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An updated weight of the evidence evaluation of reproductive and developmental effects of low doses of bisphenol A

机译:低剂量双酚A对生殖和发育影响的证据评估的最新权重

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There is controversy over whether low doses of bisphenol A (BPA, CAS no. 80-05-7) cause reproductive and developmental effects in humans. We update the 2004 weight-of-evidence assessment of an expert panel convened by Harvard's Center for Risk Analysis by critically evaluating over 50 additional studies published between April 2002 and February 2006 that examine in vivo reproductive and developmental toxicity in mammals at doses <= 5 mg/kg-d. Our findings are consistent with the Harvard study: some statistically significant findings in rats and mice exist but they are generally countered by more numerous studies showing no effect for similar endpoints. No effect is marked or consistent across species, doses, and time points. Some mouse studies report morphological changes in testes and sperm and some non-oral mouse studies report morphological changes in female reproductive organs. Owing to lack of first-pass metabolism, results from non-oral studies are of limited relevance to oral human exposure. Human biomonitoring indicates exposures lower than the "low doses in the reviewed animal studies. Reports of human health impact are very limited and inconsistent. Taken together, the weight of evidence does not support the hypothesis that low oral doses of BPA adversely affect human reproductive and developmental health.
机译:关于低剂量的双酚A(BPA,CAS号80-05-7)是否会在人类中引起生殖和发育影响,存在争议。我们通过对2002年4月至2006年2月间发表的50项其他研究进行严格评估,更新了由哈佛大学风险分析中心召集的专家小组的2004年证据权重评估,这些研究检查了剂量小于等于5的哺乳动物体内的生殖和发育毒性毫克/千克·天我们的发现与哈佛大学的研究一致:在大鼠和小鼠中存在一些统计学上显着的发现,但通常被更多的研究抵销,这些研究表明对相似的终点没有影响。在物种,剂量和时间点上没有明显或一致的影响。一些小鼠研究报告了睾丸和精子的形态变化,一些非口服小鼠研究报告了女性生殖器官的形态变化。由于缺乏首过代谢,非口服研究的结果与人类口服接触的相关性有限。人体生物监测表明暴露低于“低剂量”。有关人类健康影响的报告非常有限且不一致。综合来看,证据量不足以支持低口服BPA剂量会对人体生殖器官和健康产生不利影响的假说。发育健康。

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