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Yunshu Zhang

Publications and source records attributed to Yunshu Zhang.

11 recordsLinked to original sources

Partial Identification of Causal Effects Using Proxy Variables

Proximal causal inference is a framework for evaluating the causal effects in the presence of unmeasured confounding. For point identification, it leverages a pair of proxy variables to identify a bridge function that matches the dependence of potential outcomes or treatment variables on the hidden factors to corresponding functions of observed proxies. Unique identification requires that proxies are sufficiently relevant for hidden factors, a requirement that has previously been formalized as a completeness condition. However, completeness is not empirically testable, and although a bridge function may be well-defined in a given setting, lack of completeness, sometimes manifested by availability of a single type of proxy, may severely limit prospects for identification of a bridge function and thus a causal effect; therefore, potentially restricting the application of the framework. In this paper, we propose partial identification methods that do not require completeness and obviate the need for identification of a bridge function. We establish that proxies can be leveraged to obtain bounds on the causal effect even if available information does not suffice to identify either a bridge function or a corresponding causal effect of interest. Our bounds are non-smooth functionals of the underlying distribution. For inference, we employ LogSumExp approximations that yield smooth lower and upper bounds, and we derive the efficient influence functions of the resulting bound functionals which enable analytic variance estimation, while bootstrap confidence intervals remain available for regular plug-in implementations. We further establish analogous results in related settings where identification hinges upon hidden mediators for which proxies are available, however such proxies are not sufficiently rich for point identification of a bridge function or a corresponding causal effect of interest.

stat.ME

The Multiplicative Instrumental Variable Model

The instrumental variable (IV) design is a common approach to address hidden confounding bias. For validity, an IV must impact the outcome only through its association with the treatment. In addition, IV identification has required a homogeneity condition such as monotonicity or no unmeasured common effect modifier between the additive effect of the treatment on the outcome, and that of the IV on the treatment. In this work, we introduce the Multiplicative Instrumental Variable Model (MIV), which encodes a condition of no multiplicative interaction between the instrument and an unmeasured confounder in the treatment propensity score model. Thus, the MIV provides a novel formalization of the core IV independence condition interpreted as independent mechanisms of action, by which the instrument and hidden confounders influence treatment uptake, respectively. As we formally establish, MIV provides nonparametric identification of the population average treatment effect on the treated (ATT) via a single-arm version of the classical Wald ratio IV estimand, for which we propose a novel class of estimators that are multiply robust and semiparametric efficient. Finally, we illustrate the methods in extended simulations and an application on the causal impact of a job training program on subsequent earnings.

stat.ME

Estimating optimal interpretable individualized treatment regimes from a classification perspective using adaptive LASSO

Real-world data (RWD) gains growing interests to provide a representative sample of the population for selecting the optimal treatment options. However, existing complex black box methods for estimating individualized treatment rules (ITR) from RWD have problems in interpretability and convergence. Providing an interpretable and sparse ITR can be used to overcome the limitation of existing methods. We developed an algorithm using Adaptive LASSO to predict optimal interpretable linear ITR in the RWD. To encourage sparsity, we obtain an ITR by minimizing the risk function with various types of penalties and different methods of contrast estimation. Simulation studies were conducted to select the best configuration and to compare the novel algorithm with the existing state-of-the-art methods. The proposed algorithm was applied to RWD to predict the optimal interpretable ITR. Simulations show that adaptive LASSO had the highest rates of correctly selected variables and augmented inverse probability weighting with Super Learner performed best for estimating treatment contrast. Our method had a better performance than causal forest and R-learning in terms of the value function and variable selection. The proposed algorithm can strike a balance between the interpretability of estimated ITR (by selecting a small set of important variables) and its value.

