• Component Description
• Eligible Sample
• Description of Laboratory Methodology
• Laboratory Quality Assurance and Monitoring
• Data Processing and Editing
• Analytic Notes
• References
• Codebook
  • SAMPLEID - Pool identification number
  • RIAGENDR - Gender
  • ETHNICTY - Ethnicity - Recode
  • RIDAGGRP - Age group
  • RIANSMP - Number of samples in a pool
  • WTSMSMPA - Adjust sum sampling weights in same pool
  • LBCBB1 - 2,2',4,4',5,5'-hexabromobiphenyl (pg/g)
  • LBCBB1LA - 2,2',4,4',5,5'-hxbrmbiphl lipd adj(ng/g)
  • LBDBB1LC - 2,2',4,4',5,5'-hexabromobiphenyl comnt
  • LBCBR1 - 2,2',4-tribromodiphenyl ether (pg/g)
  • LBCBR1LA - 2,2',4-tribromodiphl ether lpd adj(ng/g)
  • LBDBR1LC - 2,2',4-tribromodiphenyl ether comment
  • LBCBR11 - PBDE 209 (pg/g)
  • LBCBR11L - PBDE 209 lipid adj (ng/g)
  • LBDBR11C - PBDE 209 comment
  • LBCBR2 - 2,4,4'-tribromodiphenyl ether (pg/g)
  • LBCBR2LA - 2,4,4'-tribrmdphenyl ether lpd adj(ng/g)
  • LBDBR2LC - 2,4,4'-tribromodiphenyl ether comment
  • LBCBR3 - 2,2',4,4'-tetrabromodiphenyl ether(pg/g)
  • LBCBR3LA - 2,2',4,4'-tetrmdiphnyl ethr lpd ad(ng/g)
  • LBDBR3LC - 2,2',4,4'-tetrabromphenyl ether comment
  • LBCBR4 - 2,2',3,4,4'-pentbromodiphnyl ether(pg/g)
  • LBCBR4LA - 2,2',3,4,4'-pentabromphnyl lpd adj(ng/g)
  • LBDBR4LC - 2,2',3,4,4'-pentabromphenyl ether comt
  • LBCBR5 - 2,2',4,4',5-pentabromodiphnyl ethr(pg/g)
  • LBCBR5LA - 2,2',4,4',5-pentabrompheyl lpd adj(ng/g)
  • LBDBR5LC - 2,2',4,4',5-pentabromphenyl ether comt
  • LBCBR6 - 2,2',4,4',6-pentabromodiphyl ether(pg/g)
  • LBCBR6LA - 2,2',4,4',6-pentabromdphyl lpd adj(ng/g)
  • LBDBR6LC - 2,2',4,4',6-pentabromdphenyl ether comt
  • LBCBR66 - 2,3',4,4'-tetrabromodiphenyl ether(pg/g)
  • LBCBR66L - 2,3',4,4'-tetrabromodiphyl lpd adj(ng/g)
  • LBDBR66C - 2,3',4,4'-tetrabromodiphenyl ether comt
  • LBCBR7 - 2,2',4,4',5,5'-hxbromodiphnyl ethr(pg/g)
  • LBCBR7LA - 2,2',4,4',5,5'-hxbrompheyl lpd adj(ng/g)
  • LBDBR7LC - 2,2',4,4',5,5'-hexabromphenyl ether comt
  • LBCBR8 - 2,2',4,4',5,6'hexabromodiphyl ethr(pg/g)
  • LBCBR8LA - 2,2',4,4',5,6'-hxabromphyl lpd adj(ng/g)
  • LBDBR8LC - 2,2',4,4',5,6'-hexabromphenyl ether comt
  • LBCBR9 - 2,2',3,4,4',5,6heptbromdiphyl ethr(pg/g)
  • LBCBR9LA - 2,2',3,4,4',5',6-heptbrphl lpd adj(ng/g)
  • LBDBR9LC - 2,2',3,4,4',5',6-heptabrophenl ether cmt

