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Contrasting Theories of Interaction in Epidemiology and Toxicology

机译:流行病学和毒理学中相互作用的相反理论

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摘要

Background: Epidemiologists and toxicologists face similar problems when assessing interactions between exposures, yet they approach the question very differently. The epidemiologic definition of “interaction” leads to the additivity of risk differences (RDA) as the fundamental criterion for causal inference about biological interactions. Toxicologists define “interaction” as departure from a model based on mode of action: concentration addition (CA; for similarly acting compounds) or independent action (IA; for compounds that act differently).Objectives: We compared and contrasted theoretical frameworks for interaction in the two fields.Methods: The same simple thought experiment has been used in both both epidemiology and toxicology to develop the definition of “noninteraction,” with nearly opposite interpretations. In epidemiology, the “sham combination” leads to a requirement that noninteractive dose–response curves be linear, whereas in toxicology, it results in the model of CA. We applied epidemiologic tools to mathematical models of concentration-additive combinations to evaluate their utility.Results: RDA is equivalent to CA only for linear dose–response curves. Simple models demonstrate that concentration-additive combinations can result in strong synergy or antagonism in the epidemiologic framework at even the lowest exposure levels. For combinations acting through nonsimilar pathways, RDA approximates IA at low effect levels.Conclusions: Epidemiologists have argued for a single logically consistent definition of interaction, but the toxicologic perspective would consider this approach less biologically informative than a comparison with CA or IA. We suggest methods for analysis of concentration-additive epidemiologic data. The two fields can learn a great deal about interaction from each other.
机译:背景:流行病学家和毒理学家在评估暴露之间的相互作用时面临类似的问题,但是他们对这个问题的看法却大不相同。 “相互作用”的流行病学定义导致风险差异(RDA)的加和,这是对生物学相互作用进行因果推理的基本标准。毒理学家将“相互作用”定义为基于作用模式的模型偏离:浓度增加(CA;作用相似的化合物)或独立作用(IA;作用不同的化合物)。目的:我们比较并对比了相互作用的理论框架方法:在流行病学和毒理学上都使用了相同的简单思想实验来开发“非相互作用”的定义,其解释几乎相反。在流行病学中,“假组合”导致要求非交互式剂量反应曲线是线性的,而在毒理学中,它导致了CA模型。我们将流行病学工具应用于浓度加法组合的数学模型以评估其效用。结果:对于线性剂量反应曲线,RDA等效于CA。简单的模型表明,浓度-添加剂组合即使在最低暴露水平下也可以在流行病学框架中产生强大的协同作用或拮抗作用。对于通过非相似途径起作用的组合,RDA在较低的作用水平下近似于IA。我们建议分析浓度相加的流行病学数据的方法。这两个领域可以相互学习很多。

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