Evidence map›Paper›PMID 39695379›Full record

ArticleBMC medical research methodology2024

Robustness assessment of regressions using cluster analysis typologies: a bootstrap procedure with application in state sequence analysis.

Leonard Roth, Matthias Studer, Emilie Zuercher, Isabelle Peytremann-Bridevaux

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Article in BMC medical research methodology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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2 citing papers in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Leonard RothDepartment of Epidemiology and Health Systems, Centre for Primary Care and Public Health (Unisanté), University of Lausanne, Route de La Corniche 10, 1010, Lausanne, Switzerland. leonard.roth@unisante.ch.
Matthias StuderCentre LIVES, University of Geneva, Boulevard du Pont-d'Arve 40, 1205, Geneva, Switzerland.
Emilie ZuercherDepartment of Epidemiology and Health Systems, Centre for Primary Care and Public Health (Unisanté), University of Lausanne, Route de La Corniche 10, 1010, Lausanne, Switzerland.
Isabelle Peytremann-BridevauxDepartment of Epidemiology and Health Systems, Centre for Primary Care and Public Health (Unisanté), University of Lausanne, Route de La Corniche 10, 1010, Lausanne, Switzerland.

Funding

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung 10001A 204740
6 · The paper itself

Abstract

backgroundIn standard Sequence Analysis, similar trajectories are clustered together to create a typology of trajectories, which is then often used to evaluate the association between sequence patterns and covariates inside regression models. The sampling uncertainty, which affects both the derivation of the typology and the associated regressions, is typically ignored in this analysis, an oversight that may lead to wrong statistical conclusions. We propose utilising sampling variation to derive new estimates that further inform on the association of interest.

methodsWe introduce a novel procedure to assess the robustness of regression results obtained from the standard analysis. Bootstrap samples are drawn from the data, and for each bootstrap, a new typology replicating the original one is constructed, followed by the estimation of the corresponding regression models. The bootstrap estimates are then combined using a multilevel modelling framework that mimics a meta-analysis. The fitted values from this multilevel model allow to account for the sampling uncertainty in the inferential analysis. We illustrate the methodology by applying it to the study of healthcare utilisation trajectories in a Swiss cohort of diabetic patients.

resultsThe procedure provides robust estimates for an association of interest, along with 95% prediction intervals, representing the range of expected values if the clustering and associated regressions were performed on a new sample from the same underlying distribution. It also identifies central and borderline trajectories within each cluster. Regarding the illustrative application, while there was evidence of an association between regular lipid testing and subsequent healthcare utilisation patterns in the original analysis, this is not supported in the robustness assessment.

conclusionsInvestigating the relationship between trajectory patterns and covariates is of interest in many situations. However, it is a challenging task with potential pitfalls. Our Robustness Assessment of Regression using Cluster Analysis Typologies (RARCAT) may assist in ensuring the robustness of such association studies. The method is applicable wherever clustering is combined with regression analysis, so its relevance goes beyond State Sequence Analysis.

Indexed as

Models, StatisticalAlgorithmsCluster AnalysisData Interpretation, StatisticalDiabetes MellitusHumansRegression AnalysisAssociation studyBootstrapCluster analysisMultilevel modellingRegression analysisSampling uncertaintySampling variationSequence AnalysisStatistical inferenceTypology of trajectories

Identifiers

PMID39695379
PMCPMC11654397

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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.