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Zero-inflated spatio-temporal models for disease mapping.

Mahmoud Torabi1

  • 1Department of Community Health Sciences, University of Manitoba, Winnipeg, MB R3E 0W3, Canada.

Biometrical Journal. Biometrische Zeitschrift
|February 11, 2017
PubMed
Summary
This summary is machine-generated.

This study analyzes disease incidence using zero-inflated spatio-temporal models. The data cloning method offers a computationally convenient frequentist approach for analyzing excess zeros in disease data.

Keywords:
Bayesian computationHierarchical modelsRandom effectsSpatial modelsSplineZero inflated models

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Area of Science:

  • Biostatistics
  • Epidemiology
  • Spatial Statistics

Background:

  • Spatio-temporal disease incidence data often exhibit excess zeros, complicating standard statistical modeling.
  • Traditional frequentist analysis of complex spatio-temporal models with random effects is computationally intensive.
  • Bayesian methods using Markov chain Monte Carlo (MCMC) offer computational convenience but may not align with frequentist objectives.

Purpose of the Study:

  • To analyze geographical and temporal variability of disease incidence in spatio-temporal count data with excess zeros.
  • To propose and evaluate a frequentist approach for zero-inflated spatio-temporal modeling using data cloning.
  • To facilitate computationally convenient estimation and prediction for disease incidence patterns.

Main Methods:

  • Utilized zero-inflated Poisson models with random effects to account for excess zeros.
  • Employed spatio-temporal models incorporating conditionally autoregressive (CAR) spatial smoothing and B-spline temporal smoothing.
  • Applied the data cloning (DC) method for computationally convenient frequentist analysis, yielding maximum likelihood estimates.

Main Results:

  • The data cloning approach provides a computationally feasible frequentist method for zero-inflated spatio-temporal disease modeling.
  • This method facilitates straightforward prediction and calculation of standard errors or prediction intervals for disease incidence.
  • The approach was successfully illustrated using real-world monthly pediatric asthma hospital visit data from Manitoba, Canada.

Conclusions:

  • The proposed data cloning method offers an effective frequentist solution for analyzing spatio-temporal disease data with excess zeros.
  • This approach enhances the ability to understand and predict geographical and temporal disease incidence patterns.
  • The study demonstrates the utility of data cloning in complex epidemiological modeling.