Evidence mapPaperPMID 42425926Full record

ArticleBiostatistics (Oxford, England)2026

Data-adaptive identification of effect modifiers through stochastic shift interventions and cross-validated targeted learning.

David McCoy, Wenxin Zhang, Alan Hubbard, Mark van der Laan, Alejandro Schuler

Abstract read
In one paragraph

Article in Biostatistics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

David McCoyDivision of Biostatistics, University of California, Berkeley, 2121 Berkeley Way, Berkeley, CA 94720, United States.ORCID 0000-0002-5515-6307
Wenxin ZhangDivision of Biostatistics, University of California, Berkeley, 2121 Berkeley Way, Berkeley, CA 94720, United States.
Alan HubbardDivision of Biostatistics, University of California, Berkeley, 2121 Berkeley Way, Berkeley, CA 94720, United States.
Mark van der LaanDivision of Biostatistics, University of California, Berkeley, 2121 Berkeley Way, Berkeley, CA 94720, United States.
Alejandro SchulerDivision of Biostatistics, University of California, Berkeley, 2121 Berkeley Way, Berkeley, CA 94720, United States.

Funding

TOXIC SUBSTANCES IN THE ENVIRONMENTP42ES004705 · UNIVERSITY OF CALIFORNIA BERKELEY · 1987 to 2025
$25.9M
California Office of Environmental Health Hazard Assessment unde 22-E0010NIEHS NIH HHS P42 ES004705NIH HHS P42ES004705
6 · The paper itself

Abstract

In epidemiology, identifying subpopulations that are particularly vulnerable to exposures and those who may benefit differently from exposure-reducing interventions is essential. Factors such as age, gender-specific vulnerabilities, and physiological states such as pregnancy are critical for policymakers when setting regulatory guidelines. However, current semiparametric methods for estimating heterogeneous treatment effects are often limited to binary exposures and can function as black boxes, lacking clear, interpretable rules for subpopulation-specific policy interventions. This study introduces a novel method that uses cross-validated targeted minimum loss-based estimation (TMLE) paired with a data-adaptive target parameter strategy to identify subpopulations with the most significant differential impact of simulated policy interventions that reduce exposure. Our approach is assumption-lean, allowing for the integration of machine learning while still yielding valid confidence intervals. We demonstrate the robustness of our methodology through simulations and an application to data from the National Health and Nutrition Examination Survey. Our analysis of NHANES data on persistent organic pollutants (POPs) and leukocyte telomere length (LTL) identified age as a significant effect modifier. Specifically, we found that exposure to 3,3',4,4',5-pentachlorobiphenyl (PCB; NHANES analyte LBXPCBLA) consistently had a differential impact on LTL, with a 1-SD reduction in exposure leading to a more pronounced increase in LTL among younger populations than in older ones. We offer our method as an open-source software package, EffectXshift, enabling researchers to investigate the effect modification of continuous exposures. The EffectXshift package provides clear and interpretable results, informing targeted public health interventions and policydecisions.

Indexed as

BiostatisticsEnvironmental ExposureMachine LearningModels, StatisticalData Interpretation, StatisticalHumansNutrition SurveysStochastic ProcessesTreatment Effect Heterogeneitycausal inferenceeffect modificationenvironmental exposuresstochastic interventionstargeted maximum likelihood estimation

Identifiers

PMID42425926
PMCPMC13349617

What Socratic holds

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LicenceCC BY-NC
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.