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Wang Miao

Publications and source records attributed to Wang Miao.

At least 37 records · Page 2Linked to original sources

Doubly Robust Proximal Synthetic Controls

To infer the treatment effect for a single treated unit using panel data, synthetic control methods construct a linear combination of control units' outcomes that mimics the treated unit's pre-treatment outcome trajectory. This linear combination is subsequently used to impute the counterfactual outcomes of the treated unit had it not been treated in the post-treatment period, and used to estimate the treatment effect. Existing synthetic control methods rely on correctly modeling certain aspects of the counterfactual outcome generating mechanism and may require near-perfect matching of the pre-treatment trajectory. Inspired by proximal causal inference, we obtain two novel nonparametric identifying formulas for the average treatment effect for the treated unit: one is based on weighting, and the other combines models for the counterfactual outcome and the weighting function. We introduce the concept of covariate shift to synthetic controls to obtain these identification results conditional on the treatment assignment. We also develop two treatment effect estimators based on these two formulas and the generalized method of moments. One new estimator is doubly robust: it is consistent and asymptotically normal if at least one of the outcome and weighting models is correctly specified. We demonstrate the performance of the methods via simulations and apply them to evaluate the effectiveness of a Pneumococcal conjugate vaccine on the risk of all-cause pneumonia in Brazil.

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NAS-ASDet: An Adaptive Design Method for Surface Defect Detection Network using Neural Architecture Search

Deep convolutional neural networks (CNNs) have been widely used in surface defect detection. However, no CNN architecture is suitable for all detection tasks and designing effective task-specific requires considerable effort. The neural architecture search (NAS) technology makes it possible to automatically generate adaptive data-driven networks. Here, we propose a new method called NAS-ASDet to adaptively design network for surface defect detection. First, a refined and industry-appropriate search space that can adaptively adjust the feature distribution is designed, which consists of repeatedly stacked basic novel cells with searchable attention operations. Then, a progressive search strategy with a deep supervision mechanism is used to explore the search space faster and better. This method can design high-performance and lightweight defect detection networks with data scarcity in industrial scenarios. The experimental results on four datasets demonstrate that the proposed method achieves superior performance and a relatively lighter model size compared to other competitive methods, including both manual and NAS-based approaches.

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Proximal Causal Inference without Uniqueness Assumptions

We consider identification and inference about a counterfactual outcome mean when there is unmeasured confounding using tools from proximal causal inference (Miao et al. [2018], Tchetgen Tchetgen et al. [2020]). Proximal causal inference requires existence of solutions to at least one of two integral equations. We motivate the existence of solutions to the integral equations from proximal causal inference by demonstrating that, assuming the existence of a solution to one of the integral equations, $\sqrt{n}$-estimability of a linear functional (such as its mean) of that solution requires the existence of a solution to the other integral equation. Solutions to the integral equations may not be unique, which complicates estimation and inference. We construct a consistent estimator for the solution set for one of the integral equations and then adapt the theory of extremum estimators to find from the estimated set a consistent estimator for a uniquely defined solution. A debiased estimator for the counterfactual mean is shown to be root-$n$ consistent, regular, and asymptotically semiparametrically locally efficient under additional regularity conditions.

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Double Negative Control Inference in Test-Negative Design Studies of Vaccine Effectiveness

The test-negative design (TND) has become a standard approach to evaluate vaccine effectiveness against the risk of acquiring infectious diseases in real-world settings, such as Influenza, Rotavirus, Dengue fever, and more recently COVID-19. In a TND study, individuals who experience symptoms and seek care are recruited and tested for the infectious disease which defines cases and controls. Despite TND's potential to reduce unobserved differences in healthcare seeking behavior (HSB) between vaccinated and unvaccinated subjects, it remains subject to various potential biases. First, residual confounding may remain due to unobserved HSB, occupation as healthcare worker, or previous infection history. Second, because selection into the TND sample is a common consequence of infection and HSB, collider stratification bias may exist when conditioning the analysis on tested samples, which further induces confounding by latent HSB. In this paper, we present a novel approach to identify and estimate vaccine effectiveness in the target population by carefully leveraging a pair of negative control exposure and outcome variables to account for potential hidden bias in TND studies. We illustrate our proposed method with extensive simulations and an application to study COVID-19 vaccine effectiveness using data from the University of Michigan Health System.

