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. Author manuscript; available in PMC: 2014 Nov 1.
Published in final edited form as: Environ Int. 2013 Oct 3;61:57–63. doi: 10.1016/j.envint.2013.09.007

Pyrethroids in house dust from the homes of farm worker families in the MICASA study

Kelly J Trunnelle a,*, Deborah H Bennett b, Daniel J Tancredi c, Shirley J Gee d, Maria T Stoecklin-Marois b, Tamara E Hennessy-Burt b, Bruce D Hammock d, Marc B Schenker b
PMCID: PMC4059492  NIHMSID: NIHMS582235  PMID: 24096042

Abstract

Indoor pesticide exposure is a growing concern, particularly for pyrethroids, a commonly used class of pesticides. Pyrethroid concentrations may be especially high in homes of immigrant farm worker families, who often live in close proximity to agricultural fields and are faced with poor housing conditions, potentially causing high pest infestation and pesticide use. We investigate levels of pyrethroids in the house dust of farm worker family homes in a study of mothers and children living in Mendota, CA, within the population-based Mexican Immigration to California: Agricultural Safety and Acculturation (MICASA) Study. We present pesticide use data and levels of pyrethroid pesticides in indoor dust collected in 2009 as measured by questionnaires and a GC/MS analysis of the pyrethroids cis- and trans-permethrin, cypermethrin, deltamethrin, esfenvalerate and resmethrin in single dust samples collected from 55 households. Cis- and trans-permethrin had the highest detection frequencies at 67%, with median concentrations of 244 and 172 ng/g dust, respectively. Cypermethrin was detected in 52% of the homes and had a median concentration of 186 ng/g dust. Esfenvalerate, resmethrin and deltamethrin were detected in less than half the samples. We compared the pyrethroid concentrations found in our study to other studies looking at both rural and urban homes and daycares. Lower detection frequencies and/or lower median concentrations of cis- and trans-permethrin and cypermethrin were observed in our study as compared to those studies. However, deltamethrin, esfenvalerate and resmethrin were detected more frequently in the house dust from our study than in the other studies. Because households whose children had higher urinary pyrethroid metabolite levels were more likely to be analyzed in this study, a positive bias in our estimates of household pyrethroid levels may be expected. A positive association was observed with reported outdoor pesticide use and cypermethrin levels found in the indoor dust samples (rs = 0.28, p = 0.0450). There was also a positive association seen with summed pyrethroid levels in house dust and the results of a pesticide inventory conducted by field staff (rs = 0.32, p = 0.018), a potentially useful predictor of pesticide exposure in farm worker family homes. Further research is warranted to fully investigate the utility of such a measure.

Keywords: Pyrethroids, House dust, Farm worker, Pesticide inventory

1. Introduction

A number of pyrethroids, such as permethrin, cypermethrin, deltamethrin, and esfenvalerate, have been reported to be present in house dust with detection frequency (%D) ranges from various studies of 45–100%, 5–64%, 5–17% and 5–29%, respectively (Bradman et al., 2007; Colt et al., 2004; Hwang et al., 2008; Julien et al., 2008; Morgan et al., 2007; Quirós-Alcalá et al., 2011; Rudel et al., 2003; Starr et al., 2008). Much of this data was collected before or in the same year as the federally mandated phase-out of residential uses of the organophosphate pesticides chlorpyrifos and diazinon in 2001, which subsequently caused household pyrethroid use to increase (Horton et al., 2011; USEPA, 2001, 2012; Williams et al., 2008). This can be seen in the above mentioned studies, with the highest %Ds of pyrethroids occurring in studies whose samples were collected during or after 2001. Although pyrethroids have low toxicity, particularly compared to other insecticides, studies have shown that high levels of exposure to pyrethroids may cause significant toxicity and health effects, including acute neurotoxic effects (Costa et al., 2008; Ray and Fry, 2006), immunotoxic effects (Blaylock et al., 1995; Emara and Draz, 2007) and negative effects on mammalian reproduction (Ji et al., 2011; Zhang et al., 2008). Pyrethroids are also possible human carcinogens (USEPA, 2006).

