Children's Health Volume 122  Issue 7  July 2014
Environ Health Perspect; DOI:10.1289/ehp.1307072
The Influence of Declining Air Lead Levels on Blood Lead–Air Lead Slope Factors in Children
Jennifer RichmondBryant,^{1} Qingyu Meng,^{2} Allen Davis,^{1} Jonathan Cohen,^{3} ShouEn Lu,^{2} David Svendsgaard,^{1} James S. Brown,^{1} Lauren Tuttle,^{4} Heidi Hubbard,^{3} Joann Rice,^{5} Ellen Kirrane,^{1} Lisa C. VinikoorImler,^{1} Dennis Kotchmar,^{1} Erin P. Hines,^{1} and Mary Ross^{1}

Background: It is difficult to discern the proportion of blood lead (PbB) attributable to ambient air lead (PbA), given the multitude of lead (Pb) sources and pathways of exposure. The PbB–PbA relationship has previously been evaluated across populations. This relationship was a central consideration in the 2008 review of the Pb national ambient air quality standards.
Objectives: The objectives of this study were to evaluate the relationship between PbB and PbA concentrations among children nationwide for recent years and to compare the relationship with those obtained from other studies in the literature.
Methods: We merged participantlevel data for PbB from the National Health and Nutrition Examination Survey (NHANES) III (1988–1994) and NHANES 9908 (1999–2008) with PbA data from the U.S. Environmental Protection Agency. We applied mixedeffects models, and we computed slope factor, d[PbB]/d[PbA] or the change in PbB per unit change in PbA, from the model results to assess the relationship between PbB and PbA.
Results: Comparing the NHANES regression results with those from the literature shows that slope factor increased with decreasing PbA among children 0–11 years of age.
Conclusion: These findings suggest that a larger relative public health benefit may be derived among children from decreases in PbA at low PbA exposures. Simultaneous declines in Pb from other sources, changes in PbA sampling uncertainties over time largely related to changes in the size distribution of Pbbearing particulate matter, and limitations regarding sampling size and exposure error may contribute to the variability in slope factor observed across peerreviewed studies.

Citation: RichmondBryant J, Meng Q, Davis A, Cohen J, Lu SE, Svendsgaard D, Brown JS, Tuttle L, Hubbard H, Rice J, Kirrane E, VinikoorImler LC, Kotchmar D, Hines EP, Ross M. 2014. The Influence of declining air lead levels on blood lead–air lead slope factors in children. Environ Health Perspect 122:754–760; http://dx.doi.org/10.1289/ehp.1307072
Address correspondence to Q. Meng, School of Public Health, Rutgers University, Piscataway, NJ 08854 USA. Telephone: (732) 2359754. Email: mengqi@sph.rutgers.edu
We give special thanks to T. Luben, Z. Pekar, R. Sams, and J. Vandenberg for their helpful comments in review of this manuscript; and we thank N. Kravets of the National Center for Health Statistics, Centers for Disease Control, for linking the NHANES (National Health and Nutrition Examination Study) data with the AQS (Air Quality System) data.
This research was supported by the U.S. Environmental Protection Agency (EPA). The research and this manuscript have been reviewed in accordance with U.S. EPA policy and approved for publication. Mention of trade names or commercial products does not constitute endorsement or recommendation for use. The views expressed in this article are those of the authors and do not necessarily reflect the views or policies of the U.S. EPA.
J.C. and H.H. are employed by ICF International, Fairfax, Virginia. The authors declare they have no actual or potential competing financial interests.
Received: 10 May 2013
Accepted: 24 March 2014
Advance Publication: 25 March 2014
Final Publication: 1 July 2014  Supplemental Material (227 KB) PDF
Introduction
Lead (Pb) in blood (PbB) reflects all sources and pathways of human exposure to Pb; hence, dramatic declines in PbB levels reported in the National Health and Nutrition Examination Survey (NHANES) have coincided with the phaseout of leaded gasoline and other regulatory restrictions on Pb in industry and consumer products (Brody et al. 1994; Pirkle et al. 1994, 1998). Current sources of Pb potentially contributing to Pb body burden include ambient sources such as some pistonengine aircraft fuel and Pbacid battery recycling operations, whereas nonambient sources include Pb in building materials used in older homes [U.S. Environmental Protection Agency (EPA) 2011]. Given the multitude of potential Pb sources and pathways of exposure, it is often difficult to distinguish the proportion of PbB attributed to airrelated pathways—those pathways where Pb passes through ambient air from a source to human exposure. Airrelated pathways include inhalation of airborne Pb (freshly emitted or resuspended) and ingestion of Pb that, once airborne, has made its way into indoor dust, outdoor dust or soil, dietary items, and drinking water.
