Incremental effects for continuous exposures

Kyle Schindl, Shuying Shen, Edward H. Kennedy
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Abstract

Causal inference problems often involve continuous treatments, such as dose, duration, or frequency. However, continuous exposures bring many challenges, both with identification and estimation. For example, identifying standard dose-response estimands requires that everyone has some chance of receiving any particular level of the exposure (i.e., positivity). In this work, we explore an alternative approach: rather than estimating dose-response curves, we consider stochastic interventions based on exponentially tilting the treatment distribution by some parameter $\delta$, which we term an incremental effect. This increases or decreases the likelihood a unit receives a given treatment level, and crucially, does not require positivity for identification. We begin by deriving the efficient influence function and semiparametric efficiency bound for these incremental effects under continuous exposures. We then show that estimation of the incremental effect is dependent on the size of the exponential tilt, as measured by $\delta$. In particular, we derive new minimax lower bounds illustrating how the best possible root mean squared error scales with an effective sample size of $n/\delta$, instead of usual sample size $n$. Further, we establish new convergence rates and bounds on the bias of double machine learning-style estimators. Our novel analysis gives a better dependence on $\delta$ compared to standard analyses, by using mixed supremum and $L_2$ norms, instead of just $L_2$ norms from Cauchy-Schwarz bounds. Finally, we show that taking $\delta \to \infty$ gives a new estimator of the dose-response curve at the edge of the support, and we give a detailed study of convergence rates in this regime.
连续暴露的递增效应
因果推断问题通常涉及连续的处理,如剂量、持续时间或频率。然而,连续暴露给识别和估计带来了许多挑战。例如,识别标准剂量-反应估计值要求每个人都有一定的机会接受任何特定水平的暴露(即阳性)。在这项工作中,我们探索了另一种方法:与其估计剂量-反应曲线,不如考虑随机干预,即通过某个参数$\delta$对治疗分布进行指数倾斜,我们称之为增量效应。我们首先推导出连续暴露下这些增量效应的有效影响函数和半参数效率边界。然后,我们证明增量效应的估计取决于指数倾斜的大小,以 $\delta$ 衡量。特别是,我们推导出了新的最小下限,说明了最佳均方根误差是如何与有效样本量 $n/\delta$ 而不是通常样本量 $n$ 成比例的。与标准分析相比,我们的新分析通过使用混合至上和 $L_2$ 准则,而不仅仅是考奇-施瓦茨边界中的 $L_2$ 准则,给出了对 $\delta$ 的更好依赖性。最后,我们证明了将 $\delta \to \infty$取值会在支持边缘给出一个新的剂量-反应曲线估计值,我们还对这一机制中的收敛因子进行了详细研究。
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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