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| Critical Windows of Exposure to Household Pesticides and Risk of Childhood Leukemia Xiaomei Ma,1 Patricia A. Buffler,1 Robert B. Gunier,2 Gary Dahl,3 Martyn T. Smith,1 Kyndaron Reinier,1 and Peggy Reynolds2 1School of Public Health, University of California, Berkeley, California, USA; 2Environmental Health Investigations Branch, California Department of Health Services, Oakland, California, USA; 3Stanford University School of Medicine, Stanford, California, USA Abstract The potential etiologic role of household pesticide exposures was examined in the Northern California Childhood Leukemia Study. A total of 162 patients (0-14 years old) with newly diagnosed leukemia were rapidly ascertained during 1995-1999, and 162 matched control subjects were randomly selected from the birth registry. The use of professional pest control services at any time from 1 year before birth to 3 years after was associated with a significantly increased risk of childhood leukemia [odds ratio (OR) = 2.8 ; 95% confidence interval (CI) , 1.4-5.7], and the exposure during year 2 was associated with the highest risk (OR = 3.6 ; 95% CI, 1.6-8.3) . The ORs for exposure to insecticides during the 3 months before pregnancy, pregnancy, and years 1, 2, and 3 were 1.8 (95% CI, 1.1-3.1) , 2.1 (95% CI, 1.3-3.5) , 1.7 (95% CI, 1.0-2.9) , 1.6 (95% CI, 1.0-2.7) , and 1.2 (95% CI, 0.7-2.1) , respectively. Insecticide exposures early in life appear to be more significant than later exposures, and the highest risk was observed for exposure during pregnancy. Additionally, more frequent exposure to insecticides was associated with a higher risk. In contrast to insecticides, the association between herbicides and leukemia was weak and nonsignificant. Pesticides were also grouped based on where they were applied. Exposure to indoor pesticides was associated with an increased risk, whereas no significant association was observed for exposure to outdoor pesticides. The findings suggest that exposure to household pesticides is associated with an elevated risk of childhood leukemia and further indicate the importance of the timing and location of exposure. Key words: case-control studies, child, herbicides, insecticides, leukemia, pesticides. Environ Health Perspect 110:955-960 (2002) . [Online 14 August 2002] http://ehpnet1.niehs.nih.gov/docs/2002/110p955-960ma/ abstract.html Address correspondence to X. Ma, School of Public Health, University of California, Berkeley, CA 94720-7360 USA. Telephone: (510) 643-3958. Fax: (510) 643-1735. E-mail: xmma@uclink4.berkeley.edu We thank J. Feusner, K. Matthay, S. Month, V. Crouse, K. Leung, and V. Kiley for assistance with recruiting patients and M. Does for supervising fieldwork. The study was supported by grants from the National Institute of Environmental Health Sciences (PS42 ES04705 and RO1 ES09137) . X.M. was supported by a grant from the Centers for Disease Control and Prevention (T01/CCT917644-01) . Received 14 November 2001 ; accepted 12 March 2002. |
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Most studies evaluating the relationship between household pesticide exposures and childhood leukemia suggest that an increased risk of leukemia is associated with in utero and postnatal pesticide exposures ( 1,2). Nevertheless, previous studies have a number of limitations. Some of the estimated odds ratios (ORs) are not precise; that is, they have wide confidence intervals ( 3-5). Some studies have relatively low response rates ( 5-7) or are based on small numbers of cases ( 3,4,6,8,9). In addition, several study design issues could have contributed to problems in recall and reporting of household pesticide exposures, including source and recruitment of controls, matching criteria, method and timing of data collection, imprecise time intervals for which exposure data were collected, definition of exposure, and use of surrogate respondents. Because of the uncertainties in existing data, there is a compelling need to evaluate further the relationship between pesticide exposures and childhood leukemia, and to do so in studies with improved exposure classification and reduced differential reporting.
