a Regional Center of Nuclear Sciences of the Northeast (CRCN-NE) , Recife , Brazil.
b Department of Genetics, Federal University of Pernambuco , Recife , Brazil.
Int J Radiat Biol. 2019 Aug;95(8):1058-1071. doi: 10.1080/09553002.2019.1607606. Epub 2019 Jun 3.
The goal was to compare the micronucleus (MN) and dicentric plus ring chromosomes (D + R) assays for dose assessment in cases of partial body irradiations (PBI). We constructed calibration curves for each assay at doses ranging from 0 to 5 Gy of X-rays at dose rate of 0.275 Gy/min. To simulate partial-body exposures, blood samples from two donors were irradiated with 0.5, 1, 2 and 4 Gy and the ratios of irradiated to unirradiated blood were 25, 50, and 100%. Different tests were used to confirm if all samples were overdispersed or zero-inflated and for partial-body dose assessment we used the Qdr, Dolphin and Bayesian model. In our samples for D + R calibration curve, practically all doses agreed with Poisson assumption, but MN exhibited overdispersed and zero-inflated cellular distributions. The exact Poisson tests and zero-inflated tests demonstrate that virtually all samples of D + R from PBI simulation fit the Poisson distribution and were not zero-inflated, but the MN samples were also overdispersed and zero-inflated. In the partial-body estimation, when Qdr and Dolphin methods were used the D + R results were better than MN, but the doses estimation defined by the Bayesian methodology were more accurate than the classical methods. Dicentric chromosomes continue to prove to be the best biological marker for dose assessment. However exposure scenarios of partial-body estimation, overdispersion and zero-inflation may not occur, it being a critical point not only for dose assessment, but also to confirm partial-body exposure. MN could be used as alternative assay for partial-body dose estimation, but in case of an accident without any information, the MN assay could not define whether the accident was a whole-body irradiation (WBI) or a PBI.
目的是比较微核(MN)和双着丝粒加环状染色体(D+R)检测在部分身体照射(PBI)中的剂量评估。我们构建了两种检测方法在 X 射线剂量率为 0.275Gy/min,剂量范围从 0 到 5Gy 的校准曲线。为了模拟部分身体照射,从两名供体的血液中照射 0.5、1、2 和 4Gy,并将照射和未照射血液的比例设为 25、50 和 100%。使用不同的测试来确认所有样本是否过度分散或零膨胀,并且使用 Qdr、Dolphin 和贝叶斯模型进行部分身体剂量评估。在我们的 D+R 校准曲线样本中,实际上所有剂量都符合泊松假设,但 MN 表现出过度分散和零膨胀的细胞分布。精确泊松检验和零膨胀检验证明,实际上所有来自 PBI 模拟的 D+R 样本都符合泊松分布且没有零膨胀,但 MN 样本也存在过度分散和零膨胀。在部分身体估计中,当使用 Qdr 和 Dolphin 方法时,D+R 的结果优于 MN,但贝叶斯方法定义的剂量估计比经典方法更准确。双着丝粒染色体继续被证明是剂量评估的最佳生物标志物。然而,部分身体估计、过度分散和零膨胀的暴露场景可能不会发生,这不仅是剂量评估的关键点,也是确认部分身体暴露的关键点。MN 可以用作部分身体剂量估计的替代检测方法,但在没有任何信息的事故情况下,MN 检测方法无法确定事故是全身照射(WBI)还是 PBI。