Families living in close proximity to farms may have higher than average pyrethroid exposure due to household pesticide use, drift from agricultural application and take-home exposure pathways from occupational use by another family member (Curl et al., 2002; Harnly et al., 2005; Lu et al., 2000; You et al., 2004). High levels of pesticides in carpet dust are a particular concern for young children who, due to their continual exploration of their environments, spend a large amount of time on the floor and have increased hand to mouth activity, resulting in increased exposure to pollutants through dermal and non-dietary ingestion routes (Fenske et al., 1990; Gurunathan et al., 1998; Moya et al., 2004; Zartarian et al., 1997). These two factors combined make children living in agricultural communities especially susceptible to pesticide exposure (Arcury et al., 2007; Bradman et al., 2007). Data on pyrethroid concentrations in the house dust of rural farm worker homes is limited.

This study was conducted in order to address participant concerns about pesticide exposure in the community-based Mexican Immigration to California: Agricultural Safety and Acculturation (MICASA) study. Our objectives were to characterize the levels of pyrethroid pesticides in the house dust of farm worker families and characterize their residential pesticide application practices in order to evaluate possible associations between the dust levels and pesticide use practices. We report the pesticide use data and levels of pyrethroid pesticides in indoor dust collected in 2009 as measured by questionnaires and dust concentrations of the pyrethroids cis- and trans-permethrin, cypermethrin, deltamethrin, esfenvalerate and resmethrin among 55 households of farm worker families living in Mendota, CA.

2. Material and methods

2.1. Sample size

Single dust samples were collected from 105 homes of families participating in the MICASA study. Of the 105 available samples, 70 had sufficient quantities of dust after sieving for instrumental analysis of pyrethroids. Of those, there were 55 samples selected, with relatively higher selection probabilities assigned to those households with elevated levels of the common pyrethroid urinary metabolite 3-phenoxybenzoic acid (3PBA) in urine samples collected from the children in order to increase the probability of having detectable levels of pyrethroids in the dust. Data on the 55 dust samples that were analyzed are presented here. Data on urine concentrations will be reported in a future publication.

2.2. Study population

The MICASA study is a prospective cohort sample of 467 hired farm worker family households from Mendota, CA, designed to evaluate occupational and environmental exposures of significance for a farm worker population. Households were sampled from randomly selected census blocks and, following door-to-door enumeration, those households containing at least one hired farm worker were contacted for recruitment. Eligible participants in the MICASA study were men and women, residing in Mendota, CA, ages 18–55 years, self-identified as Mexican or Central American, and with at least one household member who worked in agriculture 45 days or more in the previous year, with both members of the household completing the interview (Stoecklin-Marois et al., 2011).

MICASA recruitment was conducted between January 2006 and May 2007. Recruitment for the home pyrethroid exposure study began in February of 2009, and sample collection took place between June and December of 2009.

The analysis highlighted in this paper was designed to look at levels of pyrethroid pesticides in the homes of the MICASA study population. Because children typically have higher levels of exposure to pesticides (Moya et al., 2004), we restricted eligibility to those MICASA families with at least one child aged 7 or under at the time of recruitment in order to better understand pyrethroid sources in this potentially highly exposed population. Among the MICASA households completing baseline interviews, 175 (37.5%) were eligible for participation in the homepyrethroid exposure study. Eligible households were listed in random order for contact. One hundred twenty seven households were contacted for recruitment before reaching our goal of 105 (82.7%) households who agreed to participate and were enrolled in the study. The remaining 22 households either could not be contacted or declined to participate. If a family had multiple eligible children, one child was randomly selected and enrolled. At the time of sample collection, children ranged from 2 to 8 years of age.

Written informed consent was obtained from each participant. Each study component was described verbally and in writing to the participant prior to obtaining written informed consent. Spanish was the primary language of the participants, thus the study description and written informed consent were provided in Spanish. All study procedures were approved by the University of California, Davis, Institutional Review Board.

2.3. Sample collection

Dust samples were collected and questionnaires were conducted between June and December of 2009. Dust samples were collected in the main living area of the home, which was defined as the most frequently used room in the house that was not a bedroom or kitchen. Dust samples were collected using a Eureka Mighty-Mite vacuum cleaner and standard crevice tool attachment (Model 3670) modified to collect dust into a 19 × 90 mm cellulose extraction thimble (Whatman Inc.) that was secured to the crevice tool using a rubber O-ring. More detailed information on collection methods using the Eureka Mighty-Mite have been described elsewhere (Allen et al., 2008; Rudel et al., 2003). The square footage of the main living area was measured and recorded as well as the temperature and humidity. Dust was collected over the equivalent of the entire measured floor area. Once sampling was complete, the thimble was removed from the Mighty Mite, wrapped in cleaned foil, weighed, placed in a polyethylene zip-top bag and labeled with the household ID number. Dust samples were then refrigerated at the MICASA field office for generally less than one day and delivered on ice to UC Davis, where they were stored in a −20 °C freezer until sample extraction and analysis. All Mighty-Mite equipment was cleaned using a 1% solution of detergent and hot water and allowed to air-dry between home visits in order to prevent cross-contamination.

