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Background: INTEROCC is a seven-country cohort study of occupational exposures and brain cancer risk, including occupational exposure to electromagnetic fields (EMF). In the absence of data on individual exposures, a Job Exposure Matrix (JEM) may be used to construct likely exposure scenarios in occupational settings. This tool was constructed using statistical summaries of exposure to EMF for various occupational categories for a comparable group of workers.
Methods: In this study, we use the Canadian data from INTEROCC to determine the best EMF exposure surrogate/estimate from three appropriately chosen surrogates from the JEM, along with a fourth surrogate based on Berkson error adjustments obtained via numerical approximation of the likelihood function. In this article, we examine the case in which exposures are gamma-distributed for each occupation in the JEM, as an alternative to the log-normal exposure distribution considered in a previous study conducted by our research team. We also study using those surrogates and the Berkson error adjustment in Poisson regression and conditional logistic regression.
Results: Simulations show that the introduced methods of Berkson error adjustment for non-stratified analyses provide accurate estimates of the risk of developing tumors in case of gamma exposure model. Alternatively, and under some technical assumptions, the arithmetic mean is the best surrogate when a gamma-distribution is used as an exposure model. Simulations also show that none of the present methods could provide an accurate estimate of the risk in case of stratified analyses.
Conclusion: While our previous study found the geometric mean to be the best exposure surrogate, the present study suggests that the best surrogate is dependent on the exposure model; the arithmetic means in case of gamma-exposure model and the geometric means in case of log-normal exposure model. However, we could present a better method of Berkson error adjustment for each of the two exposure models. Our results provide useful guidance on the application of JEMs for occupational exposure assessments, with adjustment for Berkson error.
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http://dx.doi.org/10.1186/s12874-023-02044-x | DOI Listing |
Int J Radiat Biol
September 2025
Department of Epidemiology and Biostatistics, School of Medicine, University of California, San Francisco, CA, USA.
Purpose: Low-dose radiation risks are generally extrapolated from groups exposed at high levels of dose. Measurement error substantially alters dose-response shape and hence extrapolated risk. Much attention has been paid to methods of dealing with shared errors, common in many datasets, in particular using Bayesian model averaging (BMA) methods.
View Article and Find Full Text PDFIntroduction: Cohort studies have been widely used to estimate the effects of long-term exposure to air pollutants on health outcomes. The nature of the exposure (i.e.
View Article and Find Full Text PDFSpat Spatiotemporal Epidemiol
June 2025
Department of Biostatistics and Bioinformatics, Emory Rollins School of Public Health, Atlanta, GA, USA.
Monitoring small-area geographical population trends in opioid mortality has significant implications for informing preventative resource allocation. A common approach to estimating small-area opioid mortality uses a standard disease mapping method where population-at-risk estimates (denominators) are treated as fixed. This assumption ignores the uncertainty in small-area population estimates, potentially biasing risk estimates and underestimating their uncertainties.
View Article and Find Full Text PDFInt J Radiat Biol
September 2024
Department of Epidemiology and Biostatistics, Indiana University School of Public Health, Bloomington, IN, USA.
Purpose: Epidemiological studies of stochastic radiation health effects such as cancer, meant to estimate risks of the adverse effects as a function of radiation dose, depend largely on estimates of the radiation doses received by the exposed group under study. Those estimates are based on dosimetry that always has uncertainty, which often can be quite substantial. Studies that do not incorporate statistical methods to correct for dosimetric uncertainty may produce biased estimates of risk and incorrect confidence bounds on those estimates.
View Article and Find Full Text PDFSci Rep
March 2024
Department of Epidemiology and Biostatistics, School of Medicine, University of California, San Francisco, 550 16th Street, 2nd Floor, San Francisco, CA, 94143, USA.
For many cancer sites low-dose risks are not known and must be extrapolated from those observed in groups exposed at much higher levels of dose. Measurement error can substantially alter the dose-response shape and hence the extrapolated risk. Even in studies with direct measurement of low-dose exposures measurement error could be substantial in relation to the size of the dose estimates and thereby distort population risk estimates.
View Article and Find Full Text PDF