Epidemiologic studies have explored the relationship between PbB and ambient air Pb (PbA) with regression or other statistical modeling techniques using individual or aggregated data (e.g., Brunekreef 1984; Hayes et al. 1994; Schwartz and Pitcher 1989; Tripathi et al. 2001). Statistical models typically have PbB as the dependent variable, and PbA is either the only independent variable or is adjusted by one or more covariates, such as race/ethnicity or home age. Model formulations have varied with respect to use of transformation functions (e.g., applying a logarithm to terms on one or both sides of the equation) and stratification of the sample population. As a result, pointwise estimation of the slope factor, or the change in PbB per unit change in PbA—d[PbB]/d[PbA]—has also varied between and within statistical models; in the latter case, withinmodel variation occurs for nonlinear formulations.
The overall objective of this work is to evaluate how the relationship between PbB levels in children and PbA levels has changed following the phaseout of leaded gasoline and tightened controls on environmental Pb emissions over the past 30 years. In this study we explored the relationship of PbB with PbA over the course of several papers that describe the statistical modeling techniques and results for effect estimates for PbA, calculate slope factor for different PbA size fractions, and investigate effect modification of the PbB–PbA relationship. The results presented here focus on the comparison of the slope factor results for PbA concentration data in total suspended particles (TSP) with results from studies in the literature performed between 1970 and 2011.
Methods
Data sets. RichmondBryant et al. (2013) provided a detailed description of the data sets used in this analysis, which is summarized briefly here. We obtained participantlevel data for this analysis from the NHANES III (1988–1994) and Continuous NHANES (1999–2008) (hereafter referred to as NHANES 9908) surveys [Centers for Disease Control and Prevention (CDC) 2014]. We obtained the NHANES data in 2year cycles. We also used the data imputation scheme described by RichmondBryant et al. (2013) for this data set to account for missing data, except for the PbB variable. When PbB was missing, we omitted the data record because it was the dependent variable. We stratified the data by age groups used in NHANES (1–5 years, 6–11 years) to reflect potential differences in Pb storage, Pb distribution, Pb metabolism, and handtomouth behavior among young and older children. However, we did not use other covariates in the analysis because the PbA thereby accounted for all airrelated pathways contributing to PbB (U.S. EPA 2013).
Air Quality System (AQS) data variables included TSP in PbA (TSPPbA) concentration, monitor identification number, latitude, longitude, and date. We used particulate matter (PM) sampled as TSP from a highvolume sampler for this analysis because other peerreviewed studies, to which these results were compared, employed TSPPbA. Roughly 270 TSP monitors for sampling PbA were active as of February 2010 (U.S. EPA 2008a). Over the course of NHANES 9908, 456 monitor locations corresponded to PbB data and collected 108,126 data points. During NHANES III, 756 monitor locations corresponded to PbB data and collected 178,036 data points. Samples were collected on a 24hr basis. Among those monitors reporting data acquisition frequency, 1.9% reported collected data each day, 0.2% every other day, 3.7% every third day, 83.5% every sixth day, 10.6% every twelfth day, and 0.2% every 30 days. On the basis of an anticipated 286,162 samples for the years of sampling at the frequencies listed above, we estimated 64% of 24hr data to be missing for NHANES 9908 and 26% of 24hr data to be missing for NHANES III. To be included in this study, we required 75% data completeness for monitors for the years in which the monitors were active. However, many of the TSPPbA monitors were not active for all years coinciding with NHANES III and NHANES 9908. We averaged PbA concentrations over 365 days before the PbB sample. We did not use PbA observations with missing and zero values of concentration in the analyses because the statistical model described below used a logarithmic transformation. However, we did not omit nonzero data below the method detection limit (MDL) for sampling and analysis of PbA, to minimize upward bias of the PbA data distribution. MDL was ≤ 0.002 μg/m^{3} for 60% of the monitors. MDL was ≤ 0.01 μg/m^{3} for 98% of the monitors, and for one monitor, MDL was 0.05 μg/m^{3}. For NHANES 9908, 23% of data averaged over 365 days were below MDL, and 3.8% of the data averaged over 365 days had zero values and hence were omitted. For NHANES III, 6.2% of the data averaged over 365 days were below MDL, and 1.5% of the data averaged over 365 days had zero values. Because the data were averaged over 365 days, we deemed data imputation unnecessary. However, we acknowledge that omission of data would induce uncertainty in the PbA distribution.
