» Articles » PMID: 24018838

Mapping Disease at an Approximated Individual Level Using Aggregate Data: a Case Study of Mapping New Hampshire Birth Defects

Overview
Publisher MDPI
Date 2013 Sep 11
PMID 24018838
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Limited by data availability, most disease maps in the literature are for relatively large and subjectively-defined areal units, which are subject to problems associated with polygon maps. High resolution maps based on objective spatial units are needed to more precisely detect associations between disease and environmental factors.

Method: We propose to use a Restricted and Controlled Monte Carlo (RCMC) process to disaggregate polygon-level location data to achieve mapping aggregate data at an approximated individual level. RCMC assigns a random point location to a polygon-level location, in which the randomization is restricted by the polygon and controlled by the background (e.g., population at risk). RCMC allows analytical processes designed for individual data to be applied, and generates high-resolution raster maps.

Results: We applied RCMC to the town-level birth defect data for New Hampshire and generated raster maps at the resolution of 100 m. Besides the map of significance of birth defect risk represented by p-value, the output also includes a map of spatial uncertainty and a map of hot spots.

Conclusions: RCMC is an effective method to disaggregate aggregate data. An RCMC-based disease mapping maximizes the use of available spatial information, and explicitly estimates the spatial uncertainty resulting from aggregation.

Citing Articles

Assessing the influence of the modifiable areal unit problem on Bayesian disease mapping in Queensland, Australia.

Jahan F, Haque S, Hogg J, Price A, Hassan C, Areed W PLoS One. 2025; 20(1):e0313079.

PMID: 39874284 PMC: 11774366. DOI: 10.1371/journal.pone.0313079.


A multi-constraint Monte Carlo Simulation approach to downscaling cancer data.

Liu L, Cowan L, Wang F, Onega T Health Place. 2025; 91:103411.

PMID: 39764879 PMC: 11788035. DOI: 10.1016/j.healthplace.2024.103411.


Evaluating Geographic Health Disparities in Cancer Care: Example of the Modifiable Areal Unit Problem.

Fontanet C, Carlos H, Weiss J, Diaz M, Shi X, Onega T Ann Surg Oncol. 2023; 30(12):6987-6989.

PMID: 37658267 PMC: 11166173. DOI: 10.1245/s10434-023-14140-9.


Spatiotemporal high-resolution prediction and mapping: methodology and application to dengue disease.

Jaya I, Folmer H J Geogr Syst. 2022; 24(4):527-581.

PMID: 35221792 PMC: 8857957. DOI: 10.1007/s10109-021-00368-0.


Spatial interaction between breast cancer and environmental pollution in the Monterrey Metropolitan Area.

Gasca-Sanchez F, Santuario-Facio S, Ortiz-Lopez R, Rojas-Martinez A, Mejia-Velazquez G, Garza-Perez E Heliyon. 2021; 7(9):e07915.

PMID: 34584999 PMC: 8450205. DOI: 10.1016/j.heliyon.2021.e07915.

References
1.
Openshaw S . Geographical information systems and tropical diseases. Trans R Soc Trop Med Hyg. 1996; 90(4):337-9. DOI: 10.1016/s0035-9203(96)90500-3. View

2.
Chi W, Wang J, Li X, Zheng X, Liao Y . Analysis of geographical clustering of birth defects in Heshun county, Shanxi province. Int J Environ Health Res. 2008; 18(4):243-52. DOI: 10.1080/09603120701824524. View

3.
Stallones L, Nuckols J, Berry J . Surveillance around hazardous waste sites: geographic information systems and reproductive outcomes. Environ Res. 1992; 59(1):81-92. DOI: 10.1016/s0013-9351(05)80227-0. View

4.
Wheeler D . A comparison of spatial clustering and cluster detection techniques for childhood leukemia incidence in Ohio, 1996-2003. Int J Health Geogr. 2007; 6:13. PMC: 1851703. DOI: 10.1186/1476-072X-6-13. View

5.
Oppong J, Tiwari C, Ruckthongsook W, Huddleston J, Arbona S . Mapping late testers for HIV in Texas. Health Place. 2012; 18(3):568-75. DOI: 10.1016/j.healthplace.2012.01.008. View