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首页> 外文期刊>International Journal of Radiation Biology: Covering the Physical, Chemical, Biological, and Medical Effects of Ionizing and Non-ionizing Radiations >Construction of fluorescence in situ hybridization (FISH) translocation dose-response calibration curve with multiple donor data sets using R, based on ISO 20046:2019 recommendations
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Construction of fluorescence in situ hybridization (FISH) translocation dose-response calibration curve with multiple donor data sets using R, based on ISO 20046:2019 recommendations

机译:基于ISO 20046:2019建议,使用r的原位杂交(鱼类)易位剂量 - α易位剂量 - 响应校准曲线的构建

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Purpose: Dose-response curve (DRC) generation is an important aspect in cytogenetic biodosimetry for accurate dose estimation for individuals suspected of prior irradiation. DRC construction with dicentric chromosomes after acute radiation is well-established following the publication of the IAEA EPR-Biodosimetry 2011 and ISO 19238:2014. However, the short half-life of dicentrics might not be suitable for retrospective dose estimation in radiation medical workers, radiation accident clean-up workers and the general public living in areas with higher than average amount of radiation. There is an urgent need for a chromosome translocation-based DRC, which is constructed based on translocation identification with fluorescence in situ hybridization (FISH). Despite several attempts to generate such a DRC in the past 40 years, no internationally standardized protocol has been developed until 2019, resulting in possible statistical uncertainties between DRCs previously generated. Materials and methods: Using the recently published ISO 20049:2019, a DRC from five healthy donors (four males: 23, 35, 44, 55 years old, one female: 33 years old) was generated with age-adjusted translocations scored per cell equivalent (age-adjusted Tr/CE), using a modified R-script previously published in EPR-Biodosimetry, for Co-60 gamma-ray doses of 0, 0.01, 0.02, 0.05, 0.1, 0.2, 0.5 and 1 Gy. The translocation data set used, based on probes used for chromosomes number 1, 2, and 4, was previously published by Abe et al. in 2018. Results: The results output from R include the DRC coefficients (C, alpha, beta), their p-values, the goodness-of-fit Pearson's chi square value and its corresponding p-value, and the DRC with its 95% confidence interval (CI). The equation of the DRC obtained was 0.0005 (+/- 0.0001) +0.0178 (+/- 0.0037) D + 0.0901 (+/- 0.0054) D-2. DRC generated with averaged Tr/CE had a wider 95% CI than DRC generated with pooled Tr/CE, resulting in a 1.3-1.5 times increase in estimated dose range. No outliers between alpha coefficients from previously published modified DRCs and our DRC were detected with robust Z-score. Conclusions: ISO 20046:2019 should be referenced for future FISH translocation-based DRC generation to ensure statistical reliability of dose estimation. Important considerations for FISH translocation-based DRC up to 1 Gy include scoring more than 2000 CE per dose, the use of multiple donors, age-adjustment of observed translocations, the use of a minimum of 5 dose points including 0 Gy, scoring of total simple translocations in only stable cells and the decision of using pooled or averaged age-adjusted Tr/CE.
机译:目的:剂量 - 响应曲线(DRC)生成是细胞遗传学生物渗透细胞中的一个重要方面,用于准确剂量估计疑似疑似辐照的个体。在IAEA EPR-BIODOSIMETRY 2011和ISO 19238:2014的出版后,急性辐射后的DICENTRIC染色体的DRC结构是彻底的。然而,Dicentrics的短暂半衰期可能不适合辐射医疗工作者的回顾性剂量估计,辐射事故清理工人和居住在高于平均辐射量的地区的公众。迫切需要一种基于染色体的易位的DRC,其基于荧光原位杂交(鱼)的易位鉴定构建。尽管有几次尝试在过去的40年内产生这样的DRC,但直到2019年没有制定了国际标准化的议定书,导致了先前产生的DRC之间可能的统计不确定性。材料和方法:使用最近发布的ISO 20049:2019,来自五个健康捐助者的DRC(四个男性:23,35,44,55岁,一名女性:33岁)是由每种细胞的年龄调整的换算产生相当于(年龄调节的TR / CE),使用先前在EPR-BiodosoSimetry中发表的改性R脚本,对于0,0.01,0.02,0.05,0.1,0.2,0.5和1 Gy的Co-60γ射线剂量。使用的基于用于染色体1,2和4的探针的易位数据集先前由Abe等人发布。结果:从R输出的结果包括DRC系数(C,Alpha,Beta),它们的P值,适合的优良皮尔逊的Chi方价及其相应的P值,以及其95的DRC %置信区间(CI)。所得DRC的等式为0.0005(+/- 0.0001)+ 0.0178(+/- 0.0037)D + 0.0901(+/- 0.0054)D-2。使用平均Tr / CE产生的DRC具有比汇集TR / CE产生的DRC更宽的95%CI,导致估计剂量范围增加1.3-1.5倍。通过稳健的Z分数检测来自先前发布的修改的DRC和我们的DRC的Alpha系数之间的异常值。结论:ISO 20046:2019应参考未来的鱼类易位的DRC生成,以确保剂量估计的统计可靠性。基于鱼类易位的DRC的重要考虑因素高达1 GY包括评分2000多剂,使用多种捐赠者,观察到的易位的年龄调整,使用至少5个剂量,包括0 GY,总数仅稳定的细胞中简单的易位以及使用汇集或平均调整后的TR / CE的决定。

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