Data for PbA and PbB were merged into one database based on the NHANES participants’ location and date of examination. Staff at the National Center for Health Statistics Research Data Center (RDC) (CDC 2012) merged the data to maintain confidentiality of the NHANES participants’ personal data. When a TSPPbA monitor was located within 4 km of a census block–group centroid in which an NHANES participant resided and a 24hr TSPPbA concentration measurement fell within 7 days of the NHANES participant examination date, RDC staff assigned the 365day average TSPPbA concentration from that TSPPb sampler to that participant. We applied a 7day window for the data merger because the TSPPbA data were typically obtained every 6 days.
We selected the 4km buffer size based on the Code of Federal Regulations (U.S. EPA 1979a), which established microscale (100 m), middlescale (100–500 m), neighborhoodscale (within 4 km), urbanscale (10s of km), and regionalscale (100s of km) measurements all as potential buffers in which PbA concentration could be measured. Neighborhood scale is cited as representative of PbA concentrations in urban areas not near sources (U.S. EPA 1979b). Although the 4km neighborhood scale is somewhat arbitrary, it is well known that larger Pb particles tend to settle out, whereas smaller particles have the potential for longer transport (U.S. EPA 1979a).
After the data were merged, RDC staff deidentified the data set by removing geographic location and date fields before use of the database for analysis. The University of North Carolina Institutional Review Board (IRB) reviewed the study design and deemed it exempt from IRB oversight. RichmondBryant et al. (2013) detailed the data merge procedures briefly described here.
Statistical analysis. We employed a simplified univariate approach for this analysis to estimate the change in PbB in response to a change in PbA. Use of a univariate model enabled all airrelated pathways of Pb exposure to be incorporated into the one term for PbA, because covariates such as housing age could reflect exposure to deposited PbA. The detailed multilevel linear mixedeffects (LME) modeling approach is presented by RichmondBryant et al. (2013). PbA was a census block group–level fixed effect in the model. The random effects at the census block group level were random intercepts for each census block group identification number, and the residual error terms were random effects at the individual level. We treated subject age strata and NHANES survey (NHANES III or NHANES 9908) as stratification variables. We treated the geographical location as a random effect. The LME model was of the form
ln[PbB_{i,j}] = β_{0} + b_{j} + β_{PbA}ln[PbA_{j}] + ε_{i,j}, [1]
where PbB_{i,j} is the PbB for the ith individual living in the j th census block group, [PbA_{j}] is the average PbA concentration obtained at the jth census block group, and β_{PbA} is the slope of ln(PbB) on ln(PbA) for the jth census block group (and ln denotes the natural logarithm). β_{0} is the overall intercept, b_{j} is a census block group–level random normal intercept with mean zero and variance τ^{2}, and ε_{i,j} is a random normal variable with mean zero and variance σ^{2}. We performed likelihood ratio testing to test the statistical significance of ln(PbA) by running Equation 1 with and without the PbA variable. Because this model does not include demographic and other covariates, their potential effects on PbB are incorporated in the random census block–group effect and residual error terms. The model used by RichmondBryant et al. (2013) adds various demographic and covariate fixedeffect terms to the righthand side of Equation 1. We used simulations to evaluate the choice of the ln–ln model to fit the data, and we described the simulations in the Supplemental Material, “Simulation methods,” pp. 2–4, and Tables S1 and S2. We evaluated the simulated model results against each other and against the results of the model using the merged data set. We selected the ln–ln model fit to the simulated data as most similar to the model fit for the merged data sets. The RDC maintains a strict policy of prohibiting restrictedaccess NHANES data users to plot real data points with the regression curve or to output residuals, to avoid the possibility that an individual participant’s identity could be reconstructed by using their exposures as measured at the nearest monitor to find the participant’s approximate location and then to match the associated PbB level and covariates.
