The Pine River Statement: Human Health Consequences of DDT Use

1Dichlorodiphenyltrichloroethane (DDT) is a potent insecticide that was used worldwide for agricultural and public health purposes from the 1940s until the 1970s, when concern about its toxic effects on wildlife and humans, its environmental persistence, and its concentration in the food supply led to restrictions and prohibitions on its use. Commercial mixtures, often called technical-grade DDT, contain two major isomers, the active ingredient, p,p′-DDT, and a by-product, o,p′-DDT. DDT and its primary breakdown product, dichlorodiphenyldichloro-ethylene (DDE), are highly lipophilic, persist in the environment, and bioaccumulate in humans because of their long half-lives (6 years and possibly up to 10 years, respectively).

2DDT was identified as a potent insecticide in 1939 and was heavily used during World War II. After the war, DDT became the global insecticide of choice in households, for agriculture, and for public health vector-control projects. In 1962, Rachel Carson, in Silent Spring, noted that DDT bioaccumulates and biomagnifies up the food chain and raised concerns that the pesticide may have long-lasting effects on wildlife and possibly on humans.

3In the United States, all nonpublic health uses of DDT were banned by 1972. Regulation by some other nations occurred more gradually. DDT continues to be used for malaria control in several African and Asian countries. In 2001, more than 100 countries signed the Stockholm Convention on Persistent Organic Pollutants (POPs), committing to eliminate the use of 12 POPs of greatest concern to the health of the global community, including DDT. By 2008, 160 countries had ratified the Stockholm Convention, making it one of the most successful inter national environmental agreements. Recognizing the continued need for DDT use in some countries, the convention allows the production and use of DDT for disease vector control only, provided that no safe, effective, and affordable alternatives are locally available. In these cases, the convention requires parties to notify the convention secretariat of their intention to produce and/ or use DDT for vector control and to prevent or minimize human exposure and release into the environment. In 2006, the World Health Organization (WHO) and the U.S. Agency for International Development (USAID) endorsed indoor DDT spraying to control malaria.

4On 14 March 2008, researchers met for the Eugene Kenaga International DDT Conference, which was jointly organized by the Pine River Superfund Citizen Task Force, the Center for Responsible Leadership, and the Public Affairs Institute of Alma College with the endorsement of the International Society of Environmental Epidemiology, the Society for Environmental Toxicology and Chemistry, Alma College, and the Pine River Superfund Task Force. The goal of the conference was to bring together experts on DDT and concerned citizens to address the current and legacy implications of DDT production and use. This conference was held at Alma College, near the Velsicol Chemical Corporation U.S. Superfund site in Gratiot County, Michigan.

5The purpose of this review is to summarize information on health risks so as to better inform risk–benefit analyses and policy. We do so by reviewing evidence of human exposure to DDT and some of its potential health consequences, focusing primarily on studies that have been published since the endorsement of DDT by WHO and USAID and since the publication of other literature reviews on the subject. We conducted a search of PubMed (National Library of Medicine, Bethesda, MD, USA) to find human studies (excluding case reports) published in English from 2003 to 2008 by using the following search terms: (DDT OR DDE) AND (toxicity OR health OR cancer OR carcinogenicity OR reproduction OR estrogen OR neurological OR development OR exposure OR diabetes OR pregnancy OR miscarriage OR spontaneous abortion OR birth weight OR gestation OR lactation OR birth defects OR growth OR puberty OR fertility OR neurotoxicity OR neurodevelopment OR immunological). We identified 494 papers and reviewed them for primary research. On the basis of available data, we make recommendations regarding the introduction, continuation, or reintroduction of DDT use worldwide. These recommendations represent the consensus opinion of the authors and participants present at the Eugene Kenaga International DDT Conference.

