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利用辐射效应的机制数学模型加强低剂量风险评估。

Enhancing low-dose risk assessment using mechanistic mathematical models of radiation effects.

作者信息

Shuryak Igor

机构信息

Center for Radiological Research, Columbia University, New York, NY, United States of America.

出版信息

J Radiol Prot. 2019 Jul 11;39(4):S1-S13. doi: 10.1088/1361-6498/ab3101.

Abstract

Mechanistic mathematical modeling of ionizing radiation (IR) effects has a long history spanning several decades. Models that mathematically represent current knowledge and hypotheses about how radiation damages cells and organs, leading to deleterious outcomes such as carcinogenesis, are particularly useful for estimating radiation risks at doses that are relevant for radiation protection, but are too low to provide a strong 'signal-to-noise ratio' in epidemiological or experimental studies with realistic sample sizes. Here, I discuss examples of models in several relevant areas, including radionuclide biokinetics, non-targeted IR effects, DNA double-strand break (DSB) rejoining and radiation carcinogenesis. I do not provide a detailed review of the vast modeling literature in these fields, but focus on concepts that we have implemented, such as using continuous probability distributions of exponential rates to model radionuclide biokinetics and DSB rejoining, and combining short and long time scales in carcinogenesis models. Improvements in models, including the ability to generate new hypotheses based on model predictions, may come from the introduction of additional novel concepts and from integrating multiple data types.

摘要

电离辐射(IR)效应的机制数学建模有着跨越数十年的悠久历史。那些用数学方法表示当前关于辐射如何损伤细胞和器官从而导致诸如致癌等有害后果的知识和假设的模型,对于估算与辐射防护相关剂量下的辐射风险尤为有用,这些剂量过低,以至于在具有实际样本量的流行病学或实验研究中无法提供强大的“信噪比”。在此,我将讨论几个相关领域的模型示例,包括放射性核素生物动力学、非靶向IR效应、DNA双链断裂(DSB)重新连接以及辐射致癌作用。我不会对这些领域中大量的建模文献进行详细综述,而是聚焦于我们已实施的概念,比如使用指数率的连续概率分布来模拟放射性核素生物动力学和DSB重新连接,以及在致癌模型中结合短时间尺度和长时间尺度。模型的改进,包括基于模型预测生成新假设的能力,可能源于引入更多新颖概念以及整合多种数据类型。

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