupational Health, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, USA.
BMC Pediatr. 2005 Jun 29;5:20. doi: 10.1186/1471-2431-5-20.
Induced mutagenesis in utero is likely to have life-long repercussions for the exposed fetus, affecting survival, birth weight and susceptibility to both childhood and adult-onset diseases, such as cancer. In the general population, such exposures are likely to be a consequence of the lifestyle choices of the parents, with exposure to tobacco smoke one of the most pervasive and easily documented. Previous studies attempting to establish a direct link between active smoking and levels of somatic mutation have largely discounted the effects of passive or secondary exposure, and have produced contradictory results.
Data from three studies of possible smoking effects on in utero mutagenesis at the HPRT locus were compiled and reanalyzed, alone and in combination. Where possible, passive exposure to environmental tobacco smoke was considered as a separate category of exposure, rather than being included in the non-smoking controls. Molecular spectra from these studies were reanalyzed after adjustment for reported mutation frequencies from the individual studies and the entire data set.
A series of related studies on mutation at the X-linked HPRT locus in human newborn cord blood samples has led to the novel conclusion that only passive maternal exposure to tobacco mutagens has a significant effect on the developing baby. We performed a pooled analysis of the complete data from these studies, at the levels of both induced mutation frequency and the resulting mutational spectrum.
Our analysis reveals a more commonsensical, yet no less cautionary result: both active maternal smoking and secondary maternal exposure produce quantitatively and qualitatively indistinguishable increases in fetal HPRT mutation. Further, it appears that this effect is not perceptibly ameliorated if the mother adjusts her behavior (i.e. stops smoking) when pregnancy is confirmed, although this conclusion may also be affected by continued passive exposure.
子宫内诱变可能会对受影响的胎儿产生终身影响,影响其存活、出生体重以及对儿童期和成人期疾病(如癌症)的易感性。在普通人群中,此类暴露可能是父母生活方式选择的结果,接触烟草烟雾是最普遍且记录最容易的暴露之一。以往试图建立主动吸烟与体细胞突变水平之间直接联系的研究,很大程度上忽略了被动或二手暴露的影响,且产生了相互矛盾的结果。
收集并重新分析了三项关于吸烟对子宫内HPRT位点诱变可能影响的研究数据,单独分析以及综合分析。在可能的情况下,将被动接触环境烟草烟雾视为一种单独的暴露类别,而非纳入非吸烟对照组。在根据各研究及整个数据集报告的突变频率进行调整后,重新分析了这些研究的分子光谱。
一系列关于人类新生儿脐带血样本中X连锁HPRT位点突变的相关研究得出了一个新结论,即只有母亲被动接触烟草诱变剂才会对发育中的胎儿产生显著影响。我们对这些研究的完整数据在诱导突变频率和由此产生的突变谱水平上进行了汇总分析。
我们的分析揭示了一个更符合常识但同样具有警示意义的结果:母亲主动吸烟和二手暴露都会使胎儿HPRT突变在数量和质量上产生难以区分的增加。此外,即使母亲在确认怀孕后调整行为(即戒烟),这种影响似乎也不会明显减轻,尽管这一结论可能也会受到持续被动暴露的影响。