TY - JOUR
T1 - Polybrominated dibenzo-p-dioxins, dibenzofurans, and biphenyls
T2 - Inclusion in the toxicity equivalency factor concept for dioxin-like compounds
AU - van den Berg, Martin
AU - Denison, Michael S.
AU - Birnbaum, Linda S.
AU - DeVito, Michael J.
AU - Fiedler, Heidelore
AU - Falandysz, Jerzy
AU - Rose, Martin
AU - Schrenk, Dieter
AU - Safe, Stephen
AU - Tohyama, Chiharu
AU - Tritscher, Angelika
AU - Tysklind, Mats
AU - Peterson, Richard E.
N1 - Funding Information:
This research has been supported by the United Nations Environment Programme, Chemicals Branch of Division of Technology, Industry and Economics, and the Intramural Research Program of the National Institutes of Health, NIEHS, and NCI.
PY - 2013/6
Y1 - 2013/6
N2 - In 2011, a joint World Health Organization (WHO) and United Nations Environment Programme (UNEP) expert consultation took place, during which the possible inclusion of brominated analogues of the dioxin-like compounds in the WHO Toxicity Equivalency Factor (TEF) scheme was evaluated. The expert panel concluded that polybrominated dibenzo-p-dioxins (PBDDs), dibenzofurans (PBDFs), and some dioxin-like biphenyls (dl-PBBs) may contribute significantly in daily human background exposure to the total dioxin toxic equivalencies (TEQs). These compounds are also commonly found in the aquatic environment. Available data for fish toxicity were evaluated for possible inclusion in the WHO-UNEP TEF scheme (van den Berg et al., 1998). Because of the limited database, it was decided not to derive specific WHO-UNEP TEFs for fish, but for ecotoxicological risk assessment, the use of specific relative effect potencies (REPs) from fish embryo assays is recommended. Based on the limited mammalian REP database for these brominated compounds, it was concluded that sufficient differentiation from the present TEF values of the chlorinated analogues (van den Berg et al., 2006) was not possible. However, the REPs for PBDDs, PBDFs, and non-ortho dl-PBBs in mammals closely follow those of the chlorinated analogues, at least within one order of magnitude. Therefore, the use of similar interim TEF values for brominated and chlorinated congeners for human risk assessment is recommended, pending more detailed information in the future.
AB - In 2011, a joint World Health Organization (WHO) and United Nations Environment Programme (UNEP) expert consultation took place, during which the possible inclusion of brominated analogues of the dioxin-like compounds in the WHO Toxicity Equivalency Factor (TEF) scheme was evaluated. The expert panel concluded that polybrominated dibenzo-p-dioxins (PBDDs), dibenzofurans (PBDFs), and some dioxin-like biphenyls (dl-PBBs) may contribute significantly in daily human background exposure to the total dioxin toxic equivalencies (TEQs). These compounds are also commonly found in the aquatic environment. Available data for fish toxicity were evaluated for possible inclusion in the WHO-UNEP TEF scheme (van den Berg et al., 1998). Because of the limited database, it was decided not to derive specific WHO-UNEP TEFs for fish, but for ecotoxicological risk assessment, the use of specific relative effect potencies (REPs) from fish embryo assays is recommended. Based on the limited mammalian REP database for these brominated compounds, it was concluded that sufficient differentiation from the present TEF values of the chlorinated analogues (van den Berg et al., 2006) was not possible. However, the REPs for PBDDs, PBDFs, and non-ortho dl-PBBs in mammals closely follow those of the chlorinated analogues, at least within one order of magnitude. Therefore, the use of similar interim TEF values for brominated and chlorinated congeners for human risk assessment is recommended, pending more detailed information in the future.
KW - Biomarkers
KW - Dioxin
KW - Halogenated hydrocarbon
KW - Persistent organic chemicals
KW - Polychlorinated biphenyls
KW - Regulatory/policy
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U2 - 10.1093/toxsci/kft070
DO - 10.1093/toxsci/kft070
M3 - Article
C2 - 23492812
AN - SCOPUS:84878492309
SN - 1096-6080
VL - 133
SP - 197
EP - 208
JO - Toxicological Sciences
JF - Toxicological Sciences
IS - 2
ER -