RabeHesketh and Skrondal (2006) have found that incorporation of survey weights in multilevel models using a pseudolikelihood approach can lead to biased estimates if the level1 weights are different from 1 and if the cluster sizes are small. For this reason, we did not apply sampling weights calculated for NHANES to adjust for oversampling segments of the population (e.g., for race/ethnicity, age group, or urbanization) in the LME analysis.
Computation of slope of PbB to PbA. We employed Equation 1 for computing the slope factors used to interpret the relationship between PbB and PbA. For this study, we derived an instantaneous slope factor, d[PbB]/d[PbA], for the ln–ln model in lieu of intervalbased approximations for slope used in earlier studies (e.g., Brunekreef 1984; Hayes et al. 1994):
d[PbB]/d[PbA] = e^{β0}β_{PbA}[PbA]^{β}^{PbA}^{–1}^{.} [2]
In addition to ensuring that the PbA term accounted for all airrelated pathways, use of Equation 1 allowed for straightforward calculation of the slope factor because calculation of slope factor with a covariate model would entail testing of several hypothetical scenarios to estimate covariate values. With a combination of categorical and continuous covariates, this step is not straightforward. Brunekreef (1984) recognized that computation of slope factor from a model not including covariates may result in some amplification of slope factor. We assumed that the average b_{j} over all census block groups was equal to zero, so the random intercept does not appear in Equation 2.
Literature review. We included studies computing slope factor that were presented by U.S. EPA (2013) for comparison with the NHANES analyses (Brunekreef 1984; Hayes et al. 1994; Hilts 2003; Schwartz and Pitcher 1989; Tripathi et al. 2001). To ensure that we did not miss additional relevant studies, we also conducted a Web of Science (http://thomsonreuters.com/thomsonreuterswebofscience/) search using the topic queries “blood Pb” and “air Pb.” We retrieved 162 articles from this search. We reviewed the titles and abstracts from these references to determine if the associations between PbB and PbA were studied in those articles. We reduced the pool of articles to 11 after the title–abstract review. We reviewed the 11 remaining articles in full, and only three new articles—Bierkens et al. (2011), Ranft et al. (2008), and Zahran et al. (2013)—included a statistical model of PbB as a function of PbA. For each of the statistical models presented in these eight studies, we computed slope factor based on Equation 2. If any study used base10 logarithms in lieu of natural logarithms, then we replaced the exponential with a base of 10 in Equation 2.
Results and Discussion
Regression results show that β_{PbA} decreased substantially between NHANES III and NHANES 9908, as shown in Table 1. For NHANES III, β_{PbA} was 0.140 (p = 0.011) for the 1 to 5year age group and 0.154 (p = 0.067) for the 6 to 11year age group. For NHANES 9908, β_{PbA} was 0.076 (p = 0.12) for the 1 to 5year age group and 0.155 (p = 0.0012) for the 6 to 11year age group. The magnitude of β_{PbA} for Equation 1 of NHANES 9908 was 54% and 101% of that for NHANES III for the 1 to 5year and 6 to 11year age groups, respectively. Likelihood testing produced the same findings with respect to statistical significance of ln(PbA) for both NHANES cycles and models. Figure 1 displays the modeled relationship between PbB and PbA for children 1–5 years of age based on the NHANES 9908 data. The ln–ln model design is evident from the steepness of the tangent slope factor for small PbA with a sharp decrease in slope factor with increasing PbA.
Table 1 – Regression coefficients (β ± SE) for merged PbB–PbA data set, based on annual average TSP‑Pb data.
Figure 1 – Calculated PbB levels for a range of PbA concentrations for the NHANES 9908 models for children 1–5 years of age. Tangent lines are shown in gray to illustrate how slope factor decreases with increasing PbA along the ln–ln model.