6Environmental and biological monitoring studies in the United States demonstrate that use restrictions were successful in lowering human exposure to DDT. Estimated dietary intake of DDT dropped > 200% between 1970 and 1986, whereas serum DDT concentrations declined 9-fold between 1980 and 2000. Recent studies in the United States report low concentrations of DDT and DDE in food and in house dust and soil. Yet nearly all U.S. residents have measurable serum p,p′-DDE levels, whereas p,p′-DDT is detected in 5–10% of the population.

7A sample of recent studies of DDT/DDE serum levels in pregnant women and women of reproductive age shows the different exposure scenarios around the world. In this sample of studies, low concentrations were observed in U.S. women of reproductive age participating in the 2001–2002 wave of the National Health and Nutrition Examination Survey (NHANES; Table 1). The median DDE serum concentration was 10-fold higher in a population of primarily Mexican immigrant women living in an agricultural area of California where half of the women had immigrated within the previous 5 years. DDE concentrations in this Mexican-American cohort were similar to those of a concurrent population living in Morelos, Mexico, where DDT probably had not been used for some time. However, median DDE serum concentrations in women residing in Chiapas, Mexico, where DDT may have been used up until 2000, were about five times higher in 1998 than in Morelos and within the range observed in older studies from the United States when DDT was still being used. However, the concentrations in pregnant women in Chiapas are still orders of magnitude lower than those reported in a study of South African men whose houses were sprayed with DDT as part of indoor residual spraying programs (mean blood DDE concentration = 239 ± 215 μg/g lipid). Other studies conducted in South Africa also reported very high levels of DDT/DDE in breast milk. It may be that the pattern of use and/or formulation of DDT for malaria control differed in Chiapas and South Africa. Nevertheless, these data suggest that indoor residual spraying results in high DDT exposure in humans, including vulnerable populations, such as pregnant women and fetuses.

8In 1991, the International Agency for Research on Cancer (IARC) rated DDT as “possibly carcinogenic to humans (Group 2B)”. This rating was largely based on the induction of liver tumors in experimental animal studies that reported significant increases in hepatomas (neoplastic liver cell tumors) in multiple strains of male and female rodents exposed to technical DDT orally (gav-age or diet) or to p,p′-DDE (diet). Most human studies reviewed by IARC in 1991 did not show an association between DDT exposure and cancer risk. Some studies suggested that DDT exposure may be associated with certain cancers (lung cancer and lymphomas); however, the lack of control for exposure to other chemicals, small study size, insufficient data on confounding factors (e.g., incomplete information on tobacco use), and short follow-up time for long-latency cancers limited the ability to make any conclusions at that time. Research on DDT/DDE exposure and cancer continued to yield mixed results after the publication of the IARC report. We review the recent research with a focus on cancers of the liver, pancreas, and breast.

9In an ecologic study, found that standardized mortality rates (SMRs) for liver cancer were elevated in whites but not in African Americans who lived in states with high population-level adipose tissue DDE concentrations. These researchers offered no explanation for this racial difference. In a case–control study, reported that the risk of liver cancer was significantly elevated in Chinese men with the highest blood levels of DDT [odds ratio (OR) = 3.8; 95% confidence interval (CI), 1.7–8.0] compared with men with lower levels of DDT. Blood levels of DDE were not associated with a higher risk.

10Mechanistic data suggest that DDT could play a role in pancreatic cancer by modulating activation of the oncogene K-ras. An association of workplace exposure to DDT and the risk of pancreatic cancer is supported by two studies. In a cohort of 5,886 DDT manufacturing plant workers, reported a 7.4-fold higher risk of pancreatic cancer deaths in workers exposed to DDT for an average of 47 months, as determined using work records and interviews with coworkers, compared with workers who had no exposure. Similarly, deaths from pancreatic cancer were significantly higher in a cohort occupationally exposed to DDT compared with a control cohort in an Australian study with follow-up data from 1935 to the 1990s (SMR = 3.57; 95% CI, 1.09–15.40). In contrast, other studies have found no association between estimates of DDT exposure among workers or serum/ adipose tissue levels of p,p′-DDE and pancreatic cancer risk after adjustment for confounders. It has been suggested that the etiology of pancreatic cancer may be causally linked to diabetes mellitus and hyperinsulinemia and thus linked to associations between DDT and diabetes (see below).

