Evidence map›Paper›PMID 24151138›Full record

ArticleStatistics in medicine2014

Simulation from a known Cox MSM using standard parametric models for the g-formula.

Jessica G Young, Eric J Tchetgen Tchetgen

Abstract read
In one paragraph

Article in Statistics in medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

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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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Simulating Data From Marginal Structural Models for a Survival Time Outcome.Biometrical journal. Biometrische Zeitschrift · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Article
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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

2 authors.

Jessica G YoungDepartment of Epidemiology, Harvard School of Public Health, Boston, MA 02115.
Eric J Tchetgen Tchetgen

Funding

Estimating Effects of Interventions in Longitudinal DataR01HL080644 · NHLBI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI HERNAN, MIGUEL · 2005 to 2013
$4.0M
Identification and Inference for Longitudinal Causal Mediation Analysis in HIVR01AI104459 · NIAID · HARVARD SCHOOL OF PUBLIC HEALTH · PI SHPITSER, ILYA, VANDERWEELE, TYLER · 2013 to 2017
$2.0M
Semiparametric Methods for Gene-environment InteractionR01ES020337 · NIEHS · HARVARD SCHOOL OF PUBLIC HEALTH · PI TCHETGEN TCHETGEN, ERIC JOEL · 2012 to 2015
$1.4M
Semiparametric Methods for Secondary Outcomes in Case-control StudiesR21ES019712 · NIEHS · HARVARD SCHOOL OF PUBLIC HEALTH · PI TCHETGEN TCHETGEN, ERIC JOEL · 2011 to 2012
$472k
NHLBI NIH HHS HL080644NHLBI NIH HHS R01 HL080644NIAID NIH HHS R01 AI104459NIAID NIH HHS R01AI104459-01A1NIEHS NIH HHS 1R21ES019712-01NIEHS NIH HHS R01 ES020337NIEHS NIH HHS R21 ES019712
6 · The paper itself

Abstract

It is routinely argued that, unlike standard regression-based estimates, inverse probability weighted (IPW) estimates of the parameters of a correctly specified Cox marginal structural model (MSM) may remain unbiased in the presence of a time-varying confounder affected by prior treatment. Previously proposed methods for simulating from a known Cox MSM lack knowledge of the law of the observed outcome conditional on the measured past. Although unbiased IPW estimation does not require this knowledge, standard regression-based estimates rely on correct specification of this law. Thus, in typical high-dimensional settings, such simulation methods cannot isolate bias due to complex time-varying confounding as it may be conflated with bias due to misspecification of the outcome regression model. In this paper, we describe an approach to Cox MSM data generation that allows for a comparison of the bias of IPW estimates versus that of standard regression-based estimates in the complete absence of model misspecification. This approach involves simulating data from a standard parametrization of the likelihood and solving for the underlying Cox MSM. We prove that solutions exist and computations are tractable under many data-generating mechanisms. We show analytically and confirm in simulations that, in the absence of model misspecification, the bias of standard regression-based estimates for the parameters of a Cox MSM is indeed a function of the coefficients in observed data models quantifying the presence of a time-varying confounder affected by prior treatment. We discuss limitations of this approach including that implied by the 'g-null paradox'.

Indexed as

Models, StatisticalProportional Hazards ModelsAlgorithmsAnalysis of VarianceBiasBiostatisticsCausalityComputer SimulationHumansMarkov ChainsRegression Analysiscausal inferenceg-formulag-null paradoxmarginal structural modelssimulationsurvival analysis

Identifiers

PMID24151138
PMCPMC3947915

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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.