We observed little difference among the slope factors between NHANES III and NHANES 9908; this information is shown in Table 2 at the median concurrent PbA concentration. For NHANES III, slope factor was 16.4 μg/dL per μg/m^{3} for the 1 to 5year age group and 15.7 μg/dL per μg/m^{3} for the 6 to 11year age group at a median PbA of 0.036 μg/m^{3} and 0.037 μg/m^{3}, respectively; slope factor was statistically significantly greater than zero. For NHANES 9908, slope factor was also statistically significantly greater than zero. For the 1 to 5year and 6 to 11year groups, slope factor was 15.3 and 16.5 μg/dL per μg/m^{3} at PbA of 0.011 to 0.016 μg/m^{3}, respectively; these slope factor values were close to values calculated from the NHANES III simulations. Similarities in slope factor for the 1 to 5year and 6 to 11year age groups arose because differences between the models’ β_{PbA} and β_{0} among the NHANES survey cycles were offset by the reduction in PbA from 0.036 to 0.037 μg/m^{3} for the 1988–1994 survey down to 0.011 to 0.016 μg/m^{3} for the 1999–2008 survey. Given the complex structure of Equation 2, slope factor increases with decreasing PbA when β_{PbA} and β_{0} are fixed. Larger values for β_{0} and β_{PbA} will also result in higher slope factor. β_{0} and β_{PbA} for NHANES III were > 1.75 times higher than for NHANES 9908 in the 1 to 5year age group, and β_{0} was roughly 1.5 times higher in the 6 to 11year group for NHANES III compared with NHANES 9908.
We computed slope factors presented in the above paragraph with the fixedeffects slopes derived from the mixed models (Table 2). Additionally, we added a random effect to the intercept to account for the influence of geography on an individual’s slope factor in the LME model. Given that we added the random effect to the intercept, it would have the effect of multiplying slope factor by exp(b_{j}), such that Equation 2 would become
d[PbB]/d[PbA] = e^{β0}^{+bj}β_{PbA}[PbA]^{β}^{PbA}^{–1}^{.} [3]
The variance of the random effect, given in Table 1, was used to calculate how the slope factor would change over the 95% confidence interval of the random effect, by adding ±1.96[var(b_{j})/n]^{0.5} in place of b_{j} in Equation 3. This results in the slope factor being multiplied by a factor within the interval [0.93,1.07] to capture the influence of the random effect across the age groups and survey cycles.
We compared slope factors from the results of this study with those computed from related studies in the literature. Although many studies provided slope factor, we recomputed it here as the first derivative of the PbB–PbA regression relationship presented in each study to ensure that the computational approach was equivalent because some studies estimated slope factor based on interval approximation (e.g., Brunekreef 1984; Hayes et al. 1994). Additionally, we computed slope factor using the median PbA to maintain consistency among the models. For the ln–ln models, use of low current levels of PbA (e.g., for NHANES 9908, median PbA ranged from 0.011 to 0.016 μg/m^{3}) would drive slope factor upward compared with using PbA closer to 1 μg/m^{3} for older studies, because the ln–ln curves are steeper at lower PbA; this is evident in Figure 1. Linear models had constant slope factor, so that the relative difference in slope factor between the ln–ln and linear models increased with decreasing PbA.
Most studies of the PbB–PbA relationship employed data from the period when Pb was used as an antiknock agent in gasoline and a more prevalent raw material in manufactured goods in the United States and abroad (Brunekreef 1984; Hayes et al. 1994; Hilts 2003; Ranft et al. 2008; Schwartz and Pitcher 1989; Tripathi et al. 2001). We summarized these studies in Table 2 along with data from this study. We observed variability in the studies’ median slope factor estimates; Brunekreef (1984), in a metaanalysis of earlier studies associating PbB with PbA, also noted such variability. For the studies that obtained most data when industrial and automotive Pb usage was higher, slope factor ranged from 3.2 to 12.2 (Brunekreef 1984; Hayes et al. 1994; Hilts 2003; Ranft et al. 2008; Schwartz and Pitcher 1989; Tripathi et al. 2001). Bierkens et al.’s (2011) study of PbA exposure throughout the European Union (EU) included many data from after 2000, when EU countries had phased out Pb from automotive gasoline and saw diminished industrial use. They observed a slope factor of 2.8 μg/dL per μg/m^{3} among children 0–6 years of age. Likewise, Zahran et al.’s (2013) study of PbA exposure in Detroit, Michigan, used data from 2001–2009 and observed slope factor ranging from 17 to 63 μg/dL per microgram per cubic meter for children 0–10 years of age in 1 to 3year age groupings. The U.S. EPA (2007) reviewed the evidence before 2007 and determined that slope factor overall was between 3 and 10 μg/dL per μg/m^{3} (i.e., an increase in PbA concentration of 1 μg/m^{3} would translate to increases in PbB levels of 3–10 μg/dL).