stat.ME

Augmented match weighted estimators for average treatment effects

Propensity score matching (PSM) and augmented inverse propensity weighting (AIPW) are widely used in observational studies to estimate causal effects. The two approaches present complementary features. The AIPW estimator is doubly robust and locally efficient but can be unstable when the propensity scores are close to zero or one due to weighting by the inverse of the propensity score. On the other hand, PSM circumvents the instability of propensity score weighting but it hinges on the correctness of the propensity score model and cannot attain the semiparametric efficiency bound. Besides, the fixed number of matches, K, renders PSM nonsmooth and thus invalidates standard nonparametric bootstrap inference. This article presents novel augmented match weighted (AMW) estimators that combine the advantages of matching and weighting estimators. AMW adheres to the form of AIPW for its double robustness and local efficiency but it mitigates the instability due to weighting. We replace inverse propensity weights with matching weights resulting from PSM with unfixed K. Meanwhile, we propose a new cross-validation procedure to select K that minimizes the mean squared error anchored around an unbiased estimator of the causal estimand. Besides, we derive the limiting distribution for the AMW estimators showing that they enjoy the double robustness property and can achieve the semiparametric efficiency bound if both nuisance models are correct. As a byproduct of unfixed K which smooths the AMW estimators, nonparametric bootstrap can be adopted for variance estimation and inference. Furthermore, simulation studies and real data applications support that the AMW estimators are stable with extreme propensity scores and their variances can be obtained by naive bootstrap.

stat.ME

A Multiplicative Instrumental Variable Model for Data Missing Not-at-Random

Instrumental variable (IV) methods offer a valuable approach to account for outcome data missing not-at-random. A valid missing data instrument is a measured factor which (i) predicts the nonresponse process and (ii) is independent of the outcome in the underlying population. For point identification, all existing IV methods for missing data including the celebrated Heckman selection model, a priori restrict the extent of selection bias on the outcome scale, therefore potentially understating uncertainty due to missing data. In this work, we introduce an IV framework which allows the degree of selection bias on the outcome scale to remain completely unrestricted. The new approach instead relies for identification on (iii) a key multiplicative selection model, which posits that the instrument and any hidden common correlate of selection and the outcome, do not interact on the multiplicative scale. Interestingly, we establish that any regular statistical functional of the missing outcome is nonparametrically identified under (i)-(iii) via a single-arm Wald ratio estimand reminiscent of the standard Wald ratio estimand in causal inference. For estimation and inference, we characterize the influence function for any functional defined on a nonparametric model for the observed data, which we leverage to develop semiparametric multiply robust IV estimators. Several extensions of the methods are also considered, including the important practical setting of polytomous and continuous instruments. Simulation studies illustrate the favorable finite sample performance of proposed methods, which we further showcase in an HIV study nested within a household health survey study we conducted in Mochudi, Botswana, in which interviewer characteristics are used as instruments to correct for selection bias due to dependent nonresponse in the HIV component of the survey study.

stat.ME

Inference on Nonlinear Counterfactual Functionals under a Multiplicative IV Model

Instrumental variable (IV) methods play a central role in causal inference, particularly in settings where treatment assignment is confounded by unobserved variables. IV methods have been extensively developed in recent years and applied across diverse domains, from economics to epidemiology. In this work, we study the recently introduced multiplicative IV (MIV) model and demonstrate its utility for causal inference beyond the average treatment effect. In particular, we show that it enables identification and inference for a broad class of counterfactual functionals characterized by moment equations. This includes, for example, inference on quantile treatment effects. We develop methods for efficient and multiply robust estimation of such functionals, and provide inference procedures with asymptotic validity. Experimental results demonstrate that the proposed procedure performs well even with moderate sample sizes.

stat.ME

Dissecting RGB-D Learning for Improved Multi-modal Fusion

In the RGB-D vision community, extensive research has been focused on designing multi-modal learning strategies and fusion structures. However, the complementary and fusion mechanisms in RGB-D models remain a black box. In this paper, we present an analytical framework and a novel score to dissect the RGB-D vision community. Our approach involves measuring proposed semantic variance and feature similarity across modalities and levels, conducting visual and quantitative analyzes on multi-modal learning through comprehensive experiments. Specifically, we investigate the consistency and specialty of features across modalities, evolution rules within each modality, and the collaboration logic used when optimizing a RGB-D model. Our studies reveal/verify several important findings, such as the discrepancy in cross-modal features and the hybrid multi-modal cooperation rule, which highlights consistency and specialty simultaneously for complementary inference. We also showcase the versatility of the proposed RGB-D dissection method and introduce a straightforward fusion strategy based on our findings, which delivers significant enhancements across various tasks and even other multi-modal data.