Study population. During the first phase (1995-1999) of the Northern California Childhood Leukemia Study (NCCLS), patients (0-14 years old) with newly diagnosed leukemia were rapidly ascertained from major clinical centers, usually within 24 hr after diagnosis. Although case ascertainment was hospital based, we compared the cases with those ascertained by the statewide population-based registry ( 10) and found that the NCCLS protocol successfully identified 88% of all newly diagnosed childhood leukemia cases in the San Francisco-Oakland metropolitan statistical area. Controls were randomly selected from the statewide birth certificate files maintained by the California Department of Health Services (Sacramento, CA) and 1:1 matched to cases on date of birth, sex, mother's race (white, black, or other), Hispanicity (either parent is Hispanic), and mother's county of residence at the time of child's birth. These controls were then traced by using commercially available searching tools. For cases not born in California (< 10% of all cases), county of residence at diagnosis was used for the matching. For each case, the search continued until an eligible control subject consented to participate in the study.
To be eligible, each case or control had to reside in the study area, be under 15 years of age at the time of diagnosis (or corresponding date for the control), have at least one parent or guardian who speaks English or Spanish, and have no previous history of any malignancy. Approximately 83% of the eligible cases consented to participate. Among all the eligible controls approached, 69% consented to participate. The study protocol was approved by the Institutional Review Boards of all collaborating institutions, and written informed consents were obtained for all participating subjects. A total of 162 matched case-control pairs are included in this analysis. Of the 162 patients, 135 had a diagnosis of acute lymphoblastic leukemia (ALL).
Data collection. In the NCCLS, detailed information on household pesticide use, including the name of each product, intended purpose (e.g., cockroach control), frequency of use, and time window of use (3 months before pregnancy, pregnancy, and years 1, 2, and 3), was collected through in-home personal interviews with the primary care giver, usually the biologic mother, shortly after diagnosis (corresponding dates for controls). For cases, the mean interval between diagnosis and in-home interview was 4.8 months. Because potential birth certificate controls needed to be identified from the birth registry and traced, the interview of a case usually preceded the interview of the corresponding control, with a mean lag time of 9.5 months.
Different types of pesticides were grouped for analysis. Unless the use of professional services was explicitly stated, all products were assumed to be personally applied. As defined in this article, insecticide exposures include professional pest control services, insect repellents, and the use of various products to control ants, flies, cockroaches, spiders, termites, and plant/tree insects; herbicide exposures include professional lawn service and the use of weed control products; flea control products include indoor foggers, flea collars, flea soaps or shampoos, and sprays, dusts, or powders for fleas. The use of flea control products is directly related to the presence of cats and/or dogs in the households, and the percentage of households in which the child had regular contact with cats and/or dogs during years 1 and 2 was different in cases (57%) and controls (65%). Therefore, flea control products were grouped as a separate category.
Individual products were also combined based on whether they were probably applied indoors or outdoors, although the questionnaire did not include specific questions about the exact location of pesticide application. As defined, indoor pesticide exposures include professional pest control service; products used to control ants, flies, cockroaches, spiders, or termites; insect repellent; and indoor foggers for fleas. Outdoor pesticide exposures include rat, mouse, gopher, or mole control products, slug or snail bait, and plant/tree insect control products.
Frequency indexes for insecticides and indoor pesticides, which were commonly administered in households, were calculated based on how often the products were used during a defined time window. For each product, scores of 0, 1, and 2 were assigned to "did not use," "used less than 5 times," and "used 5 or more times," respectively. Occasionally, when a respondent could not recall the exact frequency of use (~0.6% of all products), a score of 1.5 was assigned. The scores of individual products in each category (i.e., insecticides or indoor pesticides) were added to obtain a summary frequency index.
Statistical analysis. We performed analyses for overall leukemia and ALL separately. We used conditional logistic regression to estimate ORs and 95% confidence intervals (CI), adjusting for annual household income in U.S. dollars (three categories: < 30,000, 30,000-75,000, > 75,000).
We separated exposure history by specific periods of interest. Patients who were diagnosed during year 1 and their controls were excluded from the analysis of household pesticide exposures during year 1 and the risk of childhood leukemia, because it would be difficult to decide whether the exposures, if any, occurred before diagnosis. Similar exclusions were made for pesticide exposures during the years 2 and 3 as well, producing a smaller study population for subgroup analyses.