Table 2 shows comparison of slope factor, computed at the studies’ median PbA among this and other studies modeling PbB as a function of PbA. All computed slope factors were statistically significant. Median slope factor across the 21 models presented in Table 2 for children 0–11 years of age was 16.4 μg/dL per μg/m^{3}. Slope factors across the studies had an interquartile range of 24.9 μg/dL per μg/m^{3}. Computations from the NHANES III and NHANES 9908 analyses and for Zahran et al. (2013) yielded higher slope factor than the other studies modeling PbB vs. PbA.
To explore potential reasons for higher slope factor values among children 0–11 years of age for the NHANES analyses and for Zahran et al. (2013) compared with the other studies in the literature, slope factor was plotted against median PbA for these studies (Figure 2). Here, the median PbA values (0.011–0.037 μg/m^{3}) for the four NHANES analyses and for the Zahran et al. (2013) study were substantially lower than median PbA for the other studies (0.098–2 μg/m^{3}). Hence, the study results taken in concert suggest that slope factor increases among children with decreasing exposure to PbA. This is consistent with the curve of PbB versus PbA presented in Figure 1 and with the inverse mathematical dependence of slope factor with PbA, as seen in Equation 2. The declining relationship between slope factor and PbA in ln–ln space supports use of the ln–ln plot to describe the relationship between PbB and PbA. Furthermore, examination of slope factor for many studies across a range of PbA lends additional credence to the notion that slope factor increases with decreasing PbA, as illustrated in Figure 3 for the PbB–PbA models computed from the studies of childhood exposure included here. In this sense, the decreased PbA concentrations for the NHANES and Zahran et al. (2013) studies account for higher slope factor observed in Figure 2. When PbA is already low, additional reduction in PbA would then produce a larger proportional decrease in PbB compared with the same reduction at a higher initial PbA. Variation in the β_{PbA} and β_{0} of the PbB–PbA curve causes some of these differences. For example, the curves from Brunekreef (1984) and Hayes et al. (1994) have much larger β_{PbA} compared with the other models. In other cases, the different model curves in Figure 3 illustrate that β_{PbA} of many of the models is similar, but β_{0} differs. These differences in β_{0} are likely responsible for the amount of scatter observed in Figure 2 among slope factor for higher PbA.
Figure 2 – Slope factor versus PbA for children 0–11 years of age, with slope factor computed for the median PbA at the time of the study. Data for the present study are shown with white circles.
Figure 3 – Calculated PbB levels for a range of PbA concentrations for all studies with study participants 0–11 years of age and using a ln–ln or log–log model of the PbB–PbA relationship.
The large amount of scatter in the graph of slope factor versus PbA presented in Figure 2 suggests variation in the form of the ln–ln relationship between PbB and PbA over the years 1970–2009. During this time period, several changes to population Pb exposure have occurred. By 2000, most countries had phased out Pb additives from gasoline, and the timing and duration of the phaseouts varied across the studies examined here. Additionally, environmental Pb emissions have decreased throughout the last 40 years (U.S. EPA 2008b). In a multivariate model using the NHANES III and NHANES 9908 data, the magnitude of ln(PbB) effect estimates varied between the NHANES cycles for socioeconomic and coexposure factors (RichmondBryant et al. 2013). Scatter in slope factor may also reflect differences in the covariates between the survey cycles.