11Although neither DDT nor DDE induced mammary tumors in laboratory animal cancer bioassays, early studies suggested that DDE levels in women were associated with a higher risk of breast cancer. Two recent case–control studies also showed higher DDE blood concentrations in cases than controls. However, most case–control studies recently published and reviewed have not supported an association.

12The literature on DDT and breast cancer has two main limitations. First, most studies used biological samples collected well after exposure to technical DDT had occurred and relied on serum concentrations of p,p′-DDE as a proxy for exposure to “DDT.” Second, most studies included women who would not have been exposed to technical DDT when young, yet both animal and human studies of radiation exposure strongly suggest that the breast is most vulnerable to environmentally induced carcinogenesis during several critical periods such as in utero, before menarche, and before first pregnancy.

13Overcoming these past limitations, measured concentrations in archived serum samples collected between 1959 and 1967 (peak years of DDT use) from pregnant women participating in the Child Health and Development Studies (CHDS). Medical records were obtained nearly 40 years later. Among women who were = 14 years of age by 1945 (when DDT was first introduced for use by the general public), those with blood concentrations in the highest tertile were five times more likely to develop breast cancer than those with blood levels in the lowest tertile (OR = 5.4; 95% CI, 1.7–17.1). However, there was no association between serum p,p′-DDT levels and adult risk of breast cancer among women who were not exposed before 14 years of age, and interaction by age in 1945 was statistically significant. This study suggests that the prepubertal and pubertal years are critical periods of exposure. Thus, previous studies that measured exposure in older women may have missed the critical period.

14Research has not supported an association of DDT or DDE and incidence of colorectal, lung, bladder, prostate, endometrial, and stomach cancers. Although no associations were found with serum DDT, higher DDE levels in dust, adipose tissue, and plasma have been associated with non-Hodgkin lymphoma in case–control studies. For other cancers, such as leukemia, and testicular cancer, evidence remains equivocal.

15Since initial observation that the sum of DDT and DDE levels in serum was 29% higher in occupationally exposed workers with diabetes compared with nondiabetics, a number of other studies have been published on this subject. For example, data from the 1999–2002 NHANES suggested that elevated serum concentrations of p,p′-DDT and p,p- ′ DDE were significantly associated with the prevalence of diabetes. In addition, reported an increasing trend in the odds of diabetes as exposure to p,p′-DDE increased (ptrend < 0.001) with an OR of 4.3 (95% CI, 1.8–10.2) for those = 90th percentile of exposure compared with those in the lowest quartile.

16Because diabetes occurs in Mexican Americans twice as frequently as in non- Hispanic whites, and serum levels of p,p′-DDE and p,p′-DDT are higher in Mexican Americans than other ethnic groups in the U.S. population, data from the Hispanic Health and Nutrition Examination Survey (HHANES) for 1982–1984 were analyzed. Serum p,p′-DDT or p,p′-DDE levels were dose related to the prevalence of self-reported diabetes in Mexican Americans. Additionally, in a study of Native Americans (Mohawks), observed a significant positive association between diabetes prevalence and serum levels of p,p′-DDE.

17A Swedish study found that diabetes prevalence was significantly higher (ptrend = 0.04) in Baltic Sea fishermen with elevated serum DDE levels, but not in their wives. With a larger study population (non-fisherman families), the same authors reported a significant positive association (ptrend < 0.01) between type 2 diabetes and serum p,p′-DDE levels in Swedish women.

18Collectively, these studies from the United States and Sweden suggest that body burdens of DDT and/or DDE may be associated with the prevalence of diabetes. A variety of other persistent environmental chemicals also have been associated with diabetes prevalence. However, given the high correlation among various organochlorine exposures, additional research is needed to delineate the specific contributions of DDT and DDE.

