Oana Petrof, Thomas Neyens, Maren Vranckx, Valerie Nuyts, Kristiaan Nackaerts, Benoit Nemery, Christel Faes
Traditional disease mapping models are based on relating the observed number of disease cases per spatially discrete area to an expected number of cases for that area. Expected numbers are calculated by internal standardisation, which requires both accurate population numbers and disease rates per age group. Con dentiality issues or the absence of high-quality information about the characteristics of a population-at-risk can hamper those calculations. Based on methods in point process analysis, we propose the use of a case-control approach in the context of lattice data, in which an unrelated spatially unstructured disease is used as a control disease. We apply our methods to a Belgian study of mesothelioma risk, where pancreatic cancer serves as the control disease. The analysis results are in close agreement with those coming from traditional disease mapping models based on internally standardised expected counts.
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