National Health and Nutrition Examination Survey

2005-2006 Data Documentation, Codebook, and Frequencies

Brominated Flame Retardants (BFRs) - Pooled Samples (BFRPOL_D)

Data File: BFRPOL_D.xpt

First Published: July 2013

Last Revised: November 2020

Component Description

Polybrominated diphenyl ethers (PBDEs) and 2,2’,4,4’,5,5’-hexabromobiphenyl (PBB-153) are included in a larger group of chemicals known as brominated flame retardants (BFRs) that are added to products such as foam padding, textiles, or plastics to prevent accidental ignition and fire development. BFRs are not chemically bound to the flame-retarded material, so they can enter the environment from volatilization, leaching, or degradation of BFR-containing products. PBDEs are generally persistent in the environment and have been measured in aquatic sediments, house dust, and aquatic and terrestrial animals. PBDEs have been shown to bio accumulate in fish. Humans may be exposed though the diet, including breast feeding, and by contact with BFR-treated products and contaminated house dust.

Eligible Sample

Examined participants aged 12 years and older from a one-third subsample were eligible.

Description of Laboratory Methodology

Eleven polybrominated diphenyl ethers (PBDEs) and PBB-153 were measured in serum through the use of automated liquid/liquid extraction and subsequent sample clean-up. Final determination of target analytes wasperformed by isotope dilution gas chromatography high-resolution mass spectrometry GC/IDHRMS. The analytical method is described in Jones et al, 2012, which is a modification of the method described by Sjodin et al., 2004.

Refer to the Laboratory Methods Files section for a detailed description of the laboratory methods used.

There were no changes to the lab method, lab equipment, or lab site for this component in the NHANES 2005-2006 cycle. However, the samples were measured in a pooled fashion for 2005-2006 rather than individual measurements.

Laboratory Quality Assurance and Monitoring

Serum samples were processed, stored and shipped to the Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA for analysis. 

Detailed instructions on specimen collection and processing are discussed in the NHANES Laboratory Procedure Manual (LPM). Vials are stored under appropriate frozen (-30^oC) conditions until they were shipped to the National Center for Environmental Health for testing. 

The NHANES quality assurance and quality control (QA/QC) protocols meet the 1988 Clinical Laboratory Improvement Act mandates. Detailed QA/QC instructions are discussed in the NHANES LPM.

Mobile Examination Centers (MECs)

Laboratory team performance is monitored using several techniques. NCHS and contract consultants use a structured competency assessment evaluation during visits to evaluate both the quality of the laboratory work and the quality-control procedures. Each laboratory staff member is observed for equipment operation, specimen collection and preparation; testing procedures and constructive feedback are given to each staff member. Formal retraining sessions are conducted annually to ensure that required skill levels were maintained.

Analytical Laboratories

NHANES uses several methods to monitor the quality of the analyses performed by the contract laboratories. In the MEC, these methods include performing blind split samples collected during “dry run” sessions. In addition, contract laboratories randomly perform repeat testing on 2% of all specimens.

NCHS developed and distributed a quality control protocol for all CDC and contract laboratories, which outlined the use of Westgard rules (Westgard, et al. 1981) when running NHANES specimens. Progress reports containing any problems encountered during shipping or receipt of specimens, summary statistics for each control pool, QC graphs, instrument calibration, reagents, and any special considerations are submitted to NCHS quarterly. The reports are reviewed for trends or shifts in the data. The laboratories are required to explain any identified areas of concern.

All QC procedures recommended by the manufacturers were followed. Reported results for all assays meet the Division of Laboratory Sciences’ quality control and quality assurance performance criteria for accuracy and precision, similar to the Westgard rules (Caudill, et al. 2008).

Data Processing and Editing

The data were reviewed. Incomplete data or improbable values were sent to the performing laboratory for confirmation.

Analytic Notes

Refer to the 2005-2006 Laboratory Data Overview for general information on NHANES laboratory data.

Please refer to the NHANES Analytic Guidelines and the on-line NHANES Tutorial for details on the use of sample weights and analytic issues.