At the time of sample collection, a questionnaire was administered to the mothers. We obtained the frequency of pesticide use in both the hot and cold season of the previous year, including sprays, foggers, sticky traps, bait traps, gels, and any application by professional exterminators. Participants were asked if anyone living in the home had seen rodents, rodent feces, live or dead roaches, roach feces or ants inside the home at any time in the last year, with answer options including: large amounts, moderate amounts, none or don't know. On the day of dust collection a staff member conducted a pesticide inventory in which detailed information on all pesticide products in the home was recorded, this included the name of each product, the size of the product container, the EPA registration number and all active ingredients.

2.4. Preparation of dust extracts

All dust and materials contained in each cellulose thimble were removed and weighed. The particulates were then sieved, first to 1500 µm, and then to 150 µm for analysis. The dust samples were extracted using a method similar to that described in Starr et al. (2008). Briefly, dust samples were each weighed to 0.5 g aliquots, spiked with 250 ng of 13C6-labeled trans-permethrin, the surrogate recovery standard (SRS), and vortexed with 12 mL hexane. Samples were sonicated for 20 min, centrifuged at 3000 rpm for 10 min, decanted and volume reduced to 2 mL hexane. The extracts were subjected to alumina:silica gel (1:1 by weight) column chromatography to remove interferences following methods similar to those described in Hwang et al. (2008). Prior to use, alumina and sodium sulfate were heated (450 °C for 4 h) as well as the silica gel (170 °C for 24 h). All heated products were stored at 130 °C. When needed, alumina was deactivated (4% by weight) with purified water. The columns were conditioned with hexane and eluted with 50 mL of dichloromethane:hexane (1:1) mixture. The eluted solvents were concentrated to 1 mL of hexane, and the internal standard (IS) phenanthrene-d10 was added.

2.5. Instrumental analysis

Dust extracts were analyzed by gas chromatography mass spectrometry (GC/MS) operated in selected ion mode (Hewlett-Packard 6890 GC with a Hewlett-Packard 5873 mass spectral detector). Multiple ions, including one used for quantitation and one to two for qualification and confirmation, were monitored for each compound. Calibration curves for all analytes were generated using the response ratio of each quantitation ion to the quantitation ion of the IS. Individual pyrethroid pesticide stock solutions (100 µg/mL in methanol) for permethrin, cypermethrin, deltamethrin, esfenvalerate, and resmethrin were obtained from AccuStandard (New Haven, CT). Concentrations of the pyrethroid standards ranged from 62.5 to 2000 ng/mL. All samples and standards contained 100 ng of the IS. For each analyte and standard, confirmation of the identity was based upon the retention time and the presence and correct ratio of qualifier ions relative to the ion used for quantitation. The chromatographic column used was a J&W DB-5MS fused silica capillary column (30 m × 0.25 mm ID, 0.25 µm film thickness) with a helium flow rate of 1 mL/min. The injection temperature was 280 °C, with the initial GC oven temperature set to 80 °C and ramped to 100 °C at 20 °C/min, then 300 °C at 10 °C/min, and maintained for 10 min. The total run time for the analysis of each sample was 31 min. In this analysis, cis- and trans-isomers are only reported for permethrin and its metabolites. All other pesticides and metabolites are reported as summed totals of all isomers.

2.6. Statistical analysis

Summary statistics for the pyrethroid data were calculated. For concentrations below the limit of detection (LOD), an imputed value was assigned equal to the LOD divided by the square root of 2 (Barr et al., 2010; Hornung and Reed, 1990). A Spearman rank-order correlation procedure was used to determine the intra-household correlations between particular pyrethroid concentrations, with significance set at p < 0.05.

A Spearman rank-order correlation procedure and 95% confidence intervals (CI) were used to evaluate associations between interview questionnaire variables and the presence of pyrethroid pesticides in the house dust, with significance set at p < 0.05.

