Bayesian hierarchical modeling for bivariate multiscale spatial data with application to blood test monitoring.
Change of support
Image segmentation
Regionalization
Simple areal interpolation
Spatial misalignment
Journal
Spatial and spatio-temporal epidemiology
ISSN: 1877-5853
Titre abrégé: Spat Spatiotemporal Epidemiol
Pays: Netherlands
ID NLM: 101516571
Informations de publication
Date de publication:
Aug 2024
Aug 2024
Historique:
received:
20
09
2023
revised:
09
05
2024
accepted:
14
05
2024
medline:
26
8
2024
pubmed:
26
8
2024
entrez:
24
8
2024
Statut:
ppublish
Résumé
Public health spatial data are often recorded at different spatial scales (or geographic regions/divisions) and over different correlated variables. Motivated by data from the Dartmouth Atlas Project, we consider jointly analyzing average annual percentages of diabetic Medicare enrollees who have taken the hemoglobin A1c and blood lipid tests, observed at the hospital service area (HSA) and county levels, respectively. Capitalizing on bivariate relationships between these two scales is not immediate as counties are not nested within HSAs. It is well known that one can improve predictions by leveraging correlations across both variables and scales. There are very few methods available that simultaneously model multivariate and multiscale correlations. We propose three new hierarchical Bayesian models for bivariate multiscale spatial data, extending spatial random effects, multivariate conditional autoregressive (MCAR), and ordered hierarchical models through a multiscale spatial approach. We simulated data from each of the three models and compared the corresponding predictions, and found the computationally intensive multiscale MCAR model is more robust to model misspecification. In an analysis of 2015 Texas Dartmouth Atlas Project data, we produced finer resolution predictions (partitioning of HSAs and counties) than univariate analyses, determined that the novel multiscale MCAR and OH models were preferable via out-of-sample metrics, and determined the HSA with the highest within-HSA variability of hemoglobin A1c blood testing. Additionally, we compare the univariate multiscale models to the bivariate multiscale models and see clear improvements in prediction over univariate analyses.
Identifiants
pubmed: 39181601
pii: S1877-5845(24)00028-5
doi: 10.1016/j.sste.2024.100661
pii:
doi:
Substances chimiques
Glycated Hemoglobin
0
Lipids
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
100661Informations de copyright
Copyright © 2024 Elsevier Ltd. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.