Evidence map›Paper›PMID 42665560›Full record

ArticlePharmaceutical statistics

Robustness of the Pairwise-Fitting Approach Under Missing at Random Dropout: A Case and Simulation Study.

Dries De Witte, Geert Verbeke, Thomas Neyens, Ariel Alonso Abad, Geert Molenberghs

Abstract read
In one paragraph

Article in Pharmaceutical statistics. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Dries De WitteL-BioStat, KU Leuven, Leuven, Belgium.ORCID https://orcid.org/0000-0003-3264-6984
Geert VerbekeL-BioStat, KU Leuven, Leuven, Belgium.ORCID https://orcid.org/0000-0001-8430-7576
Thomas NeyensL-BioStat, KU Leuven, Leuven, Belgium.ORCID https://orcid.org/0000-0003-2364-7555
Ariel Alonso AbadL-BioStat, KU Leuven, Leuven, Belgium.
Geert MolenberghsL-BioStat, KU Leuven, Leuven, Belgium.

Funding

Fonds Wetenschappelijk Onderzoek G0A4121N
6 · The paper itself

Abstract

In many studies, multiple longitudinal outcomes are collected, and interest lies in studying the association between these outcomes. Joint modeling is then required, but full likelihood estimation becomes infeasible as the number of outcomes increases. To address this, the pairwise-fitting approach was developed. However, the robustness of this pseudo-likelihood-based approach under missing at random (MAR) remains unclear. We investigate the impact of MAR dropout on the pairwise-fitting approach through a case and simulation study and compare the results to full likelihood estimation. In the simulation study, we simulate three continuous longitudinal outcomes so that full likelihood estimation remains computationally feasible, allowing a comparison with the pairwise fitting approach. Various settings are examined, including random intercept and random intercept-and-slope models, in which we vary the standard deviation of the error terms and the degree of correlation between random effects. Our results show that bias remains limited in random intercept models and in most random intercept-and-slope models. However, when the standard deviation of the error terms becomes large compared to that of the random effects, some bias appears in the covariances between the random effects of the outcomes not driving dropout. This bias is mitigated using multiple imputation. As a case study, we analyzed data from a schizophrenia study using both full likelihood and pseudo-likelihood approaches and compared the results.

Indexed as

Computer SimulationModels, StatisticalPatient DropoutsResearch DesignBiasData Interpretation, StatisticalHumansLikelihood FunctionsLongitudinal Studiesjoint modelingMARmultiple imputationmultivariate longitudinal datapairwise‐fitting approachpseudo‐likelihood

Identifiers

PMID42665560
PMCPMC13524844

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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.