19In the U.S. Collaborative Perinatal Project (CPP), where the median maternal serum DDE level was 24.5 μg/L, high DDE concentrations (45–59 vs. < 15 μg/L) were associated with an increased risk of fetal loss in previous pregnancies. Although the outcome occurred before DDE measurement, this study of 1,717 women corroborated findings from smaller studies. studied 338 nulliparous Chinese textile workers with similar DDE concentrations (median, 29 ng/g serum) for the risk of early pregnancy loss (measured by daily human chorionic gonadotropin). Authors reported an OR of 1.17 (95% CI, 1.05–1.29) for each 10-ng/g serum increase in total DDT. In a case– control study of habitual aborters, researchers did not observe higher mean serum DDE levels in cases relative to controls.

20Early studies on DDE and preterm delivery (< 37 weeks of gestation) were small, and results were inconsistent. Studies using data from larger cohorts also have not consistently supported an association between exposure to DDT/DDE and birth weight or gestational duration. In a study of 2,380 pregnant women participating in the CPP, found that the odds of preterm delivery were 3.1 times higher (95% CI, 1.8–5.4) in women with serum DDE = 60 μg/L compared with those with DDE < 15 μg/L during pregnancy. Adjusted odds of having a child small for gestational age also increased, but less consistently (ptrend = 0.04). However, two analyses of the CHDS, which was conducted around the same time as the CPP, have found no associations of DDT/DDE and preterm delivery or small for gestational age, despite slightly higher median DDE levels than in the CPP (43 vs. 25 μg/L).

21Most studies of more recent cohorts, which had somewhat lower exposure than those in the earlier studies, did not find an association between maternal serum measurements of DDE and/or DDT and gestational duration, premature labor, birth weight, or other measures of fetal growth such as crown–heel length or head circumference, although some studies did find associations. The high DDE serum concentrations observed in the CPP and CHDS cohorts during the 1960s are several-fold higher than current serum levels, but substantially lower than in populations where indoor residual spraying is occurring.

22Two studies have found a shorter duration of lactation among mothers with high breast milk DDE concentrations. A North Carolina study of 858 women indicated that higher breast milk DDE concentrations were associated with a shorter median duration of lactation (2.5 months for DDE > 6 μg/g lipids vs. 6.5 months for DDE < 1 μg/g lipids). A study of 229 Mexican women found similar results, but only among women who had previously lactated. Estrogenic effects of DDT were postulated to affect prolactin levels and milk production. A more recent study suggested that DDE serum concentrations were related to decreased rates of breast-feeding initiation as well as shortened duration of lactation in women who had never breast-fed and in non-smoking women, but a Mexican study found that serum DDE was associated with duration of lactation only in women who previously breast-fed. In this Mexican study of 784 mothers of male term babies, the hazard ratio of weaning for women with high serum DDE levels (cutoff point, 9 μg/g lipids) was 1.76 (95% CI, 1.22–2.53) in women who had previously breast-fed and 0.91 (95% CI, 0.66–1.26) in women who had never breast-fed. Previous lactation can reduce the maternal body burden of DDE, and women who breast-feed longer for previous infants tend to do so for the current baby. Thus, associations between DDE levels and early weaning may be spurious, and further research is warranted.

23Studies in rats have suggested a relationship between fetal tissue concentrations of 10–20 ppm of p,p′-DDE and reproductive abnormalities in male offspring. In the CPP birth cohort, reported ORs of 1.07 (95% CI, 0.97–1.18) for cryptorchidism (n = 219), 1.01 (95% CI, 0.90–1.14) for hypospadias (n = 199), and 1.06 (95% CI, 0.97–1.16) for polythelia (n = 167) for each 2.67 μg/g lipid increase in maternal serum p,p′-DDE. However, in the CHDS birth cohort, found that the odds of cryptorchidism were twice as high in participants with p,p′-DDT levels above versus below the median (OR = 1.97; 95% CI, 1.40–2.54) but found no associations between maternal serum p,p′-DDE and the odds of cryptorchidism, or between p,p′-DDT and p,p′-DDE concentrations and odds of hypospadias. A Spanish study also reported more than a doubling of the odds of cryptorchidism and/or hypospadias cases associated with detectable levels of p,p- ′ DDT (OR = 2.63; 95% CI, 1.21–5.72) and o,p′-DDT (OR = 2.25; 95% CI, 1.03–4.89) measured in placental tissues. Other studies conducted in France and in Finland and Denmark reported increased colostrum levels of p,p′-DDE, and elevated breast milk concentrations of p,p′-DDT, o,p′-DDT, p,p′-DDE, and p,p′-dichloro-diphenyldichloroethane (DDD), respectively, in cases of cryptorchidism compared with controls, although associations were not statistically significant.