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Semiparametric proximal causal inference

Skepticism about the assumption of no unmeasured confounding, also known as exchangeability, is often warranted in making causal inferences from observational data; because exchangeability hinges on an investigator's ability to accurately measure covariates that capture all potential sources of confounding. In practice, the most one can hope for is that covariate measurements are at best proxies of the true underlying confounding mechanism operating in a given observational study. In this paper, we consider the framework of proximal causal inference introduced by Miao et al. (2018); Tchetgen Tchetgen et al. (2020), which while explicitly acknowledging covariate measurements as imperfect proxies of confounding mechanisms, offers an opportunity to learn about causal effects in settings where exchangeability on the basis of measured covariates fails. We make a number of contributions to proximal inference including (i) an alternative set of conditions for nonparametric proximal identification of the average treatment effect; (ii) general semiparametric theory for proximal estimation of the average treatment effect including efficiency bounds for key semiparametric models of interest; (iii) a characterization of proximal doubly robust and locally efficient estimators of the average treatment effect. Moreover, we provide analogous identification and efficiency results for the average treatment effect on the treated. Our approach is illustrated via simulation studies and a data application on evaluating the effectiveness of right heart catheterization in the intensive care unit of critically ill patients.

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Theory for identification and Inference with Synthetic Controls: A Proximal Causal Inference Framework

Synthetic control (SC) methods are commonly used to estimate the treatment effect on a single treated unit in panel data settings. An SC is a weighted average of control units built to match the treated unit, with weights typically estimated by regressing (summaries of) pre-treatment outcomes and measured covariates of the treated unit to those of the control units. However, it has been established that in the absence of a good fit, such regression estimator will generally perform poorly. In this paper, we introduce a proximal causal inference framework to formalize identification and inference for both the SC and ultimately the treatment effect on the treated, based on the observation that control units not contributing to the construction of an SC can be repurposed as proxies of latent confounders. We view the difference in the post-treatment outcomes between the treated unit and the SC as a time series, which opens the door to various time series methods for treatment effect estimation. The proposed framework can accommodate nonlinear models, which allows for binary and count outcomes that are understudied in the SC literature. We illustrate with simulation studies and an application to evaluation of the 1990 German Reunification.

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A robust fusion-extraction procedure with summary statistics in the presence of biased sources

Information from various data sources is increasingly available nowadays. However, some of the data sources may produce biased estimation due to commonly encountered biased sampling, population heterogeneity, or model misspecification. This calls for statistical methods to combine information in the presence of biased sources. In this paper, a robust data fusion-extraction method is proposed. The method can produce a consistent estimator of the parameter of interest even if many of the data sources are biased. The proposed estimator is easy to compute and only employs summary statistics, and hence can be applied to many different fields, e.g. meta-analysis, Mendelian randomisation and distributed system. Moreover, the proposed estimator is asymptotically equivalent to the oracle estimator that only uses data from unbiased sources under some mild conditions. Asymptotic normality of the proposed estimator is also established. In contrast to the existing meta-analysis methods, the theoretical properties are guaranteed even if both the number of data sources and the dimension of the parameter diverge as the sample size increases, which ensures the performance of the proposed method over a wide range. The robustness and oracle property is also evaluated via simulation studies. The proposed method is applied to a meta-analysis data set to evaluate the surgical treatment for the moderate periodontal disease, and a Mendelian randomization data set to study the risk factors of head and neck cancer.

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A self-censoring model for multivariate nonignorable nonmonotone missing data

We introduce a self-censoring model for multivariate nonignorable nonmonotone missing data, where the missingness process of each outcome is affected by its own value and is associated with missingness indicators of other outcomes, while conditionally independent of the other outcomes. The self-censoring model complements previous graphical approaches for the analysis of multivariate nonignorable missing data. It is identified under a completeness condition stating that any variability in one outcome can be captured by variability in the other outcomes among complete cases. For estimation, we propose a suite of semiparametric estimators including doubly robust estimators that deliver valid inferences under partial misspecification of the full-data distribution. We evaluate the performance of the proposed estimators with simulations and apply them to analyze a study about the effect of highly active antiretroviral therapy on preterm delivery of HIV-positive mothers.

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Sharp bounds for variance of treatment effect estimators in the finite population in the presence of covariates

In a completely randomized experiment, the variances of treatment effect estimators in the finite population are usually not identifiable and hence not estimable. Although some estimable bounds of the variances have been established in the literature, few of them are derived in the presence of covariates. In this paper, the difference-in-means estimator and the Wald estimator are considered in the completely randomized experiment with perfect compliance and noncompliance, respectively. Sharp bounds for the variances of these two estimators are established when covariates are available. Furthermore, consistent estimators for such bounds are obtained, which can be used to shorten the confidence intervals and improve the power of tests. Confidence intervals are constructed based on the consistent estimators of the upper bounds, whose coverage rates are uniformly asymptotically guaranteed. Simulations were conducted to evaluate the proposed methods. The proposed methods are also illustrated with two real data analyses.