Cases and controls were similar regarding age, sex, race, Hispanicity, maternal education, and maternal age (Table 1). Controls have a somewhat higher annual household income.
The percentages of a variety of pesticide exposures during the index child's first year are shown in Table 2. Approximately 40% of the households used pesticides to control ants, flies, or cockroaches, whereas few families administered spider or termite control products. Individual products were grouped into several categories, including insecticides, flea control products, herbicides, indoor pesticides, and outdoor pesticides. More than half of households used insecticides or indoor pesticides during the 1-year period. The percentage of pesticide exposures during other periods varied (detailed data not shown).
Generally, the analyses of overall childhood leukemia and ALL yielded similar results. The use of professional pest control services in each of the five time frames (3 months before pregnancy, pregnancy, and years 1, 2, and 3) was more common in cases than in controls (Table 3). The ORs associated with the use of professional pest control service were > 2 for all periods except for the 3 months before pregnancy. Although the ORs for different periods were not exactly the same, a statistically significant elevated risk of leukemia was observed among children whose houses were professionally treated for pests any time during the 4-year period (OR = 2.8; 95% CI, 1.4-5.7).
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Table 3.

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The relationship between exposure to insecticides (excluding flea control products) and leukemia risk varied across the five individual time frames, with the highest OR (2.1) observed for exposure during pregnancy and the lowest OR (1.2) for exposure during year 3 (Table 3). Exposure to insecticides (excluding flea control products) any time during the 4-year period was associated with a significantly increased risk of childhood leukemia (OR = 2.1; 95% CI, 1.1-4.3). ORs for each increment in frequency index in all time frames were > 1, which is consistent with the results based on binary categorization of exposures. Compared with ORs for children who were not exposed to insecticides during the 4-year period (i.e., those who were assigned a frequency index of 0), the ORs for children who had a frequency index of 1-5 or > 5 were 1.5 (95% CI, 0.6-3.6) and 2.4 (95% CI, 1.2-5.1), respectively.
The families of controls used more flea control products than did case families, which may be due to the fact that more control families owned cats and/or dogs. The ORs associated with the use of flea control products were smaller than 1, but none were statistically significant.
Exposure to herbicides during the 4-year period was not associated with the risk of childhood leukemia, although the ORs for exposure during the 3 months before pregnancy or pregnancy were 1.8 and 1.6, respectively.
Cases were exposed to more indoor pesticides than were the controls in each of the five time frames (Figure 1). The highest OR (OR = 2.2; 95% CI, 1.3-3.6) was seen for indoor pesticide exposures during pregnancy. The association with indoor pesticide exposure during year 2 or 3 was weaker and not statistically significant. When all five time frames were combined, children who were exposed to indoor pesticides had an increased risk of leukemia (OR = 1.8; 95% CI, 1.0-3.4). Compared with ORs for children who were not exposed to indoor pesticides during the 4-year period (i.e., those who were assigned a frequency index of 0), the ORs for children who had a frequency index of 1 to 5 or > 5 were 1.4 (95% CI, 0.6-3.1) and 2.0 (1.0-4.0), respectively. Conversely, the magnitude of association between exposure to outdoor pesticides and the risk of childhood leukemia was small, and all the 95% confidence intervals of the ORs included 1 (Figure 1).
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Figure 1. Indoor and outdoor pesticide exposures and the risk of childhood ALL. The boxes are estimated ORs; vertical bars reflect upper and lower limits of 95% CIs.
*Adjusted for annual household income.
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Existing studies have generated relatively consistent results, indicating that exposure to household pesticides is associated with an increased risk of childhood leukemia, although the subtype of cases included, definition of exposure, and exposure period of interest differed ( 4-7,9-13). The results from the NCCLS provide additional strong support to the previous observations by distinguishing between the risks associated with different types of pest control, demonstrating a dose-response relationship and indicating the importance of the timing and location of exposure.
