this chemical is not intentionally produced, it is a byproduct of another application
Found in these people:
Lexi Rome, Anonymous Adult 1, Charlotte Brody, Davis Baltz, Andrea Martin, Michael Lerner, Kathy Fowler, Sharyle Patton, Lucy Waletsky, U.S. Representative Louise Slaughter, Bill Moyers, Cord Blood Sample 18
Found in these locations:
Mill Valley, CA; Round Hill, VA; Berkeley, CA; Sausalito, CA; Bolinas, CA; Rockville, MD; Pleasantville, NY; Upstate New York, NY; NJ, USA
Laboratory animals. Dioxins cause toxicity to many organ systems in animals. Effects include liver and thyroid tumors; cardiovascular, skeletal, skin, immune, respiratory, neurological and reproductive toxicity; altered lipid and carbohydrate metabolism; reduced fertility and birth defects. Specific birth defects include reproductive tract and skeletal abnormalities, such as cleft palate (ATSDR 1998a). Dioxins are endocrine disruptors because they alter thyroid, reproductive, and adrenal hormone levels and function (ATSDR 1998a). Many of the lowest dose effects are developmental. For example, a one-time exposure to dioxin during fetal life can impair prostate development in male rats (Roman and Peterson 1998, Roman, et al. 1998, Timms, et al. 2002).
Humans. The effects of dioxins have been studied in humans who were exposed through diet, work, military service and industrial accidents. Dioxin (TCDD) is a known human carcinogen. It is associated with increased incidence of cancer in general and with non-Hodgkin's lymphoma and lung and soft-tissue cancer in particular (ATSDR 1998a, NTP 2002). Soft tissue includes muscle, fat, blood vessels or any of the other tissues that support, surround and protect organs of the body. Dioxin is also associated with non-cancer disorders including skin lesions (chloracne), and nervous system toxicity (ATSDR 1998a). Associations with other types of disorders are emerging. For example, recent follow-up of people exposed to an industrial explosion in Seveso, Italy (the highest known population exposure to TCDD) suggest that dioxin may also be associated with breast cancer (Warner, et al. 2002), menstrual irregularities (Eskenazi, et al. 2002), altered thyroid function, and diabetes (Kogevinas 2001). Risk of developing diabetes or glucose intolerance is also increased in military personnel who were exposed to dioxin-contaminated herbicide (Agent Orange) in the Vietnam War (Longnecker, et al. 2001). Although developmental effects of dioxin have not been adequately studied in humans, several studies have linked dioxin to altered sex ratio (in favor of females) (Mocarelli, et al. 2000).
In dioxin family of chemicals - pollutants from PVC production, industrial bleaching, incineration; cause cancer, may harm hormone system.
1,2,3,4,7,8-HxCDD (hexadioxin) has been found in 14 of the 34 people tested in EWG/Commonweal studies. It has also been found in 422 of the 2,547 people tested in CDC biomonitoring studies.
Top health concerns for 1,2,3,4,7,8-HxCDD (hexadioxin) (References)
|health concern or target organ||weight of evidence|
|Immune system (including sensitization and allergies)||limited|
|Birth defects and developmental delays||unknown|
Results for 1,2,3,4,7,8-HxCDD (hexadioxin)
in blood serum (lipid weight)
- geometric mean: 2 pg/g (lipid weight) in blood serum
- found in 14 of 34 people in the group
- geometric mean: 2.06 pg/g (lipid weight) in blood serum
- found in 422 of 2547 people in the group
|0||pg/g (lipid weight) in blood serum||61.5|
1,2,3,4,7,8-HxCDD (hexadioxin) results
Detailed toxicity classifications (References)
|Limited evidence in humans - immune system toxicity||ATSDR (1998). Toxicological profile for chlorinated dibenzo-o-dioxins (CDDs): Health effects chapter. http://www.atsdr.cdc.gov/toxprofiles/tp104.html|
|Birth defects - weight of evidence unknown/unassessed||ATSDR (1998). Toxicological profile for chlorinated dibenzo-o-dioxins (CDDs): Health effects chapter. http://www.atsdr.cdc.gov/toxprofiles/tp104.html|