Evidence map›Paper›PMID 27908590›Full record

ArticleAnnals of epidemiology2017

Disease mapping of zero-excessive mesothelioma data in Flanders.

Thomas Neyens, Andrew B Lawson, Russell S Kirby, Valerie Nuyts, Kevin Watjou, Mehreteab Aregay, Rachel Carroll, Tim S Nawrot, Christel Faes

Abstract read
In one paragraph

Article in Annals of epidemiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Asbestos Exposure and the Mesothelioma Incidence in Poland.International journal of environmental research and public health · 2018
    Article
  4. Article
  5. Article
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

9 authors.

Thomas NeyensDepartment of Sciences, I-BioStat, University of Hasselt, Hasselt, Belgium. Electronic address: thomas.neyens@uhasselt.be.
Andrew B LawsonDivision of Biostatistics and Bioinformatics, Department of Public Health Sciences, Medical University of South Carolina, Charleston.
Russell S KirbyDepartment of Community and Family Health, College of Public Health, University of South Florida, Tampa.
Valerie NuytsDepartment of Public Health and Primary Care, Centre for Environment and Health, KU Leuven, Leuven, Belgium.
Kevin WatjouDepartment of Sciences, I-BioStat, University of Hasselt, Hasselt, Belgium.
Mehreteab AregayDivision of Biostatistics and Bioinformatics, Department of Public Health Sciences, Medical University of South Carolina, Charleston.
Rachel CarrollDivision of Biostatistics and Bioinformatics, Department of Public Health Sciences, Medical University of South Carolina, Charleston.
Tim S NawrotDepartment of Public Health and Primary Care, Centre for Environment and Health, KU Leuven, Leuven, Belgium; Department of Sciences, Centre for Environmental Sciences, University of Hasselt, Hasselt, Belgium.
Christel FaesDepartment of Sciences, I-BioStat, University of Hasselt, Hasselt, Belgium.

Funding

Uncertainty in spatial health analysis due to missingness and aggregation effectsR01CA172805 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI FAES, CHRISTEL MARIA JORIS, KIRBY, RUSSELL S. · 2013 to 2015
$886k
NCI NIH HHS R01 CA172805
6 · The paper itself

Abstract

purposeTo investigate the distribution of mesothelioma in Flanders using Bayesian disease mapping models that account for both an excess of zeros and overdispersion.

methodsThe numbers of newly diagnosed mesothelioma cases within all Flemish municipalities between 1999 and 2008 were obtained from the Belgian Cancer Registry. To deal with overdispersion, zero inflation, and geographical association, the hurdle combined model was proposed, which has three components: a Bernoulli zero-inflation mixture component to account for excess zeros, a gamma random effect to adjust for overdispersion, and a normal conditional autoregressive random effect to attribute spatial association. This model was compared with other existing methods in literature.

resultsThe results indicate that hurdle models with a random effects term accounting for extra variance in the Bernoulli zero-inflation component fit the data better than hurdle models that do not take overdispersion in the occurrence of zeros into account. Furthermore, traditional models that do not take into account excessive zeros but contain at least one random effects term that models extra variance in the counts have better fits compared to their hurdle counterparts. In other words, the extra variability, due to an excess of zeros, can be accommodated by spatially structured and/or unstructured random effects in a Poisson model such that the hurdle mixture model is not necessary.

conclusionsModels taking into account zero inflation do not always provide better fits to data with excessive zeros than less complex models. In this study, a simple conditional autoregressive model identified a cluster in mesothelioma cases near a former asbestos processing plant (Kapelle-op-den-Bos). This observation is likely linked with historical local asbestos exposures. Future research will clarify this.

Indexed as

RegistriesAdultAgedAge DistributionBayes TheoremBelgiumFemaleGeographic MappingHumansIncidenceLung NeoplasmsMaleMesotheliomaMesothelioma, MalignantMiddle AgedPericardiumBayesian analysisConditional autoregressive convolution modelDisease mappingExcess zerosMesothelioma

Identifiers

PMID27908590
PMCPMC5272833

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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.