Evidence map›Paper›PMID 41329193›Full record

ArticleBiometrics2025

Flexible and efficient estimation of causal effects with error-prone exposures: a control variates approach for measurement error.

Keith Barnatchez, Rachel Nethery, Bryan E Shepherd, Giovanni Parmigiani, Kevin P Josey

Abstract read
In one paragraph

Article in Biometrics, 2025. 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.

Keith BarnatchezDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA 02115, United States.ORCID 0000-0002-1451-9335
Rachel NetheryDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA 02115, United States.ORCID 0000-0001-9895-1477
Bryan E ShepherdDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, TN 37232, United States.
Giovanni ParmigianiDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA 02115, United States.ORCID 0000-0002-8783-5961
Kevin P JoseyDepartment of Biostatistics and Informatics, Colorado School of Public Health, Aurora, CO 80045, United States.ORCID 0000-0003-2490-6272

Funding

Tennessee CFAR: Implementation of Culturally Responsive Trauma-Informed Care with Youth with HIV in Memphis, TNP30AI110527 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI John Koethe · 2015 to 2026
$27.5M
BIOSTATISTICS/EPIDEMIOLOGY TRAINING GRANTS IN AIDST32AI007358 · NIAID · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI Michael David Hughes · 1989 to 2026
$12.4M
Statistical methods and designs for correlated outcome and covariate errors in studies of HIV/AIDSR37AI131771 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Pamela A Shaw, Bryan Earl Shepherd · 2023 to 2026
$3.4M
Causal machine learning methods for studying the effects of environmental exposures on childhood cancer using natural experimentsK01ES032458 · NIEHS · HARVARD SCHOOL OF PUBLIC HEALTH · PI NETHERY, RACHEL C · 2021 to 2023
$417k
National Institute of Health K01ES032458National Institute of Health P30AI110527National Institute of Health R37AI131771National Institute of Health T32AI007358NIAID NIH HHS P30 AI110527NIAID NIH HHS R37 AI131771NIAID NIH HHS T32 AI007358NIEHS NIH HHS K01 ES032458
6 · The paper itself

Abstract

Exposure measurement error is a ubiquitous but often overlooked challenge in causal inference with observational data. Existing methods accounting for exposure measurement error largely rely on restrictive parametric assumptions, while emerging data-adaptive estimation approaches allow for less restrictive assumptions but at the cost of flexibility, as they are typically tailored toward rigidly defined statistical quantities. There remains a critical need for assumption-lean estimation methods that are both flexible and possess desirable theoretical properties across a variety of study designs. In this paper, we introduce a general framework for estimation of causal quantities in the presence of exposure measurement error, adapted from the method of control variates. Our method can be implemented in various two-phase sampling study designs, where one obtains gold-standard exposure measurements for a small subset of the full study sample, called the validation data. The control variates framework leverages both the error-prone and error-free exposure measurements by augmenting an initial consistent estimator from the validation data with a variance reduction term formed from the full data. We show that our method inherits double-robustness properties under standard causal assumptions. Simulation studies show that our approach performs favorably compared to leading methods under various two-phase sampling schemes. We illustrate our method with observational electronic health record data on HIV outcomes from the Vanderbilt Comprehensive Care Clinic.

Indexed as

BiometryCausalityModels, StatisticalBiasComputer SimulationData Interpretation, StatisticalHIV InfectionsHumanscausal inferencecontrol variatesdoubly robustHIVmeasurement errorvalidation data

Identifiers

PMID41329193
PMCPMC12882774

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Registered trials

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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 OpenQuestion graph.