24Evidence for an association between physical growth after birth and DDT and DDE exposure is inconsistent. Maternal DDT concentrations were not associated with child weight or height at 5 years of age in children participating in the CHDS. In contrast, those who had the highest prenatal concentrations of DDE in the CPP cohort (= 60 μg/L) compared with the lowest (< 15 μg/L) were significantly shorter at 1, 4, and 7 years of age. However, a study that examined growth in adolescent boys participating in the CPP found no relation between maternal serum levels of DDE or DDT in pregnancy and height, body mass index (BMI), and other measures of growth. Two other studies in older children and in populations with much lower serum levels reported conflicting findings: A study from Germany found shorter height in 8-year-old girls in relation to higher DDE concentration, and an older North Carolina study found a relation to taller height in boys 12–14 years of age. Overall, the evidence for the relation of maternal DDT exposure and child physical growth is weak.

25A small number of human studies have examined DDT/DDE and onset of menarche in girls, with two studies finding associations of earlier age at menarche with higher exposure and one study finding no association. found that women with higher serum levels of total DDT (i.e., the sum of p,p′- and o,p′-isomers of DDT, DDE, and DDD) measured in adulthood (mean age, 24.9 years) reported significantly earlier age at onset of menarche, adjusting for BMI and birth year. In contrast, found no association between concurrent DDE blood concentrations [geometric mean (GM) = 0.35 ppb] and menarcheal status among 138 Mohawk girls 10–16.9 years of age. estimated serum DDE levels during pregnancy in 151 women by back-calculating from measurements made up to 25 years later. They reported that higher (estimated) prenatal DDE levels were associated with earlier age at menarche in daughters (adjusted β = −0.07, p = 0.04).

26Two studies examined onset of puberty rather than menarche in relation to DDE exposure. found no association between transplacental or lactational DDE concentrations and pubertal stage as self-reported in a cohort of approximately 315 adolescent girls with relatively high exposure (range, 0.3–25.8 ppm). performed Tanner exams on approximately 80 9-year-old girls and found no difference in concurrent DDE plasma levels in those girls who had reached Tanner breast stage 2 (onset of puberty) and those who did not, but DDE levels were low. Only one study has examined onset of puberty in boys. found no association between DDE and self-reported Tanner staging in boys up to 16 years of age. All these studies examined associations with DDE and not DDT.

27Although these studies of puberty and menarche suggest an association with exposure, no study has examined the relationship of serum levels of DDE and DDT concentrations in blood collected before puberty in relation to Tanner staging in girls or boys.

28Researchers have investigated the seminal parameters of men living in regions of high DDT use. In one such study, participants were drawn from rural communities in the malaria-endemic region of Chiapas, Mexico, with a history of high use and where DDT was sprayed inside their homes at least annually from the late 1940s until 1997; sampling took place between 2000 and 2001. The mean serum DDE concentration (45 ± 31 μg/g lipids) was 100 times higher than reported in unexposed populations. The percentage of motile sperm was negatively correlated with plasma DDE concentrations, whereas the percentage of sperm with morphologic tail defects and insufficient sperm chromatin condensation was positively correlated with these levels.