As part of the main MICASA study questions on pesticide use were asked of the full cohort of 436 households in both an interview conducted from January 2006 to May 2007 and an interview conducted from February 2009 to June 2010. These questions were asked of both the male and female heads of household. Responses to these questions allowed us to look at the consistency of reporting pesticide use among family members as well as the consistency of reporting pesticide use over time. In both interviews the male and female heads of household were asked separately if either they or anyone in the household uses indoor and/or outdoor pesticide sprays. The consistency of responses to these pesticide use questions between the men and women from the same household was assessed using Cohen's kappa, a measure of chance-corrected agreement (Landis and Koch, 1977; Lin et al., 2011). Temporal comparisons from the same participant between the two interviews conducted approximately 3 years apart were also made using Cohen's kappa.

All statistical analyses were performed using SAS version 9.2 (SAS Institute, Cary, NC).

3. Results

3.1. Population demographics & questionnaire

The demographics of the entire MICASA population, as well as the 55 participating households whose dust was analyzed can be seen in Table 1. The participants in the MICASA study ranged in age from 18 to 83 years old, while those participants whose house dust is reported on here ranged in age from21 to 55 years old at the time of the baseline interview. A chi-square test of independence was performed to examine the relation between age and participation in this portion of the study. Participants whose house dust is reported on here were significantly younger than the rest of the MICASA population (χ2 (3, N = 875) = 82.7, p < 0.0001). MICASA participants had very low educational levels, with 68.7% of the male participants and 58.7% of the female participants having only a 6th grade education or lower, while those participating in this portion of the study had significantly higher educational levels than the rest of the MICASA population (χ2 (2, N = 875) = 7.2, p = 0.03). The MICASA population was almost all married, with 100% of those that participated in the portion of the being married, significantly more than those in the main MICASA population (χ2 (2, N = 875) = 13.6, p = 0.001). Most of the MICASA participants were born in either Mexico or El Salvador, with only 3.9 and 5.2% of the male and female participants, respectively, being born in the United States, there was no significant difference in the birth country of those participating in this study.

Table 1.

Socio-demographic characteristics of all participants in the MICASA study and those who also participated in the Home Pesticide Study assessed on the MICASA baseline interview, 2006–2007.

All baseline participants Home pesticide
participants


N (%) Male Female Male Female
Age range
  18–30 111 (25.5) 130 (29.6) 23 (44.2) 27 (49.1)
  31–40 145 (33.3) 168 (38.2) 21 (40.4) 25 (45.5)
  41–45 64 (14.7) 63 (14.3) 6 (11.5) 3 (5.4)
  46+ 115 (26.5) 79 (17.9) 2 (3.9) 0 (0.0)
Education
  No school 18 (4.6) 16 (4.1) 0 (0.0) 3 (6.4)
  ≤6th grade education 252 (64.1) 212 (54.6) 31 (67.4) 17 (36.2)
  >6th grade education 123 (31.3) 160 (41.3) 15 (32.6) 27 (57.4)
Marital status
  Married 413 (95.2) 411 (93.4) 55 (100) 55 (100)
  Divorced/separated/widow 4 (0.9) 15 (3.4) 0 (0.0) 0 (0.0)
  Single 17 (3.9) 14 (3.2) 0 (0.0) 0 (0.0)
Country of birth
  United States 17 (3.9) 23 (5.2) 1 (1.9) 1 (1.8)
  Mexico 279 (64.1) 296 (67.3) 34 (65.4) 37 (67.3)
  El Salvador 126 (29.0) 107 (24.3) 16 (30.8) 17 (30.9)
  Honduras/Nicaragua/Guatemala 13 (3.0) 14 (3.2) 1 (1.9) 0 (0.0)

3.2. Pyrethroid concentrations in house dust

Of the five pyrethroids tested for, at least one pyrethroid, generally permethrin, was detected in 89% of the dust samples. Detection frequencies (%Ds) for the individual pyrethroids were variable among the dust samples, and ranged from 20 to 67% (Table 2). Cis- and trans-permethrin had the highest %D at 67% with median concentrations of 244 and 172 ng/g dust, respectively, and an average ± standard deviation (SD) cis- to trans-permethrin ratio of 1.8 ± 1.1. Cypermethrin had the next highest %D at 52% and median concentration of 186 ng/g dust. Deltamethrin, esfenvalerate, and resmethrin were detected in less than half the samples.

Table 2.

Detection frequencies, select percentiles and maximum pyrethroid concentrations reported permass dust (ng/g) and per surface area (ng/m2) from the MICASA Home Pesticide Study, 2009 (n = 55).

