Evidence map›Paper›PMID 28587592›Full record

ArticleBMC medical research methodology2017

Bayesian hierarchical piecewise regression models: a tool to detect trajectory divergence between groups in long-term observational studies.

Marie-Jeanne Buscot, Simon S Wotherspoon, Costan G Magnussen, Markus Juonala, Matthew A Sabin, David P Burgner, Terho Lehtimäki, Jorma S A Viikari, Nina Hutri-Kähönen, Olli T Raitakari and 1 more

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Article in BMC medical research methodology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

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7citing 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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7 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Marie-Jeanne BuscotMenzies Institute for Medical Research, University of Tasmania, Hobart, Australia.
Simon S WotherspoonInstitute of Marine and Antarctic Studies, University of Tasmania, Hobart, Australia.
Costan G MagnussenMenzies Institute for Medical Research, University of Tasmania, Hobart, Australia.
Markus JuonalaResearch Centre of Applied and Preventive Cardiovascular Medicine, University of Turku, Turku, Finland.
Matthew A SabinMurdoch Childrens Research Institute, The Royal Children's Hospital, Melbourne, Australia.
David P BurgnerMurdoch Childrens Research Institute, The Royal Children's Hospital, Melbourne, Australia.
Terho LehtimäkiDepartment of Clinical Chemistry, Fimlab Ltd and University of Tampere School of Medicine, Tampere, Finland.
Jorma S A ViikariResearch Centre of Applied and Preventive Cardiovascular Medicine, University of Turku, Turku, Finland.
Nina Hutri-KähönenDepartment of Pediatrics, University of Tampere School of Medicine, Tampere, Finland.
Olli T RaitakariResearch Centre of Applied and Preventive Cardiovascular Medicine, University of Turku, Turku, Finland.
Russell J ThomsonCentre for Research in Mathematics, School of Computing, Engineering & Mathematics, Western Sydney University, Sydney, Australia. russell.thomson@westernsydney.edu.au.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBayesian hierarchical piecewise regression (BHPR) modeling has not been previously formulated to detect and characterise the mechanism of trajectory divergence between groups of participants that have longitudinal responses with distinct developmental phases. These models are useful when participants in a prospective cohort study are grouped according to a distal dichotomous health outcome. Indeed, a refined understanding of how deleterious risk factor profiles develop across the life-course may help inform early-life interventions. Previous techniques to determine between-group differences in risk factors at each age may result in biased estimate of the age at divergence.

methodsWe demonstrate the use of Bayesian hierarchical piecewise regression (BHPR) to generate a point estimate and credible interval for the age at which trajectories diverge between groups for continuous outcome measures that exhibit non-linear within-person response profiles over time. We illustrate our approach by modeling the divergence in childhood-to-adulthood body mass index (BMI) trajectories between two groups of adults with/without type 2 diabetes mellitus (T2DM) in the Cardiovascular Risk in Young Finns Study (YFS).

resultsUsing the proposed BHPR approach, we estimated the BMI profiles of participants with T2DM diverged from healthy participants at age 16 years for males (95% credible interval (CI):13.5-18 years) and 21 years for females (95% CI: 19.5-23 years). These data suggest that a critical window for weight management intervention in preventing T2DM might exist before the age when BMI growth rate is naturally expected to decrease. Simulation showed that when using pairwise comparison of least-square means from categorical mixed models, smaller sample sizes tended to conclude a later age of divergence. In contrast, the point estimate of the divergence time is not biased by sample size when using the proposed BHPR method.

conclusionsBHPR is a powerful analytic tool to model long-term non-linear longitudinal outcomes, enabling the identification of the age at which risk factor trajectories diverge between groups of participants. The method is suitable for the analysis of unbalanced longitudinal data, with only a limited number of repeated measures per participants and where the time-related outcome is typically marked by transitional changes or by distinct phases of change over time.

Indexed as

AlgorithmsBayes TheoremRegression AnalysisAdolescentBody Mass IndexBody WeightCardiovascular DiseasesDiabetes Mellitus, Type 2FemaleHumansMaleModels, StatisticalObservational Studies as TopicRisk FactorsTime FactorsYoung AdultAccelerated longitudinal designCohort effectGroup divergenceHierarchical regressionNon-linear trajectory modelPiecewise model

Identifiers

PMID28587592
PMCPMC5461770

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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.