Predicting risks of chronic diseases has become increasingly important in clinical practice. When a prediction model is developed in a given source cohort, there is often a great interest to apply the model to other cohorts. However, due to potential discrepancy in baseline disease incidences between different cohorts and shifts in patient composition, the risk predicted by the original model often under- or over-estimates the risk in the new cohort. The remedy of such a poorly calibrated prediction is needed for proper medical decision-making. In this article, we assume the relative risks of predictors are the same between the two cohorts, and propose a novel weighted estimating equation approach to re-calibrating the projected risk for the targeted population through updating the baseline risk. The recalibration leverages the knowledge about the overall survival probabilities for the disease of interest and competing events, and the summary information of risk factors from the targeted population. The proposed re-calibrated risk estimators gain efficiency if the risk factor distributions are the same for both the source and target cohorts, and are robust with little bias if they differ. We establish the consistency and asymptotic normality of the proposed estimators. Extensive simulation studies demonstrate that the proposed estimators perform very well in terms of robustness and efficiency in finite samples. A real data application to colorectal cancer risk prediction also illustrates that the proposed method can be used in practice for model recalibration.
Many clinical endpoint measures, such as the number of standard drinks consumed per week or the number of days that patients stayed in the hospital, are count data with excessive zeros. However, the zero-inflated nature of such outcomes is sometimes ignored in analyses of clinical trials. This leads to biased estimates of study-level intervention effect and, consequently, a biased estimate of the overall intervention effect in a meta-analysis. The current study proposes a novel statistical approach, the Zero-inflation Bias Correction (ZIBC) method, that can account for the bias introduced when…
Hazard ratios are often used to evaluate time to event outcomes, but they may be hard to interpret. A particular issue arise because hazards are typically estimated conditional on survival, i.e.\ on left truncated samples. Then, hazard ratios from conventional models cannot be interpreted as counterfactual hazard ratios that are immediately relevant to individual patients. This article explores how the hazard ratios from Cox models may differ from hazard ratios with a causal interpretation. Using summary data from twin studies, I suggest an approach to learn about the unmeasured heterogeneity …
Individualizing treatment assignment can improve outcomes for diseases with patient-to-patient variability in comparative treatment effects. When a clinical trial demonstrates that some patients improve on treatment while others do not, it is tempting to assume that treatment effect heterogeneity exists. However, if variability in response is mainly driven by factors other than treatment, investigating the extent to which covariate data can predict differential treatment response is a potential waste of resources. Motivated by recent meta-analyses assessing the potential of individualizing tre…
Mendelian randomization (MR) is a powerful method that uses genetic variants as instrumental variables (IVs) to infer the causal effect of a modifiable exposure on an outcome. Although recent years have seen many extensions of basic MR methods to be robust to certain violations of assumptions, few methods were proposed to infer bi-directional causal relationships, especially for phenotypes with limited biological understandings. The presence of horizontal pleiotropy adds another layer of complexity. In this article, we show that assumptions for common MR methods are often impossible or too str…
Mendelian randomization (MR) has been a popular method in genetic epidemiology to estimate the effect of an exposure on an outcome using genetic variants as instrumental variables (IV), with two-sample summary-data MR being the most popular. Unfortunately, instruments in MR studies are often weakly associated with the exposure, which can bias effect estimates and inflate Type I errors. In this work, we propose test statistics that are robust under weak instrument asymptotics by extending the Anderson-Rubin, Kleibergen, and the conditional likelihood ratio test in econometrics to two-sample sum…
Approximate Bayesian computation (ABC) and other likelihood-free inference methods have gained popularity in the last decade, as they allow rigorous statistical inference for complex models without analytically tractable likelihood functions. A key component for accurate inference with ABC is the choice of summary statistics, which summarize the information in the data, but at the same time should be low-dimensional for efficiency. Several dimension reduction techniques have been introduced to automatically construct informative and low-dimensional summaries from a possibly large pool of candi…
Mass spectrometry based clinical proteomics has emerged as a powerful tool for highthroughput protein profiling and biomarker discovery. Recent improvements in mass spectrometry technology have boosted the potential of proteomic studies in biomedical research. However, the complexity of the proteomic expression introduces new statistical challenges in summarizing and analyzing the acquired data. Statistical methods for optimally processing proteomic data are currently a growing field of research. In this paper we present simple, yet appropriate methods to preprocess, summarize and analyze high…
Current estimation methods for the probability of causation (PC) make strong parametric assumptions or are inefficient. We derive a nonparametric influence-function-based estimator for a projection of PC, which allows for simple interpretation and valid inference by making weak structural assumptions. We apply our estimator to real data from an experiment in Kenya, which found, by estimating the average treatment effect, that protecting water springs reduces childhood disease. However, before scaling up this intervention, it is important to determine whether it was the exposure, and not someth…