Pyrethroid %D 50th 75th 90th 95th Max
ng/g dust Cis-permethrin 67 244 568 670 755 1410
Trans-permethrin 67 172 207 274 421 1737
Cypermethrin 52 186 590 3223 7036 15,059
Esfenvalerate 44 <LOD 246 426 454 585
Resmethrin 29 <LOD 161 208 261 964
Deltamethrin 20 <LOD <LOD 250 385 701
ng/m2 Cis-permethrin 67 16 22 36 56 80
Trans-permethrin 67 5.7 6.7 9.3 14 98
Cypermethrin 52 18 63 175 334 516
Esfenvalerate 44 <LOD 12 15 16 19
Resmethrin 29 <LOD 5.2 6.1 6.6 54
Deltamethrin 20 <LOD <LOD 13 15 16

Multiple intra-household correlations between particular pyrethroid concentrations were found to be statistically significant (Table 3). The correlation of the cis- and trans-permethrin isomers was significant with a Spearman rank correlation coefficient (rs) of 0.81, p < .0001. All other correlations between pyrethroids that were statistically significant (p < 0.05) had rs values below 0.5.

Table 3.

Relationship between individual pyrethroid concentrations found in house dust (N = 55 households) using the Spearman rank correlation coefficient (p-value).

cis-
Permethrin
trans-
Permethrin
Total
permethrin
Cypermethrin
trans-Permethrin 0.81 (<.0001)
Total permethrin 0.98 (<.0001) 0.88 (<.0001)
Cypermethrin 0.26 (0.054) 0.32 (0.019) 0.27 (0.049)
Esfenvalerate 0.43 (0.0012) 0.37 (0.0055) 0.45 (0.00050) 0.30 (0.025)

3.3. Correlation of interview data with measured concentrations in dust

In the field staff-collected pesticide inventory, 29.1% of the homes had at least one bottle of residential pesticide present. In the participant interview, 30.2% of the women reported using outdoor spray pesticides and 34.6% reported using indoor pesticide sprays. Many women reported pest problems, with 25.5% reporting rodents, 36.4% reporting roaches and 40.0% reporting ants.

Univariate analysis showed multiple questionnaire variables to significantly correlate with pyrethroid concentrations (Table 4). The number of pesticide products in each home, as determined by the pesticide inventory was found to be a significantly positive correlate of the sum of pyrethroid concentrations found in the house dust. The reported use of outdoor pesticide sprays, based on average annual frequency significantly correlated with increased levels of both the sum of pyrethroids and cypermethrin. When the use of outdoor pesticide sprays was split into three categories: no annual use, 1–2 times/year and more than 3 times/year, significant positive correlations were still seen with levels of summed pyrethroids and cypermethrin. The reported amount of roaches present in the home was negatively correlated with the summed pyrethroid concentrations, as well as the esfenvalerate concentrations in the house dust. Permethrin concentrations in the house dust were positively correlated with the reported amount of rodents in the home.

Table 4.

Spearman rank correlation analysis results showing the relationship between pyrethroid concentrations and various pesticide use and questionnaire items.

Sum pyrethroids Permethrin Cypermethrin Esfenvalerate




Variable rs (95% CI) p > lrl rs (95% CI) p > lrl rs (95% CI) p > lrl rs (95% CI) p > lrl

Pesticide Inventory 0.32 (0.05–0.53) 0.018 0.21 (−0.06–0.45) 0.12 0.20 (−0.07–0.44) 0.13 0.21 (−0.07–0.44) 0.13
Outdoor spraysa 0.23 (−0.04–0.47) 0.096 0.18 (−0.10–0.42) 0.21 0.28 (0.00–0.51) 0.0450 0.06 (−0.21–0.32) 0.67
Roachesb −0.23 (−0.47–0.04) 0.090 −0.12 (−0.37–0.15) 0.40 −0.11 (−0.36–0.16) 0.43 −0.23 (−0.46–0.04) 0.092
Rodentsb 0.08 (−0.19–0.34) 0.57 0.23 (−0.04–0.47) 0.096 −0.04 (−0.30–0.24) 0.80 0.04 (−0.23–0.31) 0.76
Antsb 0.14 (−0.13–0.39) 0.30 0.20 (−0.07–0.44) 0.10 0.02 (−0.25–0.29) 0.90 0.04 (−0.23–0.31) 0.80

Bold text: p < 0.1, Gray box: p < 0.05.

a

Based on frequency of use during previous year.

b

Based on categorical amount: large amount, moderate amount, none.

