Health effects of dioxins in Europe

Dioxins (including furans and dioxin-like PCBs) are a group of polychlorinated organic compounds with the same toxic mechanism. They are by-products of various industrial processes and combustion activities and are considered to be highly toxic.

Dioxins and dioxin-like PCBs are quantified by toxic equivalents (TEQs) representing the total toxicity compared to the most toxic compound, 2,3,7,8-Tetrachlorodibenzodioxin (TCDD). The power of toxicity is calculated with Toxic Equivalent Factors (TEFs), which allow the toxic potentials of each compound to be added up, in order to derive the TEQ of the mixture. Acute toxicity, leading for example to chlorakne or alteration of liver function, is only expected at very high doses. Long-term exposure to dioxins has been linked to effects on the immune system, the nervous system, the endocrine system and reproductive functions and is also known to cause tooth and bone defects, diabetes as well as several types of cancer (USEPA, 2003). The association between dioxins and cancer has been most consistent for non-Hodgkin’s lymphoma. IARC classified TCDD (2,3,7,8-Tetrachlorodibenzo-p-dioxin), as a “known human carcinogen” (IARC, 1997). All other dioxin-like compounds are classified as “likely to be carcinogenic to humans”.

This group of chemicals is selected in EBoDE because of their high toxicity and potential troubling exposures through e.g. mothers milk.

Selected health endpoints and exposure-response functions

In EBoDE, we have quantified the effect of exposure to dioxins and dioxin-like PCBs on cancer (all cancer types, mortality only). The non-fatal and non-cancer effects were not suited for health impact assessments due to difficulties in estimating the exposure-response relationships and the other input parameters necessary for estimating DALYs. Therefore, our estimates may underestimate the true dioxin-related burden of disease.

Leino et al. (2008) assumed a linear exposure-response relationship for excess cancers associated with dioxin intake. They estimated the health risk for toxicity equivalent intake assuming additivity of the toxicity of the different types of dioxins and all cancer cases to be lethal.

The EBoDE calculations use the Leino et al. (2008) approach, but the results have been corrected with an updated cancer slope factor 1×10-3 per pg/kg/d of dioxin intake of the U.S. Environmental Protection Agency (USEPA, 2003; NAS, 2006). The assumption that all cancers are lethal may lead to overestimation of the impacts.

The health endpoints considered in this project for dioxins and the corresponding exposure-response functions are summarized in Table 3-19 in section 3.12. YLD estimates in the table are based on the attributable fraction derived from the ERF using method 2A (see Figure 2-1), which is applied to the total YLD for all cancers as represented in the WHO database.

Exposure data

Dioxins and dioxin-like PCBs are persistent and bio-accumulating. The main exposure route for these chemicals is animal fat in nutrition, which accounts for about 90% of all exposure. Other routes, such as inhalation, play a minor role. In order to estimate health effects related to dioxin exposure, daily intake data were needed. This intake depends on eating habits, age, gender, body weight and food consumption. Often, breast feeding contributes to the highest intake of dioxins for humans in their life. Dioxins have a long half life. Therefore the development of health effects in humans depends not only on the daily intake, but also on the body burden accumulated over years. On average, the daily intake of dioxins and dioxin-like PCBs decreases, while the body burden increases with age.

The cancer slope factor is expressed for daily intake of adults. There are different ways to measure the daily intake, each with different limitations. Table 3-2 describes some different measurement methods and provides short information about their use and limitations.

TABLE 3-2. Different ways to measure daily intake of dioxins and dioxin-like PCBs.

	Type of measurement	Type of use	Specific limitations and uncertainties
A	Survey (questionnaire) on food consumption	Information on food consumption and about the content of dioxins in representative food samples allow modelling of daily intake	Results are modelled for an average population - food contamination and eating habits can differ on a large scale
B	Total diet studies	The total diet in a population group over a certain time period and dioxin in this food or representative food samples are measured.	Results are only relevant for the investigated groups and not necessarily representative for the whole population, sampling period influence the results.
C	Human biomonitoring Investigation of human milk or blood levels	Analyses of samples can show the body burden. Experimental scaling is used to convert observed biomonitoring results (blood) into daily intakes.	D-R function is based on daily intake. Human milk or blood samples are not widely available. Different fat content of the bodies influences the results.

In addition, in all these studies different compounds can be measured:

1. Only dioxins and furans;
2. dioxins, furans; and dioxin-like PCBs
3. dioxins, furans and dioxin-like PCBs as well as all other dioxin-like compounds detected as dioxin-like activity, expressed as TEQ in Bioassays (e.g. CALLUX).

In the EBoDE project, we have used national exposure data because there is no international comparable data source available. The different countries have used different methods to derive the daily intake values.

Table 3-3 provides a summary of the data and sources for dioxin. The specific data used in this project are summarized in Table 3-21 in section 3.12. For the EBoDE project daily intake data are expressed as Toxic Equivalent (TEQ), estimated using the Toxic Equivalent Factors (TEFs) as provided by WHO (Van den Berg et al. 1998). Even though later TEFs exist (Van den Berg et al., 2006; http://www.who.int/ipcs/assessment/tef_update/en/), we used the results of the 1998 review, because most available data have been calculated using these TEFs.

TABLE 3-3.: Summary of the sources of dioxin data. Explanation for A, B C see Table 3-2.

Countries	Population groups	Source	Sampling years	Compounds measured	Dioxin intake 2004 pg/kg bw/d
Belgium (A)	female 18-44 y adults 50-65 y adults	Bilau 2008 Bilau 2008 Calculated mean	2002–2006	Calux-all dioxin-like compounds1	2.1 1.7 1.9 (mean)
Finland (A)	all	Kiviranta et al 2005	2002	Dioxins+PCB	1.5
France (C)	30–65 y	Fréry et al. 2006	2004	Dioxins+PCB	2.32
Germany (A)	adults	Umweltbundesamt 2005	2003	Dioxins+PCB	2.0
Italy (A)	13–94 y	Fattore et al 2006	1997–2003	Dioxins+PCB	2.33
Netherlands (A+B)	adults	De Mul 2008	2004	Dioxins+PCB	1.04

¹ Belgium – Dioxin and all dioxin-like compounds are measured with Bioassay, only the sum of all dioxin-like compounds is given; the daily intake was calculated as mean of the 2 adult groups.

² France – daily intake calculated based on blood concentration of 27.7 WHO-TEQ pg/g blood fat.

³ Italy – daily intake were calculated using, for most dioxin and DL-PCB concentration data, a database available from the European Commission (Gallani et al., 2004).

⁴ Netherlands – Values in the study were calculated using TEFs from 2005. For comparability, we have adjusted the values as presented by Mul et al (2008) by adapting the results to TEF 1998 adding 10%.