This study is not without limitations. First, to preserve NHANES participant confidentiality, the RDC restricted printing or plotting the study data or residuals once the NHANES and AQS data sets were merged. As a result, visual inspection of the fit of the regression curves was not possible. Second, we used the 4km buffer size around the monitors to maintain the small distances likely travelled by Pb particles without losing excessive statistical power at the monitors. However, we lost some power, because application of the monitoring buffers caused reduction of the NHANES III sample population from 9,368 to 926; similarly, the NHANES 9908 sample population decreased from 8,244 to 409 after applying the buffers. Limiting the overall number of participants reduced the statistical significance of the study results. Stratifying the population by age and survey further reduced sample size. Third, use of the 4km buffers also potentially caused exposure misclassification, if PbA concentration was sometimes incorrectly assigned to an NHANES participant. We could not test other buffer sizes, because only RDC staff could perform the data merger. Fourth, selecting the centroid of the census block group in which the monitor resides as the comparison metric for the monitor location likely added exposure error because we did not know the proximity between the monitors and the individuals. Fifth, changes in PbA emissions from NHANES III to NHANES 9908 suggest that the size distribution of PbA particles would have changed, since Pb emitted to the air by automobiles were in the fine fraction; a recent review of the PbA literature supports this idea (Cho et al. 2011). This shift would change the amount of bias and uncertainty in PbA measurements, because errors in the PbA monitoring method increase with increasing particle size (Wedding et al. 1977). Additionally, larger particles are more likely to settle from the air compared with smaller particles (Fuchs 1964), so that a smaller fraction of the population may have been exposed to Pbbearing particles in 1999–2008 compared with 1988–1994. At the same time, the upward shift in size distribution of Pbbearing particles changes the site of deposition within the respiratory system, potentially increasing the amount of ingested versus inhaled Pb and related absorption (Niu et al. 2010). These two factors could have a real impact on slope factor. Sixth, the literature review within this current study used PbB–PbA data for distinct populations and analyzed by different models. Some of the trend and/or scatter might be attributed to those differences. Last, the results were not amenable to making national inference, because we did not apply the sample weights in the LME, as described in “Methods.” However, the study did sample a large crosssection of the United States. Except for Schwartz and Pitcher (1989), previous studies of the relationship between PbB and PbA in the United States were limited to specific cities. The limitations of the study are balanced by gaining an improved understanding of the PbB–PbA association for the period following the phase out of Pb as an antiknock agent in gasoline based on the linkage of two large databases.
Conclusions
The primary finding of this crosssectional epidemiologic study is that the slope factor increases with decreasing PbA for children 0–11 years of age, albeit with a large amount of scatter across the studies reviewed for comparison with the NHANES estimates. Because slope factor is higher at low PbA, larger relative PbB reductions among children may be achieved at low PbA levels. At the same time, we need more studies of the conditions influencing slope factor to interpret the results presented here. Additional analyses exploring the effect of particle size cuts for the PbA measurements and effect modification factors influencing slope factor are in progress.
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CEHN December 2014 Article of the Month
“The Navigation Guide—EvidenceBased Medicine Meets Environmental Health: Integration of Animal and Human Evidence for PFOA Effects on Fetal Growth” (Environ Health Perspect; DOI:10.1289/ehp.1307923) has been selected by the Children’s Environmental Health Network (CEHN) as its December 2014 Article of the Month. These CEHN summaries discuss the potential policy implications of current children’s environmental health research.
Introducing Children’s Health Collection 2014
EHP’s fifth annual Children’s Health Collection is now available. The collection comprises abstracts of all relevant articles published in EHP from October 2013 through September 2014: peerreviewed research articles, news features, Science Selections, and editorials.
ISEE 2014 Abstracts Now Available
EHP is pleased to present the abstracts for the 26th annual conference of the International Society for Environmental Epidemiology (ISEE), From Local to Global: Advancing Science for Policy in Environmental Health, held 24–28 August 2014 in Seattle, Washington.
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Recent Advance Publications

Autism Spectrum Disorder and Particulate Matter Air Pollution before, during, and after Pregnancy: A Nested Case–Control Analysis within the Nurses’ Health Study II Cohort

Comparative Effects of Di(nButyl) Phthalate Exposure on Fetal Germ Cell Development in the Rat and in Human Fetal Testis Xenografts

Interaction Effects of Temperature and Ozone on Lung Function and Markers of Systemic Inflammation, Coagulation, and Fibrinolysis: A Crossover Study of Healthy Young Volunteers

First Steps toward Harmonized Human Biomonitoring in Europe: Demonstration Project to Perform Human Biomonitoring on a European Scale

Children’s Health in Latin America: The Influence of Environmental Exposures