3.4. Consistency of responses to pesticide use questionnaires

The levels of agreement of responses to pesticide use questions, asked of the main MICASA cohort during two separate interviews conducted in 2006–2007 and 2009–2010, between men and women from the same household were found to be moderately high, with Cohen kappa values ranging from 0.56 to 0.76 (Table 6). In the 63 of 436 households (17%) in which either the man or the woman reported using outdoor pesticide sprays during the first interview, use was reported by both the man and the woman in 28 households (44%), with approximately equal proportions of only the man or only the woman reporting pesticide use (Cohen's kappa = 0.56, 95% CI: 0.43–0.69). There was higher estimated consistency for indoor sprays in the first interview (Cohen's kappa = 0.76, 95% CI: 0.67–0.85).

Table 6.

Comparison of pesticide use reporting between adult male and female members of the same household for both the baseline and follow-up interviews.

Total
N
Both no
Cell N (%)
Users
N
Both yes
Cell N (% of users)
Women yes,
Men no
Cell N (% of users)
Men yes,
Women no
Cell N (% of users)
Cohen's kappa
(95% CI)
Baseline Outdoor spray 373 310 (83) 63 28 (44) 18 (29) 17 (27) 0.56 (0.43–0.69)
Indoor sprays 364 292 (80) 72 48 (67) 9 (12) 15 (21) 0.76 (0.67–0.85)
Follow-up Outdoor spray 282 163 (58) 119 67 (56) 25 (21) 27 (23) 0.58 (0.48–0.68)
Indoor sprays 282 186 (66) 96 51 (53) 23 (24) 22 (23) 0.59 (0.48–0.69)

There was only slight consistency in how a given participant answered both the indoor and outdoor pesticide use questions when asked the same questions at the two interviews conducted approximately 3 years apart (Table 7), with Cohen's kappa estimates ranging from 0.08 to 0.15. A larger fraction of the population reported using pesticides at the second interview than at the first interview, with between 20.0 and 26.9% of individuals reporting use at the second that did not report at the first, in contrast to the 5.4 to 11.3% of individuals reporting use at first but not at the second. Only between 5.6 and 6.7% of individuals reported use for both time periods. When answers from both men and women were combined to show if either one had reported pesticide use, results were slightly higher with 7.3 and 7.7% reporting use of indoor and outdoor sprays at both interviews.

Table 7.

Temporal comparison of pesticide use reporting per individual participant between the baseline vs. follow-up interviews.

Baseline

Yes No Yes No Yes No



Cell N (% of total) Men indoor,
N = 275
Women indoor,
N = 337
Man and/or woman indoor,
N = 467
Indoor
Follow-up Yes 16 (6) 55 (20) 22 (6) 71 (21) 34 (7) 86 (18)
No 31 (11) 173 (63) 36 (11) 208 (62) 56 (12) 291 (62)
Cohen's kappa (95% CI) 0.08 (−0.04–0.20) 0.10 (−0.01–0.21) 0.13 (0.04–0.23)
Cell N (% of Total) Men outdoor,
N = 276
Women outdoor,
N = 342
Man and/or woman outdoor,
N = 467
Outdoor

Yes 17 (6) 72(26) 23 (7) 92 (27) 36 (8) 108 (23)
No 15 (6) 172 (62) 19 (5) 208 (61) 40 (8) 283 (61)
Cohen's kappa (95% CI) 0.13 (0.03–0.24) 0.14 (0.04–0.23) 0.15 (0.06–0.24)

4. Discussion

We assessed the levels of pyrethroid pesticides in 55 homes in a farm worker population by laboratory measurements of permethrin, cypermethrin, resmethrin, esfenvalerate and deltamethrin in house dust samples and by questionnaire data. This population had a relatively low educational level, with less than half of the participants reporting a 6th grade education or higher, in contrast to the 85% of U.S. adults who have a high school diploma (Stoops, 2004).

