Persistent organic pollutants and epidemic of diabetes and metabolic syndrome

Dear fellow diabetes investigators, you, myself and our Editorin-Chief, Dr Hotta, have the same goal; to do something about the epidemic of diabetes in Asia. I will not show the numbers again, as you have seen enough; simply there are too many people around us with diabetes. Why there are so many? Professor Eung-Jin Kim, Honorary President of Korean Diabetes Association, told me that diabetes was a rare disease in early 1960s. He saw only five cases of diabetes the whole year in 1957 at Seoul National University Hospital, which had 450 beds back then. It is clear that the diabetes epidemic in Korea (and elsewhere) is due to a change of the environment. Huge changes have occurred over the last half century in South Korea. She has industrialized, westernized and became wealthier. I do not believe industrialization is bad for South Koreans, as they live much longer now. Was the diabetes epidemic an inevitable consequence of these changes associated with industrialization? If it was, it might have been avoided. Something bad was introduced during the industrialization process; so-called persistent organic pollutants (POP). Recently, evidence supporting this conclusion has been forthcoming and is getting stronger. Persistent organic pollutants are defined as ‘chemical substances that persist in the environment, bio-accumulate through the food web, and pose a risk of causing adverse effects to human health and the environment’. The Stockholm Convention on POP, an organization formed by international treaty, identified 12 POP initially and then added nine POP later. Here is the list: pesticides (aldrin, chlordane, DDT, dieldrin, endrin, heptachlor, hexachlorobenzene, mirex, toxaphene, chlordecone, alpha hexachlorocyclohexane, beta hexachlorocyclohexane, lindane and pentachlorobenzene), industrial chemicals (hexachlorobenzene, polychlorinated biphenyls [PCB]; hexabromobiphenyl; hexabromodiphenyl ether and heptabromodiphenyl ether; pentachlorobenzene; perfluorooctane sulfonic acid, its salts and perfluorooctane sulfonyl fluoride; tetrabromodiphenyl ether and pentabromodiphenyl ether) and by-products (hexachlorobenzene; polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans [PCDD ⁄PCDF], PCB, alpha hexachlorocyclohexane, beta hexachlorocyclohexane and pentachlorobenzene). (Source: http://chm.pops.int/Convention/tabid/54/ language/en-US/Default.aspx). An epidemiologist at Kyung-pook National University College of Medicine, Korea, Duk-Hee Lee, found some years ago that serum levels of gamma glutaryl transferase (GGT) within its reference range strongly predicted the future risk of diabetes in a cohort study in Korea. After confirming this association in other well-established cohort studies, she asked herself why this relationship should exist. She hypothesized that this association might be a result of exposure to some environmental pollutants, as GGT is an enzyme that is involved in the metabolism of glutathione, and glutathione is known as a detoxification agent. After a review of literature on environmental pollutants, she became convinced that POP might be responsible. To prove the association between POP and diabetes ⁄metabolic syndrome in humans, POP should be measured. However, measuring POP levels is very difficult, prohibitively expensive and needs a devoted machine (usually GC ⁄MS), facilities and people. Luckily for her, she found that the US Center for Disease Control and Prevention, already had measured the 50 most frequently detected POP in blood samples taken during the US 1999–2002 National Health and Nutrition Examination Survey (NHANES) for biomonitoring POP in the USA general population. NHANES is designed to be nationally representative of the non-institutionalized USA civilian population on the basis of a complex multistage probability sample. The majority of participants were found to have serum concentrations under the limit of detection (LOD) of many kinds of POP. Therefore, they selected six POP (2,2,4,4,5,5-hexachlorobiphenyl [PCB153], 1,2,3,4,6,7,8-heptachlorodibenzo-p-dioxin [HpCDD], 1,2,3,4,6,7,8,9octachlorodibenzo-p-dioxin [OCDD], oxychlordane, p,p-dichlorodiphenyltrichloroethane [DDE], and trans-nonachlor) for which at least 80% of the study subjects had concentrations more than the LOD. The results were striking. A body load of persistent organic pollutants (as a matter of fact, a sum of six POP) was associated with the prevalence of diabetes in a strong dose-dependent manner (Figure 1). The association was stronger among obese subjects than non-obese patients. Furthermore, it was striking to see when POP concentrations were very low, the prevalence of diabetes was very rare among the obese subjects with BMI ‡ 30 kg ⁄m. Further analysis of NHANES data showed POP levels were also associated with several other conditions, including metabolic syndrome. Observations showing the association between POP and diabetes soon followed from Denmark (Greenland Inuit), Taiwan, Japan, and very recently from the Slovak Republic. These data appear too strong to deny a causal association. However, the mere presence of a statistical association between two variables, POP and diabetes ⁄metabolic syndrome in our case, does not establish a cause–effect relationship. Does exposure to POP induce insulin resistance? Soo Lim et al. at Seoul National University Medical College, Korea, reported that rats treated with low doses of atrazine develop insulin resistance along with EDITORIAL