Evidence map›Paper›PMID 33728679›Full record

ArticleStatistics in medicine2021

A Bayesian approach for estimating age-adjusted rates for low-prevalence diseases over space and time.

Melissa Jay, Jacob Oleson, Mary Charlton, Ali Arab

Abstract read
In one paragraph

Article in Statistics in medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Spatiotemporal Modeling Approach to Mapping Geographic and Temporal Variation in Cancer Incidence Rates for US Counties.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Melissa JayDepartment of Biostatistics, The University of Iowa, Iowa City, Iowa, USA.ORCID 0000-0002-8740-4803
Jacob OlesonDepartment of Biostatistics, The University of Iowa, Iowa City, Iowa, USA.
Mary CharltonDepartment of Epidemiology, The University of Iowa, Iowa City, Iowa, USA.
Ali ArabDepartment of Mathematics and Statistics, Georgetown University, Washington, District of Columbia, USA.

Funding

Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI Jong Sung Kim · 1990 to 2026
$40.5M
NIEHS NIH HHS P30 ES005605
6 · The paper itself

Abstract

Age-adjusted rates are frequently used by epidemiologists to compare disease incidence and mortality across populations. In small geographic regions, age-adjusted rates computed directly from the data are subject to considerable variability and are generally unreliable. Therefore, we desire an approach that accounts for the excessive number of zero counts in disease mapping datasets, which are naturally present for low-prevalence diseases and are further innated when stratifying by age group. Bayesian modeling approaches are naturally suited to employ spatial and temporal smoothing to produce more stable estimates of age-adjusted rates for small areas. We propose a Bayesian hierarchical spatio-temporal hurdle model for counts and demonstrate how age-adjusted rates can be estimated from the hurdle model. We perform a simulation study to evaluate the performance of the proposed model vs a traditional Poisson model on datasets with varying characteristics. The approach is illustrated using two applications to cancer mortality at the county level.

Indexed as

Bayes TheoremComputer SimulationHumansPrevalencecancerdisease mappinghurdleriskstandardization

Identifiers

PMID33728679
PMCPMC9575652

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Registered trials

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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.