Detectable levels of the common pyrethroids permethrin, cypermethrin, deltamethrin, esfenvalerate and resmethrin were found in the dust samples collected in this study. Most of these pyrethroids have been detected in house dust from several different studies (Table 5). The majority of these studies were conducted with the general population and two were conducted with farm working communities; however there was little difference between pyrethroid concentrations in the house dust from the two types of populations. We observed lower detection frequencies and/or lower median concentrations of cis- and trans-permethrin than many of these studies (Bradman et al., 2007; Colt et al., 2004; Hwang et al., 2008; Julien et al., 2008; Morgan et al., 2007; Quirós-Alcalá et al., 2011; Starr et al., 2008). We also observed lower or comparable detection frequencies and median concentrations of cypermethrin in our study as compared to others (Bradman et al., 2007; Hwang et al., 2008; Julien et al., 2008; Quirós-Alcalá et al., 2011; Rudel et al., 2003; Starr et al., 2008). Deltamethrin and esfenvalerate were detected more frequently in the house dust from our study than in any other (Bradman et al., 2007; Julien et al., 2008; Quirós-Alcalá et al., 2011; Starr et al., 2008). Only two other studies looked at resmethrin in house dust, and neither was able to find detectable levels (Bradman et al., 2007; Julien et al., 2008) compared to the 29% detection in our study. The differences in detection frequencies in our study as compared to these other studies may be the result of different LODs. Additionally, our study population was restricted to only those families with young children, potentially causing differences in pesticide use practices when compared to a more diverse population containing people of differing ages, marital statuses, and living arrangements. Also, because we weighted our sample selection to those households whose participants already showed exposure to pyrethroids, a true random sampling from our study population may have exhibited lower detection frequencies than what has been reported here. We also did not observe the seemingly extreme outliers or maximum concentrations several orders of magnitude over the median concentration that some of the other studies reported (Julien et al., 2008; Morgan et al., 2007; Quirós-Alcalá et al., 2011; Rudel et al., 2003; Starr et al., 2008). This may be due to our study population being better trained in pesticide use practices and precautions from work in agriculture than urban dwellers.

Table 5.

Summary statistics for pyrethroid concentrations (ng/g) in dust from multiple studies.

Pyrethroid (ng/g) cis-Permethrin trans-Permethrin Cypermethrin Deltamethrin Esfenvalerate Resmethrin







Study Year N %D 50th 95th Max % 50th 95th Max %D 50th 95th Max %D 50th 95th Max %D 50th 95th Max %D 50th 95th Max
MICASA, Farmworker Families, Mendota, CA 2009 55 67 244 755 1410 67 172 421 1737 52 186 7036 15059 20 <LOD 385 701 44 <LOD 454 585 29 <LOD 261 964
Urban & Rural CA, Quirós-Alcalá et al. (2011) 2006
  Oakland 13 100 291 21600 26700 100 504 36400 46800 64 587 5990 13100 12 <LOD 13000 16300 ND
  Salinas 15 100 568 5930 6300 100 952 9170 9690 55 230 4540 13500 17 <LOD 3780 5590 3 <LOD <LOD 67
Davis, CA Apartments, Hwang et al. (2008) 2004 11 91 52 319a NR 91 126 680a NR 91 177 1033a NR
Farmworker Families, Salinas, Bradman et al. (2007) 2002 20 100 210 NR 2900 100 570 NR 5800 40 100 NR 1500 5 <LOD NR 560 5 <LOD NR 50 ND
Urban Public Housing, Boston, Julien et al. (2008) 2002–2003 35 100b 920b NR 13100b 60 300 NR 5200 9 <LOD NR 7000 29 <LOD NR 1200 ND
Ohio Preschool Children - homes, Morgan et al. (2007) 2001 120 100 470 7630 79600 100 344 9210 78800
Ohio & N. Carolina Homes & Daycares, Starr et al. (2008) 2000–2001 85 100 666 14122 30553 100 711 11980 30420 34 <LOD 1571 6492 5 <LOD <LOD 2503 8 <LOD 60 943
National Cancer Institute, Colt et al. (2004) 1999–2001 513 72 337c NR NR 74 517c NR NR
Cape Cod, MA Homes, Rudel et al. (2003) 1999–2001 119 45 <LOD NR 61900 53 387 NR 98000 5 <LOD NR 172000
a

90th percentiles reported.

b

Total permethrin reported.

c

Geometric mean reported.

We wanted to examine the potential reasons for the lack of correlations with the questionnaire data. We used data from the main MICASA study questions on pesticide use, which were asked of the full cohort of 436 households in two interviews, the first conducted from January 2006 to May 2007 and the second from February 2009 to June 2010. The consistency of responses to these pesticide use questions between the men and women from the same household was assessed and within-household levels of agreement were moderately high. Use was reported by both the man and the woman in 44% of the households in which either the man or the woman reported using outdoor pesticide sprays during the first interview. Assuming pesticides were actually applied if reported by either the man or the woman, asking only the man or the woman would misclassify many of the households that used pesticides as non-users, which may be partially responsible for the lack of correlation. Temporal comparisons from the same participant between the two interviews conducted approximately 3 years apart were also made. A larger fraction of the population reported using pesticides at the second interview than at the first interview, with only between 5.6 and 6.7% of individuals reporting use for both time periods. The low levels of agreement could be due either to actual changes in use patterns or due to differences in reporting and may also be partially responsible for the lack of correlation between questionnaire responses and house dust concentrations.

