Quantitative adverse outcome pathway modeling for cigarette smoke-inducible airway mucus hypersecretion. Part 2: Bayesian network modeling for probabilistic risk estimation.

IF 3.6 Q2 TOXICOLOGY
Frontiers in toxicology Pub Date : 2025-05-15 eCollection Date: 2025-01-01 DOI:10.3389/ftox.2025.1564864
Shigeaki Ito, Sakuya Ichikawa, Risa Matsumoto, Shugo Muratani, Keigo Sano, Akina Mori, Kazuo Erami
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引用次数: 0

Abstract

The development of in vitro tests that reproduce real-world situations is crucial for toxicity- and disease-risk assessment without animal testing. Because signs and symptoms of health concerns can be complex, it is helpful to create a simplified representation of such manifestations using a conceptual framework such as an adverse outcome pathway (AOP). Combining an AOP with computational models could be a potential tool for the extrapolation of in vitro results to real-world scenarios. Here, we applied Bayesian network-based probabilistic quantitative models for disease-related risk estimation using an in vitro dataset on the AOP of mucus hypersecretion-a known representative symptom of chronic airway disease-obtained by repeated exposure of human bronchial epithelial cells to whole cigarette smoke. We also used a computational aerosol dosimetry model to account for differences between in vitro exposure concentrations and human exposure scenarios. The results revealed dose- and exposure repetition-dependent increases in adverse outcome probability, suggesting that the model reflects the risk continuum of cigarette smoking. Furthermore, under certain assumptions, dosimetry modeling indicated that our in vitro exposure concentrations were similar to actual smoking scenarios. As an exercise, we also calculated in vitro odds ratios for chronic bronchitis that were comparable to the range of real-world odds ratios for chronic bronchitis due to cigarette smoking. Our combinatory risk-assessment approach could be a valuable tool for estimating the chronic inhalation effects of inhalable products and chemicals.

香烟烟雾诱导气道粘液高分泌的定量不良结局通路模型。第2部分:概率风险估计的贝叶斯网络建模。
开发能够再现真实情况的体外试验对于在没有动物试验的情况下进行毒性和疾病风险评估至关重要。由于健康问题的体征和症状可能很复杂,因此使用诸如不良结果通路(AOP)之类的概念框架来创建这种表现的简化表示是有帮助的。将AOP与计算模型相结合可能是将体外结果外推到实际场景的潜在工具。在这里,我们应用基于贝叶斯网络的概率定量模型进行疾病相关风险估计,使用体外数据集来评估黏液分泌过多的AOP——一种已知的慢性气道疾病的代表性症状——通过反复暴露于人类支气管上皮细胞于整个香烟烟雾中获得。我们还使用了计算气溶胶剂量学模型来解释体外暴露浓度和人体暴露情景之间的差异。结果显示,剂量和暴露重复依赖于不良后果概率的增加,表明该模型反映了吸烟的风险连续性。此外,在某些假设下,剂量学模型表明我们的体外暴露浓度与实际吸烟情景相似。作为练习,我们还计算了慢性支气管炎的体外优势比,与吸烟引起的慢性支气管炎的现实世界优势比范围相当。我们的组合风险评估方法可能是估计可吸入产品和化学品的慢性吸入效应的有价值的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.80
自引率
0.00%
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0
审稿时长
13 weeks
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