Causal Inference of Blood Pressure Reduction and Coronary Heart Disease Risk in the Framingham Study
弗雷明汉研究中降血压与冠心病风险的因果推断AI 解读 ↓
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弗雷明汉研究中降血压与冠心病风险的因果推断AI 解读 ↓
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Standard cardiovascular risk calculators, including the Framingham Risk Score and the ACC/AHA Pooled Cohort Equations, estimate the conditional probability P(CHD | SysBP = s) rather than the interventional quantity P(CHD | do(SysBP = s)). When confounding is present, this distinction has direct clinical consequences: observational estimates may systematically overstate the absolute benefit of antihypertensive treatment. We applied Pearl's do-calculus to the Framingham Heart Study Offspring Cohort (n = 4,240; primary analysis on 3,776 complete cases; 574 ten-year coronary heart disease events). A structurally corrected directed acyclic graph (DAG) was specified and evaluated using conditional independence testing. The average causal effect (ACE) of a 20 mmHg systolic blood pressure reduction was estimated by g-computation with bootstrap confidence intervals, corroborated by propensity score matching and inverse probability weighting. G-computation yielded an ACE of 3.40 percent absolute risk reduction (95 percent CI: 2.64 to 4.14), compared with a naive observational estimate of 4.14 percent, corresponding to an approximate 21.8 percent relative overestimation. Conditional average treatment effects were estimated using R-Learner and T-Learner metalearners. These findings suggest that observational cardiovascular risk tools may overestimate the absolute benefit of blood pressure reduction, with implications for clinical risk stratification and prescribing thresholds.
Motivation: Mediation analysis is an important tool for elucidating causal mechanisms in biomedical research and has recently gained increasing attention in microbiome studies. Motivated by a microbiome study of acute myeloid leukemia (AML) patients, we investigate whether the effect of induction chemotherapy intensity on infection status is mediated through gut microbial taxa. This problem poses substantial methodological challenges due to the high dimensionality, zero…
I study randomization inference for dynamic causal effects in panels with many units and few periods when treatment is endogenous and an instrument is as good as randomly assigned only through the innovations of a first-order autoregressive assignment mechanism with unknown persistence. The persistence is a nuisance parameter in two senses: it determines which weighted average of heterogeneous causal effects the instrumented local projection estimand measures, and it governs…
Two frequent approaches for identifying structural VARs are external instruments, which carry economic content but are often weak, and non-Gaussianity of the shocks, which provides statistical identification but carries no economic meaning. We combine the two strategies in a single generalized method of moments framework. This hybrid approach point-identifies the target shocks while also identifying the non-target shocks up to sign and ordering. Under suitable rank…
克隆—删失—加权方法的形式化与一致性
Target trial emulation has become a standard framework for causal inference from observational data. Within this paradigm, the clone-censor-weight (CCW) methodology provides a practical way to deal with complex treatment and adherence definitions when treatment regimes are not distinguishable at baseline. Despite its increasing use, the statistical interpretation of CCW remains limited. In this work, we formalize the CCW methodology from a statistical viewpoint based on…
非精确匹配何时能在无需调整的情况下保证平衡与有效推断?
One-to-one matching without replacement is a classical approach to constructing comparable treated and control samples in the design of observational studies. It pairs each treated unit with a distinct control while minimizing a covariate distance objective. With continuous covariates, the matched pairs generally remain inexact, which contributes to bias in downstream analysis. Its key theoretical properties, such as the resulting imbalance between matched pairs and when it…
We study nonparametric inference for a continuous-treatment causal dose-response curve and its first derivative under unmeasured confounding, using treatment- and outcome-inducing proxies. We establish a proximal doubly robust pseudo-outcome whose conditional mean given treatment equals the dose-response curve whenever either bridge function is correctly specified. Their (smoothed) efficient influence function representations lead to cross-fitted local-polynomial estimators…