Variable Selection for the Propensity Score Model: Beyond Main Effects and Linear Relations

Propensity score methods are frequently used to estimate treatment effects in observational studies. The propensity score is usually estimated using a logistic regression model with additive and linear effects. The limited literature on variable selection for the propensity score model is consistent in its suggestion that the propensity score model should include those variables that are prognostically important for the study outcome. However, the existing literature has focused only on main effects and assumed linear relations between continuous variables and outcomes. We used Monte Carlo simulations to study the impact of omitting quadratic terms and interaction terms from the propensity score model when these terms were prognostically important. We compared two formulations of the propensity score model: a simple formulation that included only main effects and omitted all interactions and quadratic terms and a complex formulation that included main effects in addition to prognostically important interactions and quadratic terms. We examined 168 scenarios defined by the nature of the true treatment-selection model, the nature of the true outcome regression model, and by sample size. In 95% of scenarios, bias in estimated risk differences, along with coverage rates of estimated 95% confidence intervals, did not differ between the two specifications of the propensity score model when using inverse probability of treatment weighting. In only 5% of scenarios was bias substantially higher and coverage rates substantially lower when using the simple specification of the propensity score model compared to when using the complex specification of the propensity score model.

Authors

Institutions

Publication Details

Journal
Pharmaceutical Statistics
Published
2026-10-16
DOI
https://doi.org/10.1002/pst.70135
Primary Topic
Advanced Causal Inference Techniques
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Variable Selection for the Propensity Score Model: Beyond Main Effects and Linear Relations

Peter C. Austin, Guy Cafri
Pharmaceutical Statistics
Advanced Causal Inference Techniques
article

Variable Selection for the Propensity Score Model: Beyond Main Effects and Linear Relations

Peter C. Austin, Guy Cafri
article en

Abstract

Propensity score methods are frequently used to estimate treatment effects in observational studies. The propensity score is usually estimated using a logistic regression model with additive and linear effects. The limited literature on variable selection for the propensity score model is consistent in its suggestion that the propensity score model should include those variables that are prognostically important for the study outcome. However, the existing literature has focused only on main effects and assumed linear relations between continuous variables and outcomes. We used Monte Carlo simulations to study the impact of omitting quadratic terms and interaction terms from the propensity score model when these terms were prognostically important. We compared two formulations of the propensity score model: a simple formulation that included only main effects and omitted all interactions and quadratic terms and a complex formulation that included main effects in addition to prognostically important interactions and quadratic terms. We examined 168 scenarios defined by the nature of the true treatment-selection model, the nature of the true outcome regression model, and by sample size. In 95% of scenarios, bias in estimated risk differences, along with coverage rates of estimated 95% confidence intervals, did not differ between the two specifications of the propensity score model when using inverse probability of treatment weighting. In only 5% of scenarios was bias substantially higher and coverage rates substantially lower when using the simple specification of the propensity score model compared to when using the complex specification of the propensity score model.

Pharmaceutical StatisticsVol. 25(6)
Johnson & Johnson (United States) (US), University of Toronto (CA), Institute for Clinical Evaluative Sciences (CA), Sunnybrook Hospital (CA), Sunnybrook Research Institute
Openalex Percentile: Top 12%
Advanced Causal Inference Techniques
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.