29In a study conducted in Limpopo, South Africa, men were selected from rural communities in a malaria-endemic area where DDT is sprayed annually inside unpainted houses, but not inside painted houses. The GM serum concentrations of DDT (90.2 ± 102.4 μg/g) and DDE (215.5 ± 210.6 μg/g) in the 311 participants from this area were extremely high. DDT and DDE serum concentrations were also significantly higher (p < 0.001) in participants whose houses were sprayed with DDT (101.9 μg/g lipid DDT and 239.0 μg/g lipid DDE) compared with those whose houses were not sprayed (30.5 μg/g lipid DDT and 99.5 μg/g lipid DDE). Their semen volume was low (1.9 ± 1.3 mL) and several sperm motion parameters were impaired, including the percentage of motile sperm in men with higher DDT (r = −0.27, p < 0.001) and DDE concentrations (r = −0.20, p < 0.001). In another cross-sectional study of 48 DDT applicators conducted in Limpopo, overall semen quality was low, and DDT, but not DDE, serum levels were associated with decreased sperm count.

30Studies of semen quality or genetic markers in sperm have been conducted in other populations, usually with lower exposure than noted in Chiapas or South Africa. For example, case–control studies of men of sub-fertile couples have found no difference in the men’s DDE serum levels but higher current blood levels in the mothers of the cases compared with controls, and no association with DNA integrity (neutral comet assay). Similarly, the multinational (Greenland; Warsaw, Poland; Kharkiv, Ukraine; and Sweden) INUENDO study of European and Inuit pregnant women and their spouses failed to find associations of DDE serum levels and conventional measures of semen quality, chromatin integrity, and hormone levels or a measure of apoptosis. However, as in many populations where exposure to several organochlorines, including polychlorinated biphenyls, may be highly correlated, independent associations with DDE often could not be established.

31Overall, studies of highly exposed populations suggest that male fertility may be adversely affected by DDT exposure, but studies in populations with moderate to low exposure levels do not support a relationship between exposure and male fertility outcomes.

32Two recent studies examined the relationship of DDT/DDE levels and menstrual cycle characteristics and found only weak associations. However, one study from the INUENDO population reported a 3-fold increase in risk of long menstrual cycles among Polish women but not among women from other European countries. Another study using data from the Hispanic Health and Nutrition Examination Survey found that both DDT and DDE levels were associated with a significantly earlier age of menopause.

33Two cross-sectional studies found suggestive evidence that p,p′-DDE serum levels in pregnant women were correlated with delays in conception, but another study in Mexican-American women did not find a relation with either p,p′-DDT or p,p′-DDE serum levels. One of these studies also examined paternal serum p,p′-DDE and found no effects on partners’ time to pregnancy. In contrast, a study of 105 male DDT applicators found that p,p′-DDE exposure, estimated by occupation history, was associated with delayed time to pregnancy in their spouses, defined using marriage dates and birth dates of first-born children.

34The only study to examine in utero exposure to DDT and time to pregnancy was conducted among 289 women born in California between 1960 and 1963 (CHDS). Authors found that each 10-μg/L increase in mothers’ serum concentrations of p,p′-DDT and p,p′-DDE during pregnancy was associated with a 32% reduction and a 16% increase, respectively, in their daughters’ per cycle probability of pregnancy. The ratio of these two compounds varied considerably, and longer time to pregnancy in daughters was observed as the ratio of p,p′-DDT to p,p′-DDE increased in maternal serum samples. Findings suggest that recent exposure or direct exposure to the pesticide, rather than chronic exposure to p,p′-DDE in the food chain, was the underlying risk factor.

35Overall, the few studies conducted to date suggest that DDT exposure may affect time to pregnancy, but more research is needed.

36DDT exerts its insecticidal effects by disrupting the nervous system. Animal studies confirm that DDT is a neurodevelopmental toxicant. In mice, exposure to DDT timed to sensitive periods of pre-natal and neonatal nervous system development has been shown to cause behavioral and neurochemical changes into adulthood.

