Causal bounds for outcome-dependent sampling in observational studies
Erin E. Gabriel, Michael C. Sachs, Arvid Sjölander
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36 pages, 3 figures. Update to include revisions after peer review. In Press at the Journal of the American Statistical Association, Theory and methods
Outcome-dependent sampling designs are common in many different scientific fields including epidemiology, ecology, and economics. As with all observational studies, such designs often suffer from unmeasured confounding, which generally precludes the nonparametric identification of causal effects. Nonparametric bounds can provide a way to narrow the range of possible values for a nonidentifiable causal effect without making additional untestable assumptions. The nonparametric bounds literature has almost exclusively focused on settings with random sampling, and the bounds have often been derived with a particular linear programming method. We derive novel bounds for the causal risk difference, often referred to as the average treatment effect, in six settings with outcome-dependent sampling and unmeasured confounding for a binary outcome and exposure. Our derivations of the bounds illustrate two approaches that may be applicable in other settings where the bounding problem cannot be directly stated as a system of linear constraints. We illustrate our derived bounds in a real data example involving the effect of vitamin D concentration on mortality.
Despite the major advances taken in causal modeling, causality is still an unfamiliar topic for many statisticians. In this paper, it is demonstrated from the beginning to the end how causal effects can be estimated from observational data assuming that the causal structure is known. To make the problem more challenging, the causal effects are highly nonlinear and the data are missing at random. The tools used in the estimation include causal models with design, causal calculus, multiple imputation and generalized additive models. The main message is that a trained statistician can estimate ca…
A framework for causal inference from two-level factorial designs is proposed. The framework utilizes the concept of potential outcomes that lies at the center stage of causal inference and extends Neyman's repeated sampling approach for estimation of causal effects and randomization tests based on Fisher's sharp null hypothesis to the case of 2-level factorial experiments. The framework allows for statistical inference from a finite population, permits definition and estimation of estimands other than "average factorial effects" and leads to more flexible inference procedures than those based…
Rejoinder on Causal Inference Through Potential Outcomes and Principal Stratification: Application to Studies with ``Censoring'' Due to Death by D. B. Rubin [math.ST/0612783]
Causal effects may vary among individuals and can even be of opposite signs. When significant effect heterogeneity exists, the population average causal effect might be uninformative for an individual. Due to the fundamental problem of causality, individual causal effects (ICEs) cannot be retrieved from cross-sectional data. However, in crossover studies, it is accepted that ICEs can be estimated under the assumptions of no carryover effects and time invariance of potential outcomes. A generic potential-outcome formulation with appropriate statistical assumptions to identify ICEs is lacking fo…
Causal inference on multiple non-independent outcomes raises serious challenges, because multivariate techniques that properly account for the outcome's dependence structure need to be considered. We focus on the case of binary outcomes framing our discussion in the potential outcome approach to causal inference. We define causal effects of treatment on joint outcomes introducing the notion of product outcomes. We also discuss a decomposition of the causal effect on product outcomes into intrinsic and extrinsic causal effects, which respectively provide information on treatment effect on the i…
The literature for count modeling provides useful tools to conduct causal inference when outcomes take non-negative integer values. Applied to the potential outcomes framework, we link the Bayesian causal inference literature to statistical models for count data. We discuss the general architectural considerations for constructing the predictive posterior of the missing potential outcomes. Special considerations for estimating average treatment effects are discussed, some generalizing certain relationships and some not yet encountered in the causal inference literature.
School of Computer Science, University of Birmingham(伯明翰大学计算机学院);MIT(麻省理工学院)
To draw scientifically meaningful conclusions and build reliable models of quantitative phenomena, cause and effect must be taken into consideration (either implicitly or explicitly). This is particularly challenging when the measurements are not from controlled experimental (interventional) settings, since cause and effect can be obscured by spurious, indirect influences. Modern predictive techniques from machine learning are capable of capturing high-dimensional, nonlinear relationships between variables while relying on few parametric or probabilistic model assumptions. However, since these…
What is the ideal regression (if any) for estimating average causal effects? We study this question in the setting of discrete covariates, deriving expressions for the finite-sample variance of various stratification estimators. This approach clarifies the fundamental statistical phenomena underlying many widely-cited results. Our exposition combines insights from three distinct methodological traditions for studying causal effect estimation: potential outcomes, causal diagrams, and structural models with additive errors.
Several approaches to causal inference from observational studies have been proposed. Since the proposal of Rubin (1974) many works have developed a counterfactual approach to causality, statistically formalized by potential outcomes. Pearl (2000) has put forward a theory of structural causal models which gives an important role to graphical models and do not necessarily use potential outcomes. On the other hand, several authors have developed a dynamical approach in line with Granger (1969). We analyze prospective and retrospective causal questions and their different modalities. Following Da…
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Many outcomes of interest in the social and health sciences, as well as in modern applications in computational social science and experimentation on social media platforms, are ordinal and do not have a meaningful scale. Causal analyses that leverage this type of data, termed ordinal non-numeric, require careful treatment, as much of the classical potential outcomes literature is concerned with estimation and hypothesis testing for outcomes whose relative magnitudes are well defined. Here, we propose a class of finite population causal estimands that depend on conditional distributions of the…
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Unobserved confounding presents a major threat to causal inference from observational studies. Recently, several authors suggest that this problem may be overcome in a shared confounding setting where multiple treatments are independent given a common latent confounder. It has been shown that under a linear Gaussian model for the treatments, the causal effect is not identifiable without parametric assumptions on the outcome model. In this paper, we show that the causal effect is indeed identifiable if we assume a general binary choice model for the outcome with a non-probit link. Our identific…
Causal inference is best understood using potential outcomes. This use is particularly important in more complex settings, that is, observational studies or randomized experiments with complications such as noncompliance. The topic of this lecture, the issue of estimating the causal effect of a treatment on a primary outcome that is ``censored'' by death, is another such complication. For example, suppose that we wish to estimate the effect of a new drug on Quality of Life (QOL) in a randomized experiment, where some of the patients die before the time designated for their QOL to be assessed. …
Analyses of biomedical studies often necessitate modeling longitudinal causal effects. The current focus on personalized medicine and effect heterogeneity makes this task even more challenging. Towards this end, structural nested mean models (SNMMs) are fundamental tools for studying heterogeneous treatment effects in longitudinal studies. However, when outcomes are binary, current methods for estimating multiplicative and additive SNMM parameters suffer from variation dependence between the causal parameters and the non-causal nuisance parameters. This leads to a series of difficulties in int…
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Noncompliance and missing data often occur in randomized trials, which complicate the inference of causal effects. When both noncompliance and missing data are present, previous papers proposed moment and maximum likelihood estimators for binary and normally distributed continuous outcomes under the latent ignorable missing data mechanism. However, the latent ignorable missing data mechanism may be violated in practice, because the missing data mechanism may depend directly on the missing outcome itself. Under noncompliance and an outcome-dependent nonignorable missing data mechanism, previous…
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In medical research, a scenario often entertained is randomized controlled $2^2$ factorial design with a binary outcome. By utilizing the concept of potential outcomes, Dasgupta et al. (2015) proposed a randomization-based causal inference framework, allowing flexible and simultaneous estimations and inferences of the factorial effects. However, a fundamental challenge that Dasgupta et al. (2015)'s proposed methodology faces is that the sampling variance of the randomization-based factorial effect estimator is unidentifiable, rendering the corresponding classic "Neymanian" variance estimator s…