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Proximal Causal Inference for Complex Longitudinal Studies

A standard assumption for causal inference about the joint effects of time-varying treatment is that one has measured sufficient covariates to ensure that within covariate strata, subjects are exchangeable across observed treatment values, also known as "sequential randomization assumption (SRA)". SRA is often criticized as it requires one to accurately measure all confounders. Realistically, measured covariates can rarely capture all confounders with certainty. Often covariate measurements are at best proxies of confounders, thus invalidating inferences under SRA. In this paper, we extend the proximal causal inference (PCI) framework of Miao et al. (2018) to the longitudinal setting under a semiparametric marginal structural mean model (MSMM). PCI offers an opportunity to learn about joint causal effects in settings where SRA based on measured time-varying covariates fails, by formally accounting for the covariate measurements as imperfect proxies of underlying confounding mechanisms. We establish nonparametric identification with a pair of time-varying proxies and provide a corresponding characterization of regular and asymptotically linear estimators of the parameter indexing the MSMM, including a rich class of doubly robust estimators, and establish the corresponding semiparametric efficiency bound for the MSMM. Extensive simulation studies and a data application illustrate the finite sample behavior of proposed methods.

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Doubly Robust Proximal Causal Inference under Confounded Outcome-Dependent Sampling

Unmeasured confounding and selection bias are often of concern in observational studies and may invalidate a causal analysis if not appropriately accounted for. Under outcome-dependent sampling, a latent factor that has causal effects on the treatment, outcome, and sample selection process may cause both unmeasured confounding and selection bias, rendering standard causal parameters unidentifiable without additional assumptions. Under an odds ratio model for the treatment effect, Li et al. 2022 established both proximal identification and estimation of causal effects by leveraging a pair of negative control variables as proxies of latent factors at the source of both confounding and selection bias. However, their approach relies exclusively on the existence and correct specification of a so-called treatment confounding bridge function, a model that restricts the treatment assignment mechanism. In this article, we propose doubly robust estimation under the odds ratio model with respect to two nuisance functions -- a treatment confounding bridge function and an outcome confounding bridge function that restricts the outcome law, such that our estimator is consistent and asymptotically normal if either bridge function model is correctly specified, without knowing which one is. Thus, our proposed doubly robust estimator is potentially more robust than that of Li et al. 2022. Our simulations confirm that the proposed proximal estimators of an odds ratio causal effect can adequately account for both residual confounding and selection bias under stated conditions with well-calibrated confidence intervals in a wide range of scenarios, where standard methods generally fail to be consistent. In addition, the proposed doubly robust estimator is consistent if at least one confounding bridge function is correctly specified.

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A Selective Review of Negative Control Methods in Epidemiology

Purpose of Review: Negative controls are a powerful tool to detect and adjust for bias in epidemiological research. This paper introduces negative controls to a broader audience and provides guidance on principled design and causal analysis based on a formal negative control framework. Recent Findings: We review and summarize causal and statistical assumptions, practical strategies, and validation criteria that can be combined with subject matter knowledge to perform negative control analyses. We also review existing statistical methodologies for detection, reduction, and correction of confounding bias, and briefly discuss recent advances towards nonparametric identification of causal effects in a double negative control design. Summary: There is great potential for valid and accurate causal inference leveraging contemporary healthcare data in which negative controls are routinely available. Design and analysis of observational data leveraging negative controls is an area of growing interest in health and social sciences. Despite these developments, further effort is needed to disseminate these novel methods to ensure they are adopted by practicing epidemiologists.

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Identifying effects of multiple treatments in the presence of unmeasured confounding

Identification of treatment effects in the presence of unmeasured confounding is a persistent problem in the social, biological, and medical sciences. The problem of unmeasured confounding in settings with multiple treatments is most common in statistical genetics and bioinformatics settings, where researchers have developed many successful statistical strategies without engaging deeply with the causal aspects of the problem. Recently there have been a number of attempts to bridge the gap between these statistical approaches and causal inference, but these attempts have either been shown to be flawed or have relied on fully parametric assumptions. In this paper, we propose two strategies for identifying and estimating causal effects of multiple treatments in the presence of unmeasured confounding. The auxiliary variables approach leverages variables that are not causally associated with the outcome; in the case of a univariate confounder, our method only requires one auxiliary variable, unlike existing instrumental variable methods that would require as many instruments as there are treatments. An alternative null treatments approach relies on the assumption that at least half of the confounded treatments have no causal effect on the outcome, but does not require a priori knowledge of which treatments are null. Our identification strategies do not impose parametric assumptions on the outcome model and do not rest on estimation of the confounder. This paper extends and generalizes existing work on unmeasured confounding with a single treatment and models commonly used in bioinformatics.