In the NCCLS, the use of professional pest control services was significantly associated with an increased risk of childhood leukemia, and the magnitude of association was larger than what was seen for general insecticide or indoor pesticide exposures. It is possible that professional pest control agencies used more concentrated and more persistent compounds, which could also be more carcinogenic. However, it is also likely that the use of professional pest control services reflects the severity of pest problems in a specific household. Professional pest control services generally apply pesticides throughout the entire house, whereas people who apply pesticides themselves are more inclined to target a specific pest infestation. In addition, it may be easier to remember accurately if the family has engaged a professional pest control service than if some family members applied pesticides themselves. Similarly, elevated ORs in the range of 1.26-2.35 were reported for professional treatment against ants and cockroaches in a recently published study of childhood ALL (12). In contrast to our findings, the use of household insecticides by professional pest control agencies was not associated with the risk of acute childhood leukemia in a German study that included more than 1,000 cases (13). However, the prevalence of the use of professional control services in the German study (2.2% in cases and 1.7% in controls) was markedly lower than what was reported in the NCCLS (33.6% in cases and 21.6% in controls from 3 months before pregnancy through the third birthday), which would result in limited statistical power to detect such an association in Germany.
Exposure to general insecticides during the first few postnatal years is associated with an increased risk of childhood leukemia in the NCCLS, which is consistent with previous studies and showed a dose-response relationship. In addition, the risk for exposure during pregnancy was higher than the risks for exposures after birth. Frequent prenatal use of household pesticides was also linked to an increased risk of ALL in another study (12). It may be inferred that the embryo or fetus is especially sensitive or susceptible to carcinogens in the environment. There is evidence that ALL is initiated in utero (14), and it has been shown that some chromosome translocation events related to the incidence of childhood ALL have a prenatal origin (15,16). An ongoing activity of the NCCLS is to determine whether selected translocations can be backtracked to birth. Correlating environmental exposures during pregnancy with chromosome translocations present at birth will likely help illustrate the natural history of childhood leukemia and the timing of key exposures and mutational events.
There is a considerable overlap between the definitions of insecticides and indoor pesticides, and the results regarding indoor pesticide use were similar to what was seen for insecticides. Reported exposure to herbicides during the 4-year period was not associated with leukemia risk, although an elevated and insignificant risk was observed for exposure before and during pregnancy. Consistent with a newly completed ecologic assessment of agricultural pesticide use and childhood leukemia conducted in California (17), no significant association between outdoor pesticide exposures and leukemia risk was observed. There could have been some misclassification in terms of indoor and outdoor pesticide use. For example, pesticides used to control rats and mice are usually applied outside of the house, but it is also possible that they are sometimes applied inside. Misclassification between indoor and outdoor exposures would have made the differences between these two categories smaller.
The NCCLS has several design features that are improvements over existing studies. Unlike several previous studies that used random digit dialing to select controls, the NCCLS employed a new protocol to select population-based controls. Controls were randomly selected from the California statewide birth registry, and a methodologic evaluation indicated that the birth certificate controls well represented the population base from which the cases arose (18). Only incident cases were included in the NCCLS, and controls were selected concurrently, which significantly reduced the lag time between diagnosis (corresponding date for controls) and interview. This should have made the reported exposure history more reliable. In contrast to many previous studies that collected data through mailed questionnaire or telephone interview, detailed history on household pesticides exposure was obtained through in-home personal interviews in the NCCLS. In addition, the NCCLS was one of the first studies specifically designed to address critical windows of exposure, that is, the timing of household pesticide exposures relative to a child's conception and development.
Recall bias cannot be ruled out in any case-control study that relies on exposures reported by the subjects, and the NCCLS is no exception. It is possible that the respondents, usually the biologic mothers, falsely claimed or forgot to mention certain exposures depending on whether the child was a patient with leukemia. However, mothers of the controls reported more usage of flea control products than the cases, which is consistent with the increased reported contact with cats and/or dogs in controls. In addition, the ORs associated with exposures to several pesticide categories varied by type and across different time frames, which provided some assurance that the observed associations were not due to general overreporting of exposures among mothers of leukemia cases, but instead may provide evidence for the effects of pesticide exposures at critical periods in a child's development.
