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Geographical clustering of prostate cancer grade and stage at diagnosis, before and after adjustment for risk factors

BACKGROUND: Spatial variation in patterns of disease outcomes is often explored with techniques such as cluster detection analysis. In other types of investigations, geographically varying individual or community level characteristics are often used as independent predictors in statistical models wh...

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Autores principales: Klassen, Ann Carroll, Kulldorff, Martin, Curriero, Frank
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC546220/
https://www.ncbi.nlm.nih.gov/pubmed/15649329
http://dx.doi.org/10.1186/1476-072X-4-1
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author Klassen, Ann Carroll
Kulldorff, Martin
Curriero, Frank
author_facet Klassen, Ann Carroll
Kulldorff, Martin
Curriero, Frank
author_sort Klassen, Ann Carroll
collection PubMed
description BACKGROUND: Spatial variation in patterns of disease outcomes is often explored with techniques such as cluster detection analysis. In other types of investigations, geographically varying individual or community level characteristics are often used as independent predictors in statistical models which also attempt to explain variation in disease outcomes. However, there is a lack of research which combines geographically referenced exploratory analysis with multilevel models. We used a spatial scan statistic approach, in combination with predicted block group-level disease patterns from multilevel models, to examine geographic variation in prostate cancer grade and stage at diagnosis. RESULTS: We examined data from 20928 Maryland men with incident prostate cancer reported to the Maryland Cancer Registry during 1992–1997. Initial cluster detection analyses, prior to adjustment, indicated that there were four statistically significant clusters of high and low rates of each outcome (later stage at diagnosis and higher histologic grade of tumor) for prostate cancer cases in Maryland during 1992–1997. After adjustment for individual case attributes, including age, race, year of diagnosis, patterns of clusters changed for both outcomes. Additional adjustment for Census block group and county-level socioeconomic measures changed the cluster patterns further. CONCLUSIONS: These findings provide evidence that, in locations where adjustment changed patterns of clusters, the adjustment factors may be contributing causes of the original clusters. In addition, clusters identified after adjusting for individual and area-level predictors indicate area of unexplained variation, and merit further small-area investigations.
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spelling pubmed-5462202005-01-30 Geographical clustering of prostate cancer grade and stage at diagnosis, before and after adjustment for risk factors Klassen, Ann Carroll Kulldorff, Martin Curriero, Frank Int J Health Geogr Research BACKGROUND: Spatial variation in patterns of disease outcomes is often explored with techniques such as cluster detection analysis. In other types of investigations, geographically varying individual or community level characteristics are often used as independent predictors in statistical models which also attempt to explain variation in disease outcomes. However, there is a lack of research which combines geographically referenced exploratory analysis with multilevel models. We used a spatial scan statistic approach, in combination with predicted block group-level disease patterns from multilevel models, to examine geographic variation in prostate cancer grade and stage at diagnosis. RESULTS: We examined data from 20928 Maryland men with incident prostate cancer reported to the Maryland Cancer Registry during 1992–1997. Initial cluster detection analyses, prior to adjustment, indicated that there were four statistically significant clusters of high and low rates of each outcome (later stage at diagnosis and higher histologic grade of tumor) for prostate cancer cases in Maryland during 1992–1997. After adjustment for individual case attributes, including age, race, year of diagnosis, patterns of clusters changed for both outcomes. Additional adjustment for Census block group and county-level socioeconomic measures changed the cluster patterns further. CONCLUSIONS: These findings provide evidence that, in locations where adjustment changed patterns of clusters, the adjustment factors may be contributing causes of the original clusters. In addition, clusters identified after adjusting for individual and area-level predictors indicate area of unexplained variation, and merit further small-area investigations. BioMed Central 2005-01-13 /pmc/articles/PMC546220/ /pubmed/15649329 http://dx.doi.org/10.1186/1476-072X-4-1 Text en Copyright © 2005 Klassen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Klassen, Ann Carroll
Kulldorff, Martin
Curriero, Frank
Geographical clustering of prostate cancer grade and stage at diagnosis, before and after adjustment for risk factors
title Geographical clustering of prostate cancer grade and stage at diagnosis, before and after adjustment for risk factors
title_full Geographical clustering of prostate cancer grade and stage at diagnosis, before and after adjustment for risk factors
title_fullStr Geographical clustering of prostate cancer grade and stage at diagnosis, before and after adjustment for risk factors
title_full_unstemmed Geographical clustering of prostate cancer grade and stage at diagnosis, before and after adjustment for risk factors
title_short Geographical clustering of prostate cancer grade and stage at diagnosis, before and after adjustment for risk factors
title_sort geographical clustering of prostate cancer grade and stage at diagnosis, before and after adjustment for risk factors
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC546220/
https://www.ncbi.nlm.nih.gov/pubmed/15649329
http://dx.doi.org/10.1186/1476-072X-4-1
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