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Identification and estimation of causal effects in the presence of confounded principal strata

The principal stratification has become a popular tool to address a broad class of causal inference questions, particularly in dealing with non-compliance and truncation-by-death problems. The causal effects within principal strata which are determined by joint potential values of the intermediate variable, also known as the principal causal effects, are often of interest in these studies. Analyses of principal causal effects from observed data in the literature mostly rely on ignorability of the treatment assignment, which requires practitioners to accurately measure as many as covariates so that all possible confounding sources are captured. However, collecting all potential confounders in observational studies is often difficult and costly, the ignorability assumption may thus be questionable. In this paper, by leveraging available negative controls that have been increasingly used to deal with uncontrolled confounding, we consider identification and estimation of causal effects when the treatment and principal strata are confounded by unobserved variables. Specifically, we show that the principal causal effects can be nonparametrically identified by invoking a pair of negative controls that are both required not to directly affect the outcome. We then relax this assumption and establish identification of principal causal effects under various semiparametric or parametric models. We also propose an estimation method of principal causal effects. Extensive simulation studies show good performance of the proposed approach and a real data application from the National Longitudinal Survey of Young Men is used for illustration.

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Nonparametric inference about mean functionals of nonignorable nonresponse data without identifying the joint distribution

We consider identification and inference about mean functionals of observed covariates and an outcome variable subject to nonignorable missingness. By leveraging a shadow variable, we establish a necessary and sufficient condition for identification of the mean functional even if the full data distribution is not identified. We further characterize a necessary condition for $\sqrt{n}$-estimability of the mean functional. This condition naturally strengthens the identifying condition, and it requires the existence of a function as a solution to a representer equation that connects the shadow variable to the mean functional. Solutions to the representer equation may not be unique, which presents substantial challenges for nonparametric estimation and standard theories for nonparametric sieve estimators are not applicable here. We construct a consistent estimator for the solution set and then adapt the theory of extremum estimators to find from the estimated set a consistent estimator for an appropriately chosen solution. The estimator is asymptotically normal, locally efficient and attains the semiparametric efficiency bound under certain regularity conditions. We illustrate the proposed approach via simulations and a real data application on home pricing.

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Improving efficiency of inference in clinical trials with external control data

Suppose we are interested in the effect of a treatment in a clinical trial. The efficiency of inference may be limited due to small sample size. However, external control data are often available from historical studies. Motivated by an application to Helicobacter pylori infection, we show how to borrow strength from such data to improve efficiency of inference in the clinical trial. Under an exchangeability assumption about the potential outcome mean, we show that the semiparametric efficiency bound for estimating the average treatment effect can be reduced by incorporating both the clinical trial data and external controls. We then derive a doubly robust and locally efficient estimator. The improvement in efficiency is prominent especially when the external control dataset has a large sample size and small variability. Our method allows for a relaxed overlap assumption, and we illustrate with the case where the clinical trial only contains a treated group. We also develop doubly robust and locally efficient approaches that extrapolate the causal effect in the clinical trial to the external population and the overall population. Our results also offer a meaningful implication for trial design and data collection. We evaluate the finite-sample performance of the proposed estimators via simulation. In the Helicobacter pylori infection application, our approach shows that the combination treatment has potential efficacy advantages over the triple therapy.

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Data Integration in Causal Inference

Integrating data from multiple heterogeneous sources has become increasingly popular to achieve a large sample size and diverse study population. This paper reviews development in causal inference methods that combines multiple datasets collected by potentially different designs from potentially heterogeneous populations. We summarize recent advances on combining randomized clinical trial with external information from observational studies or historical controls, combining samples when no single sample has all relevant variables with application to two-sample Mendelian randomization, distributed data setting under privacy concerns for comparative effectiveness and safety research using real-world data, Bayesian causal inference, and causal discovery methods.

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An Introduction to Proximal Causal Learning

A standard assumption for causal inference from observational data is that one has measured a sufficiently rich set of covariates to ensure that within covariate strata, subjects are exchangeable across observed treatment values. Skepticism about the exchangeability assumption in observational studies is often warranted because it hinges on investigators' ability to accurately measure covariates capturing all potential sources of confounding. Realistically, confounding mechanisms can rarely if ever, be learned with certainty from measured covariates. One can therefore only ever hope that covariate measurements are at best proxies of true underlying confounding mechanisms operating in an observational study, thus invalidating causal claims made on basis of standard exchangeability conditions. Causal learning from proxies is a challenging inverse problem which has to date remained unresolved. In this paper, we introduce a formal potential outcome framework for proximal causal learning, which while explicitly acknowledging covariate measurements as imperfect proxies of confounding mechanisms, offers an opportunity to learn about causal effects in settings where exchangeability on the basis of measured covariates fails. Sufficient conditions for nonparametric identification are given, leading to the proximal g-formula and corresponding proximal g-computation algorithm for estimation. These may be viewed as generalizations of Robins' foundational g-formula and g-computation algorithm, which account explicitly for bias due to unmeasured confounding. Both point treatment and time-varying treatment settings are considered, and an application of proximal g-computation of causal effects is given for illustration.

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