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Federated causal inference in heterogeneous observational data.基于异质观测数据的联邦因果推断。
Stat Med. 2023 Oct 30;42(24):4418-4439. doi: 10.1002/sim.9868. Epub 2023 Aug 8.
3
Batch effects removal for microbiome data via conditional quantile regression.通过条件分位数回归去除微生物组数据的批次效应。
Nat Commun. 2022 Sep 15;13(1):5418. doi: 10.1038/s41467-022-33071-9.
4
A calibration approach to transportability and data-fusion with observational data.一种将观测数据进行可传输性和数据融合的校准方法。
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Effectiveness of Covid-19 Vaccines over a 9-Month Period in North Carolina.北卡罗来纳州 9 个月期间的新冠疫苗有效性。
N Engl J Med. 2022 Mar 10;386(10):933-941. doi: 10.1056/NEJMoa2117128. Epub 2022 Jan 12.
6
Comparative Effectiveness of BNT162b2 and mRNA-1273 Vaccines in U.S. Veterans.BNT162b2 与 mRNA-1273 疫苗在美国退伍军人中的比较效力。
N Engl J Med. 2022 Jan 13;386(2):105-115. doi: 10.1056/NEJMoa2115463. Epub 2021 Dec 1.
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Improving trial generalizability using observational studies.利用观察性研究提高试验的概括性。
Biometrics. 2023 Jun;79(2):1213-1225. doi: 10.1111/biom.13609. Epub 2022 Jan 11.
8
International electronic health record-derived COVID-19 clinical course profiles: the 4CE consortium.国际电子健康记录衍生的COVID-19临床病程概况:4CE联盟
NPJ Digit Med. 2020 Aug 19;3:109. doi: 10.1038/s41746-020-00308-0. eCollection 2020.
9
Extending inferences from a randomized trial to a new target population.将随机试验的推断扩展到新的目标人群。
Stat Med. 2020 Jun 30;39(14):1999-2014. doi: 10.1002/sim.8426. Epub 2020 Apr 6.
10
A fast score test for generalized mixture models.广义混合模型的快速得分检验。
Biometrics. 2020 Sep;76(3):811-820. doi: 10.1111/biom.13204. Epub 2019 Dec 31.

目标治疗效果的联合自适应因果估计(FACE)

Federated Adaptive Causal Estimation (FACE) of Target Treatment Effects.

作者信息

Han Larry, Hou Jue, Cho Kelly, Duan Rui, Cai Tianxi

机构信息

Department of Biostatistics, Harvard University.

Department of Public Health and Health Sciences, Northeastern University.

出版信息

J Am Stat Assoc. 2025 Mar 17. doi: 10.1080/01621459.2025.2453249.

DOI:10.1080/01621459.2025.2453249
PMID:40895281
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12396575/
Abstract

Federated learning of causal estimands may greatly improve estimation efficiency by leveraging data from multiple study sites, but robustness to heterogeneity and model misspecifications is vital for ensuring validity. We develop a Federated Adaptive Causal Estimation (FACE) framework to incorporate heterogeneous data from multiple sites to provide treatment effect estimation and inference for a flexibly specified target population of interest. FACE accounts for site-level heterogeneity in the distribution of covariates through density ratio weighting. To safely incorporate source sites and avoid negative transfer, we introduce an adaptive weighting procedure via a penalized regression, which achieves both consistency and optimal efficiency. Our strategy is communication-efficient and privacy-preserving, allowing participating sites to share summary statistics only once with other sites. We conduct both theoretical and numerical evaluations of FACE and apply it to conduct a comparative effectiveness study of BNT162b2 (Pfizer) and mRNA-1273 (Moderna) vaccines on COVID-19 outcomes in U.S. veterans using electronic health records from five VA regional sites. We show that compared to traditional methods, FACE meaningfully increases the precision of treatment effect estimates, with reductions in standard errors ranging from 26% to 67%.

摘要

因果估计量的联邦学习可以通过利用来自多个研究地点的数据极大地提高估计效率,但对异质性和模型错误设定的稳健性对于确保有效性至关重要。我们开发了一个联邦自适应因果估计(FACE)框架,以整合来自多个地点的异质数据,为灵活指定的目标感兴趣人群提供治疗效果估计和推断。FACE通过密度比加权来考虑协变量分布中的地点级异质性。为了安全地纳入源地点并避免负迁移,我们通过惩罚回归引入了一种自适应加权程序,该程序实现了一致性和最优效率。我们的策略具有通信效率且能保护隐私,允许参与的地点仅与其他地点共享一次汇总统计信息。我们对FACE进行了理论和数值评估,并将其应用于使用来自五个退伍军人事务部(VA)地区地点的电子健康记录,对BNT162b2(辉瑞)和mRNA-1273(莫德纳)疫苗在美国退伍军人中对COVID-19结局的比较有效性研究。我们表明,与传统方法相比,FACE显著提高了治疗效果估计的精度,标准误差降低了26%至67%。