37The few studies conducted in humans have focused primarily on exposure to DDE rather than DDT. In a North Carolina birth cohort recruited in the 1980s, reported that maternal serum and breast milk DDE levels were related to hyporeflexia in a dose-dependent fashion in infants assessed by the Brazelton Neonatal Behavioral Assessment Scale (BNBAS), but this finding has not been replicated in more recent studies. In a recent investigation from Massachusetts, DDE measured in cord blood was negatively related to BNBAS measures of alertness and attention and positively related to measures of irritability, although only the trend for irritability was significant.

38The North Carolina study reported no adverse association between perinatal DDE exposure and performance on the Bayley Scales of Infant Development (BSID) from 6 to 24 months of age; on the McCarthy Scales of Children’s Abilities (MCSA) at ages 3, 4, and 5 years; or on school performance at 8–10.5 years. Similarly, a study conducted in Oswego, New York, found no association of DDE levels and performance on the Fagan Test of Infant Intelligence at 6 and 12 months of age. However, a smaller Spanish study of 92 infants 13 months of age found a significant negative association between relatively low cord serum DDE levels and cognitive, psychomotor, and social development on the BSID and Griffith Scales of Infant Development. Similarly, a study of 230 infants from Mexico found that maternal serum DDE levels were inversely associated with psychomotor development scores on the BSID at 3, 6, and 12 months. Using the Center for the Health Assessment of Mothers and Children of Salinas (CHAMACOS) cohort of Mexican-American children, also reported an inverse association of maternal serum DDE and psychomotor development at 6 and 12 but not at 24 months, and with mental development at 24 months.

39In a small study measuring visual evoked potentials (VEPs) in 12-month-olds, wave latency VEPs at 15 min were significantly related to the colostral levels of both DDT and DDE, and wave latency VEPs at 60 min were related to levels of DDT. However, findings were no longer statistically significant after authors controlled for the plasma levels of long-chain polyunsaturated fatty acids, thought to be one of the beneficial components of breast milk for brain development. The authors concluded that breast-feeding in itself may exert a protective effect against contaminants in human milk.

40Only two studies have examined the relationship of DDT levels and cognitive functioning. Increased maternal serum DDT levels were associated with poorer psychomotor development at 6, 12, and 24 months and mental development at 12 and 24 months in the CHAMACOS cohort. Breast-feeding did not have a negative relationship with mental development in the group with the highest maternal DDT levels. In another study, cord serum DDT levels were also found to be associated with poorer performance in general cognitive, memory, quantitative, verbal, and executive function domains of the MCSA in 4- and 5-year-old children in Spain.

41These studies suggest that DDT, and less so DDE, may be associated with neurodevelopmental deficits. In addition, breast-feeding may modulate some of the negative effects of DDT, but this needs to be examined when exposure is high such as in communities where indoor residual spraying is occurring. Follow-up studies of these populations are needed to verify whether these developmental deficits persist.

42Although thyroid hormones are essential for normal brain development, studies suggest that DDE, and possibly DDT, may depress triiodothyronine (T3) and/or thyroxine (T4) in maternal, cord, and preschool children’s blood but not entirely consistently. Higher DDT levels were also found in cases of congenital hypothyroidism relative to controls. Results from studies conducted in men and nonpregnant women have generally been inconsistent. Two of these studies reported a positive association between serum DDE and thyroid-stimulating hormone (TSH) concentrations, one found a positive correlation between DDE and total T3, whereas other studies found no associations between DDE and TSH, total T3 or the free T4 index.

43DDT and particularly DDE have demonstrated the potential for modulating the human immune response as measured by multiple markers such as interleukin-4 and interleukin-13, plasma levels of type 1 (interferon-γ) response to mitogen in nursing mothers, white blood cell counts, and various lymphocyte phenotypes, and immunoglobulin (Ig) A, G, and E levels. Associations with immune system–related conditions such as aplastic anemia (with DDT but not DDE), asthma (with DDE), otitis media (with DDE), and farmer’s lung (with technical DDT use) were also reported. In children, one cross- sectional study of German schoolchildren found that DDE levels in blood were associated with increased IgE blood levels and asthma. A longitudinal study of 405 Spanish children confirmed the association between DDE exposure and asthma, but found that DDE was not associated with IgE levels. Additional research is needed to understand the effects of DDT/ DDE on the immune system and associated diseases, especially because DDT is used in areas where there are often high rates of HIV.