A difference in annual household income between cases and controls was observed in this study, hence the decision to adjust for it in the analysis. In addition, a separate analysis was conducted excluding subjects with an annual income of less than $30,000, and the results were not systematically different (data not shown).
Results presented here are limited to broad types of pesticides; no specific chemicals are identified at this stage of analysis. It is certainly preferable to identify specific chemicals associated with the risk of leukemia so that preventive measures could be taken. The names of all products were recorded in the NCCLS, and the Environmental Protection Agency registration number on each of the pesticide containers will be obtained during a follow-up visit to the homes of selected cases and controls, with the ultimate goal of determining the specific chemicals rather than generic types of pesticides associated with increased risks. Based on household inventories conducted in California and Minnesota, the most common home insecticides included piperonyl butoxide, chlorpyrifos, pyrethrins, and propoxur (19,20). In California, the insecticides most frequently applied by professional pest control services for structural pest control purposes are piperonyl butoxide, pyrethrins, chlorpyrifos, and diazinon (21).
Parental occupational exposure to chemicals such as pesticides and solvents has also been suggested as a risk factor for childhood leukemia (2,13,22). Detailed occupational histories were obtained in the NCCLS, but these data are not yet available for analysis. Children living in agricultural communities can also be exposed to pesticides from agricultural use (23). Agricultural pesticide use is high in some areas of California, with over 170,000 children living in communities averaging more than 500 pounds of use per square mile for pesticides classified as probable carcinogens (24). It will be more informative when exposures from household, parental occupations and nearby agricultural applications can be evaluated jointly, which is a goal of the NCCLS. Ultimately, studies with environmental or biologic monitoring are needed to determine the relationship between pesticide exposure and childhood leukemia.
Another potential limitation of the study is the relatively small sample size, which reduces the power of the study to detect low-level risks. On the other hand, this study did consistently detect risks of 2-fold or greater, and the matched design improves the precision of statistical analyses (25). The NCCLS is currently underway and will enroll subjects until 2003. The expansion of the study population, added detail on chemical constituents, and more specific and complete exposure classification will provide more information regarding pesticide exposures and the risk of childhood leukemia.
In summary, the findings from the present study suggest that exposure to household pesticides is associated with an elevated risk of childhood leukemia and further indicate the importance of the timing and location of exposure.
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[References Listed in PubMed]
References and Notes
1. Daniels JL, Olshan AF, Savitz DA. Pesticides and childhood cancers. Environ Health Perspect 105:1068-1077 (1997).
2. Zahm SH, Ward MH. Pesticides and childhood cancer. Environ Health Perspect 106(suppl 3):893-908 (1998).
3. Davis JR. Childhood Cancer and Pesticide Use in the Home, Garden and Yard [PhD Thesis]. Berkeley, CA: Department of Entomological Sciences, University of California, Berkeley, 1991.
4. Lowengart RA, Peters JM, Cicioni C, Buckley J, Bernstein L, Preston-Martin S, Rappaport E. Childhood leukemia and parents' occupational and home exposures. J Natl Cancer Inst 79:39-45 (1987).
5. Schwartzbaum JA, George SL, Pratt CB, Davis B. An exploratory study of environmental and medical factors potentially related to childhood cancer. Med Pediatr Oncol 19:115-121 (1991).
6. Leiss JK, Savitz DA. Home pesticide use and childhood cancer: a case-control study. Am J Public Health 85:249-252 (1995).
7. Buckley J, Buckley C, Ruccione K, Sather H, Waskerwitz M, Woods W, Robison L. Epidemiological characteristics of childhood acute lymphocytic leukemia. Analysis by immunophenotype. Leukemia 8:856-864 (1994).
8. Fajardo-Gutierrez A, Garduno-Espinosa J, Yamamoto-Kimura L, Hernandez-Hernandez DM, Mejia-Arangure M, Gomez-Delgado A, Farfan-Canto JM, Ortiz-Fernandez A, Martinez-Garcia MDC. Factores de riesgo asociados al desarrollo de leucemia en niños. Bol Med Hosp Infant Mex 50:248-257 (1993).
