Estimation of Dose-Rate Effectiveness Factor for Malignant Tumor Mortality: Joint Analysis of Mouse Data Exposed to Chronic and Acute Radiation
Uncertainties due to confounding factors in epidemiological studies have limited our knowledge of the effects of low-dose-rate chronic exposure on human health. Animal experiments, wherein each subject is considered to be nearly identical, can complement the limitations of epidemiological studies. T...
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Published in | Radiation research Vol. 194; no. 5; p. 500 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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United States
10.11.2020
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Abstract | Uncertainties due to confounding factors in epidemiological studies have limited our knowledge of the effects of low-dose-rate chronic exposure on human health. Animal experiments, wherein each subject is considered to be nearly identical, can complement the limitations of epidemiological studies. Therefore, we conducted a joint analysis of previously published cancer mortality data in B6C3F1 female mice chronically and acutely irradiated with 137Cs γ rays to estimate the dose-rate effectiveness factor. In the chronically irradiated animal experiment conducted by the Institute for Environmental Sciences, mice received irradiation at dose rates of 0.05, 1.1 or 21 mGy per day for 400 days from 8 weeks of age. For the acutely irradiated animal experiment conducted by the National Institute of Radiological Sciences, mice received irradiation at 35, 105, 240 or 365 days of age with 1.9, 3.8 or 5.9 Gy at a dose rate of 0.98 Gy per min. Because the preliminary analyses suggested that the risk was dependent on the age at exposure, a model was applied that considered risk differences depending on this factor. The model analysis revealed a three-fold, significantly decreased risk per Gy in mice exposed to 21 mGy per day compared to that in acutely irradiated mice. This resulted in a dose-rate effectiveness factor larger than that reported previously. |
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AbstractList | Uncertainties due to confounding factors in epidemiological studies have limited our knowledge of the effects of low-dose-rate chronic exposure on human health. Animal experiments, wherein each subject is considered to be nearly identical, can complement the limitations of epidemiological studies. Therefore, we conducted a joint analysis of previously published cancer mortality data in B6C3F1 female mice chronically and acutely irradiated with 137Cs γ rays to estimate the dose-rate effectiveness factor. In the chronically irradiated animal experiment conducted by the Institute for Environmental Sciences, mice received irradiation at dose rates of 0.05, 1.1 or 21 mGy per day for 400 days from 8 weeks of age. For the acutely irradiated animal experiment conducted by the National Institute of Radiological Sciences, mice received irradiation at 35, 105, 240 or 365 days of age with 1.9, 3.8 or 5.9 Gy at a dose rate of 0.98 Gy per min. Because the preliminary analyses suggested that the risk was dependent on the age at exposure, a model was applied that considered risk differences depending on this factor. The model analysis revealed a three-fold, significantly decreased risk per Gy in mice exposed to 21 mGy per day compared to that in acutely irradiated mice. This resulted in a dose-rate effectiveness factor larger than that reported previously. |
Author | Suzuki, Keiji Imaoka, Tatsuhiko Sasatani, Megumi Yamada, Yutaka Tanaka, Satoshi Kai, Michiaki Kakinuma, Shizuko Doi, Kazutaka |
Author_xml | – sequence: 1 givenname: Kazutaka surname: Doi fullname: Doi, Kazutaka organization: Center for Radiation Protection Knowledge, National Institute of Radiological Sciences (NIRS), National Institutes for Quantum and Radiological Science and Technology (QST), Chiba, Japan – sequence: 2 givenname: Michiaki surname: Kai fullname: Kai, Michiaki organization: Environmental Health Science Division, Oita University of Nursing and Health Sciences, Oita, Japan – sequence: 3 givenname: Keiji surname: Suzuki fullname: Suzuki, Keiji organization: Atomic Bomb Disease Institute, Nagasaki University, Nagasaki, Japan – sequence: 4 givenname: Tatsuhiko surname: Imaoka fullname: Imaoka, Tatsuhiko organization: Department of Radiation Effects Research, National Institute of Radiological Sciences (NIRS), National Institutes for Quantum and Radiological Science and Technology (QST), Chiba, Japan – sequence: 5 givenname: Megumi surname: Sasatani fullname: Sasatani, Megumi organization: Department of Experimental Oncology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, Japan – sequence: 6 givenname: Satoshi surname: Tanaka fullname: Tanaka, Satoshi organization: Department of Radiobiology, Institute for Environmental Sciences, Aomori, Japan – sequence: 7 givenname: Yutaka surname: Yamada fullname: Yamada, Yutaka organization: Department of Radioecology and Fukushima Project, Center for Advanced Radiation Emergency Medicine, National Institute of Radiological Sciences (NIRS), National Institutes for Quantum and Radiological Science and Technology (QST), Chiba, Japan – sequence: 8 givenname: Shizuko surname: Kakinuma fullname: Kakinuma, Shizuko organization: Department of Radiation Effects Research, National Institute of Radiological Sciences (NIRS), National Institutes for Quantum and Radiological Science and Technology (QST), Chiba, Japan |
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SubjectTerms | Age Factors Animals Cesium Radioisotopes Crosses, Genetic Dose-Response Relationship, Radiation Female Gamma Rays - adverse effects Kaplan-Meier Estimate Mice Mice, Inbred C3H Mice, Inbred C57BL Models, Biological Neoplasms, Radiation-Induced - mortality Radiation Exposure - adverse effects Risk Specific Pathogen-Free Organisms |
Title | Estimation of Dose-Rate Effectiveness Factor for Malignant Tumor Mortality: Joint Analysis of Mouse Data Exposed to Chronic and Acute Radiation |
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