Many previous studies have reported that residential pesticide use questions were ineffective at identifying exposure levels (Sexton et al., 2003). We also saw a lack of consistency in the relationships between questionnaire data and measured levels of pyrethroids in the house dust (Table 4). There was a positive correlation with reported outdoor pesticide use and pyrethroid levels in the house dust. However there was no relationship with indoor pesticide use. We found a slightly negative correlation with outdoor traps and levels of indoor pyrethroids, suggesting that families that use traps to reduce their pest problems use less pesticide in their homes. A possible reason for the lack of correlations between reported pesticide use (especially indoor pesticide use) and pyrethroid levels found in the home is that the questionnaire asked about any pesticide products used for insect control, while we only measured five specific pyrethroid compounds. It is very likely that products used contained other pyrethroids' active ingredients as well. There are also likely to be large discrepancies in the amount of pesticide applied, as well as cleaning practices between participants. This information was not accounted for in our questionnaire.

The most promising predictor of exposure was the pesticide inventory. There was a significant correlation between the pesticide inventory and the sum of pyrethroid concentrations found in the house dust. With traditional questionnaires, it is often difficult for participants to accurately recall pesticide use. The pesticide inventory on the other hand is relatively easy data to collect, requiring only a few minutes time for the interviewer to note the pesticide products present in the participant's homes. Although neither method gives information on what, or the concentrations of, specific pesticides that may be found in the physical samples from the home, the pesticide inventory may be a more useful tool to predict possible pesticide exposure than the traditional participant recall.

This study has many limitations. Data from households with higher levels of dust or whose children had higher pyrethroid metabolite levels in the urine were more likely to be analyzed, which can be expected to lead to a positive bias in our estimates of household pyrethroid levels. Our small sample size limited the statistical power and may have prevented us from observing statistically significant correlations in our data. Additionally, as mentioned above, there was a lack of consistent reporting of pesticide applications between husband and wife.

Despite these limitations, this study contributes to existing research by providing further evidence that farm working families face exposures to pyrethroid pesticides. These results can be used to develop interventions to reduce pesticide exposure in vulnerable populations. Additionally, this study provides evidence that a pesticide inventory may be a more useful tool in estimating possible pesticide exposure than traditional pesticide use questionnaires have been in the past. Further research is warranted to fully investigate the usefulness of such a measure.

Acknowledgments

We acknowledge Hyun-Min Hwang for his assistance with the laboratory analysis; Lisa Tang for her assistance in both the field and the lab; the local field staff, particularly Gloria Andrade, Ana Cervantes, Alex Cervantes and Giselle Garcia, for all of their efforts; and all of the participants. Funding from The California Endowment and the National Institute of Occupational Safety and Health, 2U50OH007550 and 1R01OH009293, and the NIEHS Superfund Research Program, P42ES04699 supported this research. Bruce D. Hammock is a George and Judy Marcus Senior Fellow of the American Asthma Society.

Abbreviations

MICASA

, Mexican Immigration to California: Agricultural Safety and Acculturation

3PBA

3-phenoxybenzoic acid

SRS

surrogate recovery standard

IS

internal standard

GC/MS

gas chromatographymass spectrometry

LOD

limit of detection

CI

confidence intervals

%D

detection frequencies

SD

standard deviation

rs

Spearman rank correlation coefficient

Contributor Information

Kelly J. Trunnelle, Email: kjtrunnelle@ucdavis.edu.

Deborah H. Bennett, Email: dhbennett@phs.ucdavis.edu.

Daniel J. Tancredi, Email: daniel.tancredi@ucdmc.ucdavis.edu.

Shirley J. Gee, Email: sjgee@ucdavis.edu.

Maria T. Stoecklin-Marois, Email: mtstoecklin@phs.ucdavis.edu.

Tamara E. Hennessy-Burt, Email: tehennessy@phs.ucdavis.edu.

Bruce D. Hammock, Email: bdhammock@ucdavis.edu.

Marc B. Schenker, Email: mbschenker@phs.ucdavis.edu.

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