Published March 23, 2015 | Version v1
Journal article

Shared dosimetry error in epidemiological dose-response analyses

  • 1. Univ. of Southern California, Los Angeles, CA (United States)
  • 2. Hirosoft International, Eureka, CA (United States)
  • 3. Southern Urals Biophysics Institute, Ozersk (Russian Federation)
  • 4. Pacific Northwest National Lab. (PNNL), Richland, WA (United States)
  • 5. Fred Hutchinson Cancer Center, Seattle, WA (United States)
  • 6. Vanderbilt Univ., Nashville, TN (United States)
  • 7. U.S. Dept. of Energy, New York, NY (United States)
  • 8. Risk Assessment Corporation, Neeses, SC (United States)
  • 9. National Cancer Institute, Rockville, MD (United States)
  • 10. Leibniz Institute for Prevention Research and Epidemiology (Germany)

Description

Radiation dose reconstruction systems for large-scale epidemiological studies are sophisticated both in providing estimates of dose and in representing dosimetry uncertainty. For example, a computer program was used by the Hanford Thyroid Disease Study to provide 100 realizations of possible dose to study participants. The variation in realizations reflected the range of possible dose for each cohort member consistent with the data on dose determinates in the cohort. Another example is the Mayak Worker Dosimetry System 2013 which estimates both external and internal exposures and provides multiple realizations of 'possible' dose history to workers given dose determinants. This paper takes up the problem of dealing with complex dosimetry systems that provide multiple realizations of dose in an epidemiologic analysis. In this paper we derive expected scores and the information matrix for a model used widely in radiation epidemiology, namely the linear excess relative risk (ERR) model that allows for a linear dose response (risk in relation to radiation) and distinguishes between modifiers of background rates and of the excess risk due to exposure. We show that treating the mean dose for each individual (calculated by averaging over the realizations) as if it was true dose (ignoring both shared and unshared dosimetry errors) gives asymptotically unbiased estimates (i.e. the score has expectation zero) and valid tests of the null hypothesis that the ERR slope β is zero. Although the score is unbiased the information matrix (and hence the standard errors of the estimate of β) is biased for β≠0 when ignoring errors in dose estimates, and we show how to adjust the information matrix to remove this bias, using the multiple realizations of dose. The use of these methods in the context of several studies including, the Mayak Worker Cohort, and the U.S. Atomic Veterans Study, is discussed

Availability note (English)

Available from: DOI:10.1371/journal.pone.0119418 ; DOE Accepted Manuscript full text, or the publishers Best Available Version will be available free of charge after the embargo period from OSTI using http://www.osti.gov/pages/biblio/1193633

Additional details

Publishing Information

Journal Title
PloS One
Journal Volume
10
Journal Issue
3
Journal Page Range
vp.
ISSN
1932-6203

INIS

Country of Publication
United States
Country of Input or Organization
United States
INIS RN
47075051
Subject category
S61: RADIATION PROTECTION AND DOSIMETRY;
Descriptors DEI
BIOLOGICAL RADIATION EFFECTS; DOSE-RESPONSE RELATIONSHIPS; DOSIMETRY; EPIDEMIOLOGY; ERRORS; RADIATION DOSES; THYROID
Descriptors DEC
BIOLOGICAL EFFECTS; BODY; DOSES; ENDOCRINE GLANDS; GLANDS; ORGANS; RADIATION EFFECTS

Optional Information

Contract/Grant/Project number
HS0000091; SC0008944
Funding organization
USDOE (United States)
Secondary number(s)
OSTIID--1193633