dc.contributor.author | Liu-Mares, W | |
dc.contributor.author | Mackinnon, JA | |
dc.contributor.author | Sherman, R | |
dc.contributor.author | Fleming, LE | |
dc.contributor.author | Rocha-Lima, C | |
dc.contributor.author | Hu, JJ | |
dc.contributor.author | Lee, DJ | |
dc.date.accessioned | 2018-01-02T10:21:46Z | |
dc.date.issued | 2013-03-12 | |
dc.description.abstract | BACKGROUND: We sought to identify high-risk areas of pancreatic cancer incidence, and determine if clusters of persons diagnosed with pancreatic cancer were more likely to be located near arsenic-contaminated drinking water wells. METHODS: A total of 5,707 arsenic samples were collected from December 2000 to May 2008 by the Florida Department of Health, representing more than 5,000 individual privately owned wells. During that period, 0.010 ppm (10 ppb) or greater arsenic levels in private well water were considered as the threshold based on standard of United States Environmental Protection Agency (EPA). Spatial modeling was applied to pancreatic cancer cases diagnosed between 1998-2002 in Florida (n = 11,405). Multivariable logistic regression was used to determine if sociodemographic indicators, smoking history, and proximity to arsenic-contaminated well sites were associated with residence at the time of pancreatic cancer diagnosis occurring within versus outside a cluster. RESULTS: Spatial modeling identified 16 clusters in which 22.6% of all pancreatic cancer cases were located. Cases living within 1 mile of known arsenic-contaminated wells were significantly more likely to be diagnosed within a cluster of pancreatic cancers relative to cases living more than 3 miles from known sites (odds ratio = 2.1 [95% CI = 1.9, 2.4]). CONCLUSIONS: Exposure to arsenic-contaminated drinking water wells may be associated with an increased risk of pancreatic cancer. However, case-control studies are needed in order to confirm the findings of this ecological analysis. These cluster areas may be appropriate to evaluate pancreatic cancer risk factors, and to perform targeted screening and prevention studies. | en_GB |
dc.description.sponsorship | The project was supported by grants from the James and Esther King Biomedical Research Foundation (#06TSP); the Bankhead-Coley Cancer Research Program (#1BG06-341963, #08BN-03), the Florida Department of Health (FDOH); the CDC National Program of Cancer Registries (CDC NPCR); and the European Union ERDF funding (University of Exeter). | en_GB |
dc.identifier.citation | Vol. 13, article 111 | en_GB |
dc.identifier.doi | 10.1186/1471-2407-13-111 | |
dc.identifier.uri | http://hdl.handle.net/10871/30771 | |
dc.language.iso | en | en_GB |
dc.publisher | BioMed Central | en_GB |
dc.relation.url | https://www.ncbi.nlm.nih.gov/pubmed/23510413 | en_GB |
dc.rights | © Liu-Mares et al; licensee BioMed Central Ltd. 2013. This article is published under license to BioMed Central Ltd. 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. | en_GB |
dc.subject | Adolescent | en_GB |
dc.subject | Adult | en_GB |
dc.subject | Aged | en_GB |
dc.subject | Aged, 80 and over | en_GB |
dc.subject | Arsenic | en_GB |
dc.subject | Cluster Analysis | en_GB |
dc.subject | Drinking Water | en_GB |
dc.subject | Environmental Exposure | en_GB |
dc.subject | Female | en_GB |
dc.subject | Florida | en_GB |
dc.subject | Humans | en_GB |
dc.subject | Incidence | en_GB |
dc.subject | Logistic Models | en_GB |
dc.subject | Male | en_GB |
dc.subject | Middle Aged | en_GB |
dc.subject | Pancreatic Neoplasms | en_GB |
dc.subject | Water Supply | en_GB |
dc.subject | Young Adult | en_GB |
dc.title | Pancreatic cancer clusters and arsenic-contaminated drinking water wells in Florida | en_GB |
dc.type | Article | en_GB |
dc.date.available | 2018-01-02T10:21:46Z | |
exeter.place-of-publication | England | en_GB |
dc.description | This is the final version of the article. Available from BioMed Central via the DOI in this record. | en_GB |
dc.identifier.journal | BMC Cancer | en_GB |