cs.CV

Transfer Learning for Individualized Treatment Rules: Application to Sepsis Patients Data from eICU-CRD and MIMIC-III Databases

Modern precision medicine aims to utilize real-world data to provide the best treatment for an individual patient. An individualized treatment rule (ITR) maps each patient's characteristics to a recommended treatment scheme that maximizes the expected outcome of the patient. A challenge precision medicine faces is population heterogeneity, as studies on treatment effects are often conducted on source populations that differ from the populations of interest in terms of the distribution of patient characteristics. Our research goal is to explore a transfer learning algorithm that aims to address the population heterogeneity problem and obtain targeted, optimal, and interpretable ITRs. The algorithm incorporates a calibrated augmented inverse probability weighting (CAIPW) estimator for the average treatment effect (ATE) and employs value function maximization for the target population using Genetic Algorithm (GA) to produce our desired ITR. To demonstrate its practical utility, we apply this transfer learning algorithm to two large medical databases, Electronic Intensive Care Unit Collaborative Research Database (eICU-CRD) and Medical Information Mart for Intensive Care III (MIMIC-III). We first identify the important covariates, treatment options, and outcomes of interest based on the two databases, and then estimate the optimal linear ITRs for patients with sepsis. Our research introduces and applies new techniques for data fusion to obtain data-driven ITRs that cater to patients' individual medical needs in a population of interest. By emphasizing generalizability and personalized decision-making, this methodology extends its potential application beyond medicine to fields such as marketing, technology, social sciences, and education.

stat.AP

Multiply robust matching estimators of average and quantile treatment effects

Propensity score matching has been a long-standing tradition for handling confounding in causal inference, however requiring stringent model assumptions. In this article, we propose double score matching(DSM) for general causal estimands utilizing two balancing scores including the propensity score and prognostic score. To gain the protection of possible model misspecification, we posit multiple candidate models for each score. We show that the de-biasing DSM estimator achieves the multiple robustness property in that it is consistent for the true causal estimand if any model of the propensity score or prognostic score is correct.

stat.ME

High dimensional precision medicine from patient-derived xenografts

The complexity of human cancer often results in significant heterogeneity in response to treatment. Precision medicine offers potential to improve patient outcomes by leveraging this heterogeneity. Individualized treatment rules (ITRs) formalize precision medicine as maps from the patient covariate space into the space of allowable treatments. The optimal ITR is that which maximizes the mean of a clinical outcome in a population of interest. Patient-derived xenograft (PDX) studies permit the evaluation of multiple treatments within a single tumor and thus are ideally suited for estimating optimal ITRs. PDX data are characterized by correlated outcomes, a high-dimensional feature space, and a large number of treatments. Existing methods for estimating optimal ITRs do not take advantage of the unique structure of PDX data or handle the associated challenges well. In this paper, we explore machine learning methods for estimating optimal ITRs from PDX data. We analyze data from a large PDX study to identify biomarkers that are informative for developing personalized treatment recommendations in multiple cancers. We estimate optimal ITRs using regression-based approaches such as Q-learning and direct search methods such as outcome weighted learning. Finally, we implement a superlearner approach to combine a set of estimated ITRs and show that the resulting ITR performs better than any of the input ITRs, mitigating uncertainty regarding user choice of any particular ITR estimation methodology. Our results indicate that PDX data are a valuable resource for developing individualized treatment strategies in oncology.

stat.ML

Sharp bounds on the relative treatment effect for ordinal outcomes

For ordinal outcomes, the average treatment effect is often ill-defined and hard to interpret. Echoing Agresti and Kateri (2017), we argue that the relative treatment effect can be a useful measure especially for ordinal outcomes, which is defined as $γ= \mathrm{pr}\{ Y_i(1) > Y_i(0) \} - \mathrm{pr}\{ Y_i(1) < Y_i(0) \}$, with $Y_i(1)$ and $Y_i(0)$ being the potential outcomes of unit $i$ under treatment and control, respectively. Given the marginal distributions of the potential outcomes, we derive the sharp bounds on $γ,$ which are identifiable parameters based on the observed data. Agresti and Kateri (2017) focused on modeling strategies under the assumption of independent potential outcomes, but we allow for arbitrary dependence.

stat.ME