9. Meinert R, Kaatsch P, Kaletsch U, Krummenauer F, Miesner A, Michaelis J. Childhood leukaemia and exposure to pesticides: results of a case-control study in northern Germany. Eur J Cancer 32A:1943-1948 (1996).
10. California Cancer Registry. Unpublished data.
11. Buckley JD, Robison LL, Swotinsky R, Garabrant DH, LeBeau M, Manchester P, Nesbit ME, Odom L, Peters JM, Woods WG, et al. Occupational exposures of parents of children with nonlymphocytic leukemia: a report from the Children's Cancer Study Group. Cancer Res 49:4030-4037 (1989).
12. Infante-Rivard C, Labuda D, Krajinovic M, Sinnett D. Risk of childhood leukemia associated with exposure to pesticides and with gene polymorphisms. Epidemiology 10:481-487 (1999).
13. Meinert R, Schuz J, Kaletsch U, Kaatsch P, Michaelis J. Leukemia and non-Hodgkin's lymphoma in childhood and exposure to pesticides: results of a register-based case-control study in Germany. Am J Epidemiol 151:639-646 (2000).
14. Ford AM, Ridge SA, Cabrera ME, Mahmoud H, Steel CM, Chan LC, Greaves M. In utero rearrangements in the trithorax-related oncogene in infant leukemias. Nature 363:358-360 (1993).
15. Wiemels JL, Cazzaniga G, Daniotti M, Eden OB, Addison GM, Masera G, Saha V, Biondi A, Greaves MF. Prenatal origin of acute lymphoblastic leukaemia in children. Lancet 354:1499-1503 (1999).
16. Wiemels JL, Ford AM, Wering ERV, Postma A, Greaves M. Protracted and variable latency of acute lymphoblastic leukemia after TEL-AML1 gene fusion in utero. Blood 94:1057-1062 (1999).
17. Reynolds P, Von Behren J, Gunier R, Goldberg D, Hertz A, Harnly M. Childhood cancer and agricultural pesticide use: an ecological study in California. Environ Health Perspect 110:319-324 (2002).
18. Ma X, Layefsky M, Reynolds P, Buffler PA. Strategies for control selection in case-control studies: an evaluation of two methods [Abstract]. Am J Epidemiol 153:S258 (2001).
19. Robinson J, Pease W, Albright D, Morello-Frosch R. Pesticides in the Home and Community: Health Risks and Policy Alternatives. Berkeley, CA: California Policy Seminar, 1994;85-91.
20. Adgate JL, Kukowski A, Stroebel C, Shubat PJ, Morrell S, Quackenboss JJ, Whitmore RW, Sexton K. Pesticide storage and use patterns in Minnesota households with children. J Expos Anal Environ Epidemiol 10:159-167 (2000).
21. California Department of Pesticide Regulation. Environmental Monitoring and Pest Management Branch. Pesticide Use Reporting Data 1998. Data file. Sacramento, CA:California Department of Pesticide Regulation, 1999.
22. Shu XO, Stewart P, Wen W-Q, Han D, Poter JD, Buckley JD, Heineman E, Robison LL. Parental occupational exposure to hydrocarbons and risk of acute lymphocytic leukemia in offspring. Cancer Epidemiol Biomarkers Prev 8:783-791 (1999).
23. Lu C, Fenske RA, Simcox NJ, Kalman D. Pesticide exposure of children in an agricultural community: evidence of household proximity to farmland and take home exposure pathways. Environ Res 84:290-302 (2000).
24. Gunier RB, Harnly ME, Reynolds P, Hertz A, Von Behren J. Agricultral pesticide use in California: pesticide prioritization, use densities, and population distributions for a childhood cancer study. Environ Health Perspect 109:1071-1078 (2001).
25. Cochran W. Planning and Analysis of Observational Studies. New York:John Wiley and Sons, 1983.
Last Updated: August 13, 2002
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