44The use of DDT historically may have helped prevent millions of infections and deaths from insect-borne diseases. Based on recent studies, we conclude that humans are exposed to DDT and DDE, that indoor residual spraying can result in substantial exposure, and that DDT may pose a risk for human populations. However, few studies have measured body burdens of both DDE and DDT, and studies have rarely investigated the effects of DDT/DDE exposure at levels observed in populations exposed through indoor residual spraying. Furthermore, information on exposure to DDT/DDE during critical periods is limited for outcomes such as cancer.

45We are concerned about the health of children and adults given the persistence of DDT and its active metabolites in the environment and in the body, and we are particularly concerned about the potential effects of continued DDT use on future generations. We recognize the serious implications of restricting DDT use given that an estimated 880,000 people die each year from malaria, most of whom are < 5 years of age. Given our continually deepening understanding of the effects of DDT use on humans, we ask global policy makers to consider the following issues:

46In the United States, individuals have been exposed to DDT by working in occupational settings and by living in proximity to DDT manufacturing facilities. State and federal agencies should monitor levels of contaminants in residents near Superfund sites (e.g., Pine River/Velsicol Chemical Corp. Michigan Superfund site) and conduct health effects studies if biomonitoring indicates persistently elevated levels of DDT or DDE.

47Few studies of health outcomes have been conducted in populations where indoor residual spraying with DDT is occurring. These populations likely have much higher exposures to DDT and may differ from those previously studied in ways that might affect susceptibility (e.g., genetics, diet, health status, and social class). Research is needed to determine the exposure and health risks associated with DDT used for indoor residual spraying in the relevant communities.

48Children, pregnant women, and those who are immunocompromised may be most at risk for the effects of DDT. People in many malaria-endemic areas where DDT is being used also have high rates of HIV/AIDS infection.

49Breast-feeding is the best form of nutrition for infants and is recommended up to at least 1 year of age by the. In some African countries, women may breast-feed for up to 2 years. However, because of the lipophilic nature of DDT/DDE, breast milk is a major route of DDT/DDE exposure to infants. Significant public health consequences could ensue should breast-feeding be discouraged as a result of high DDT contamination.

50DDT may be a valuable short-term approach for controlling malaria, but measures should be taken to reduce human exposure to this pesticide. DDT exposure could conceivably be reduced through strict adherence to indoor residual spraying guidelines, better education of communities and applicators regarding the potential hazards of DDT exposure, improved application methods and formulations, and a better understanding of the determinants of exposure.

51New methods of vector control should be developed and rigorously tested considering local differences such as in vectors, parasites, ecology, and culture. As is the case for DDT, new methods for vector control should be evaluated not only for their effectiveness, but also for their potential adverse effects on the environment and populations, including to susceptible subpopulations such as those who are immunocompromised and malnourished. For example, pyrethroids have been substituted for DDT in indoor residual spraying in some locations, yet there is little information on their effects to human health.

52Current evidence on DDT exposure to human populations and on its potential health effects support the Stockholm Convention on Persistent Organic Pollutants, which emphasizes that DDT should be used with caution, only when needed, and when no other effective, safe, and affordable alternatives are locally available. Under the convention, each country currently using DDT is required to provide an implementation and management plan to limit the use of DDT to disease vector control and to reduce reliance on DDT. Countries should be assisted so that they can ultimately rely on other sustainable methods, techniques, and strategies for malaria control. Given the paucity of data in populations who are currently potentially exposed to high levels of DDT, we urge the global community to monitor exposure to DDT and to evaluate its potential health impacts both in malaria-endemic regions of the world and in locations where DDT use has been historically high, such as the Pine River Superfund site.