The results from Genome-Wide Association Studies (GWAS) on thousands of phenotypes provide an unprecedented opportunity to infer the causal effect of one phenotype (exposure) on another (outcome). Mendelian randomization (MR), an instrumental variable (IV) method, has been introduced for causal inference using GWAS data. Due to the polygenic architecture of complex traits/diseases and the ubiquity of pleiotropy, however, MR has many unique challenges compared to conventional IV methods. We propose a Bayesian weighted Mendelian randomization (BWMR) for causal inference to address these challeng…
When data on treatment assignment, outcomes, and covariates from a randomized trial are available, a question of interest is to what extent covariates can be used to optimize treatment decisions. Statistical hypothesis testing of covariate-by-treatment interaction is ill-suited for this purpose. The application of decision theory results in treatment rules that compare the expected benefit of treatment given the patient's covariates against a treatment threshold. However, determining treatment threshold is often context-specific, and any given threshold might seem arbitrary when the overall ca…
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…
Mendelian randomization (MR) has become a popular approach to study the effect of a modifiable exposure on an outcome by using genetic variants as instrumental variables. A challenge in MR is that each genetic variant explains a relatively small proportion of variance in the exposure and there are many such variants, a setting known as many weak instruments. To this end, we provide a theoretical characterization of the statistical properties of two popular estimators in MR, the inverse-variance weighted (IVW) estimator and the IVW estimator with screened instruments using an independent select…
Causally Interpretable Meta-Mediation Analysis With Missing At Random Mediator and Outcome Data
EPILOGY, Institut Mondor of Biomedical Research, INSERM U955（INSERM U955 蒙多尔生物医学研究所 EPILOGY）；Université Paris-Est Créteil（巴黎东克雷泰伊大学）；Mines Paris, Université Paris Sciences Lettres（巴黎矿业学院，巴黎文理研究大学）；Department of Mathematics, Université du Québec à Montréal（蒙特利尔大学数学系）
In classical study designs, the aim is often to learn about the effects of a treatment or intervention on a single outcome; in many modern studies, however, data on multiple outcomes are collected and it is of interest to explore effects on multiple outcomes simultaneously. Such designs can be particularly useful in patient-centered research, where different outcomes might be more or less important to different patients. In this paper we propose scaled effect measures (via potential outcome notation) that translate effects on multiple outcomes to a common scale, using mean-variance and median-…
Learning conditional densities and identifying factors that influence the entire distribution are vital tasks in data-driven applications. Conventional approaches work mostly with summary statistics, and are hence inadequate for a comprehensive investigation. Recently, there have been developments on functional regression methods to model density curves as functional outcomes. A major challenge for developing such models lies in the inherent constraint of non-negativity and unit integral for the functional space of density outcomes. To overcome this fundamental issue, we propose Wasserstein Di…
Researchers increasingly use meta-analysis to synthesize the results of several studies in order to estimate a common effect. When the outcome variable is continuous, standard meta-analytic approaches assume that the primary studies report the sample mean and standard deviation of the outcome. However, when the outcome is skewed, authors sometimes summarize the data by reporting the sample median and one or both of (i) the minimum and maximum values and (ii) the first and third quartiles, but do not report the mean or standard deviation. To include these studies in meta-analysis, several metho…
Approximate Bayesian computation (ABC) methods make use of comparisons between simulated and observed summary statistics to overcome the problem of computationally intractable likelihood functions. As the practical implementation of ABC requires computations based on vectors of summary statistics, rather than full data sets, a central question is how to derive low-dimensional summary statistics from the observed data with minimal loss of information. In this article we provide a comprehensive review and comparison of the performance of the principal methods of dimension reduction proposed in t…
Historically used in settings where the outcome is rare or data collection is expensive, outcome-dependent sampling is relevant to many modern settings where data is readily available for a biased sample of the target population, such as public administrative data. Under outcome-dependent sampling, common effect measures such as the average risk difference and the average risk ratio are not identified, but the conditional odds ratio is. Aggregation of the conditional odds ratio is challenging since summary measures are generally not identified. Furthermore, the marginal odds ratio can be large…
There is growing interest in producing estimates of demographic and global health indicators in populations with limited data. Statistical models are needed to combine data from multiple data sources into estimates and projections with uncertainty. Diverse modeling approaches have been applied to this problem, making comparisons between models difficult. We propose a model class, Temporal Models for Multiple Populations (TMMPs), to facilitate documentation of model assumptions in a standardized way and comparison across models. The class distinguishes between latent trends and the observed dat…
A Plasmode Benchmark Can Refute but Cannot Certify: Projection and Regularity in Causal-Inference Simulation
School of Population and Public Health, University of British Columbia（不列颠哥伦比亚大学公共卫生与人口健康学院）；Centre for Advancing Health Outcomes, St. Paul’s Hospital（圣保罗医院健康成果促进中心）