Subsample Weights

The original pooled-sample weight created for this file released in July 2013 was not correctly stratified to the U.S population total. This new file contains the corrected sample weight (WTSMSMPA). No changes or corrections were made to the lab analyte data in this new release. Any analyses of the data using the old public use data file should be repeated using the corrected sample weight on this file.

BFR including PBDEs and PBB-153 were measured in a one-third subsample of participants 12 years older.  Special sample weights are required to analyze these data properly. Specific sample weights for this subsample are included in this data file and should be used when analyzing these data. Samples were pooled in groups of 8 samples per pool within 40 demographic groups. The analysis of NHANES 2005-2006 pooled-sample data must be conducted with the basic demographic variables provided in this data file. This pooled-sample data file cannot be linked to other NHANES 2005-2006 data. Because each sample person does not have an equal probability of selection, sample weighting is needed to produce correct population estimates of means, percentiles, and other descriptive statistics.

The pooled-sample weights required to produce estimates from these data are included in this data file.  The analysis of pooled-samples from survey data is a relatively new field of study, and there is currently no established method to produce variance estimates for these pooled results.   These data cannot be analyzed using software designed for complex surveys because design features are not available. 

Demographic and Other Related Variables

The analysis of NHANES laboratory data must be conducted using the appropriate survey design and demographic variables. The NHANES 2005-2006 Demographics File contains demographic data, health indicators, and other related information collected during household interviews as well as the sample design variables. The recommended procedure for variance estimation requires use of stratum and PSU variables (SDMVSTRA and SDMVPSU, respectively) in the demographic data file.

The Fasting Questionnaire File includes auxiliary information, such as fasting status, length of fast and the time of venipuncture.

This laboratory data file can be linked to the other NHANES data files using the unique survey participant identifier (i.e., SEQN).

Rationale and Methods Used to Create Pooled Results

The Centers for Disease Control and Prevention (CDC) provide an ongoing assessment of the US population's exposure to environmental chemicals by using biomonitoring in conjunction with CDC's National Health and Nutrition Examination Survey (NHANES). Characterizing the distributions of concentrations of environmental compounds or their metabolites in the US population is a primary objective of CDC's biomonitoring program. Historically, this characterization has been based on individual measurements of these compounds in body fluid or tissue from representative samples of the population. Pooling samples allows for larger sample volumes, which can result in lower limits of detection and reduces the number of measurements and costs. For the first time in NHANES 2005-2006, a weighted pooled-sample design was implemented to facilitate pooling samples before making analytical measurements (pooled results were not weighted in NHANES 2001-2002). Table 1 lists the IUPAC (International Union of Pure and Applied Chemistry (IUPAC) names, common abbreviation, and NHANES variable name for the analytes included in this data file.

Pools were prepared from serum collected from a random one-third subset of the NHANES 2005–2006 participants aged 12 years and older. Samples were pooled based on gender, race and Hispanic origin, and age. To implement the pooled-sample design, each participant sample was identified as belonging to one of 32 demographic groups based on race and Hispanic origin (non-Hispanic white: NHW, non-Hispanic black: NHB, Mexican American: MA,: not non-Hispanic black, non-Hispanic white or Mexican-American: OTHER), gender (Male, Female), and age group (12-19, 20-39, 40-59, and 60+ years of age and older). Eight (8) samples were included in each pool. The number of pools created for each of the 32 demographic groups varied depending on the total number of individual samples available in a demographic group. The one-third subset of NHANES 2005-2006 represents 2345 individual samples, but because the pooled-sample design requires that all samples be of sufficient volume and that there be the same number of samples in each pool, only 1973 samples were available to create 247 pools with 8 samples per pool.  See more details on pool sample formation and exceptions in Table 2. The variable SAMPLEID denotes the identification number for each pool and ranges from 1 through 247. Please refer to the Pooled-Sample Technical Support file (POOLTF_D) for detailed information on individual participants included in each pool.

In order to incorporate sample weighting into the pooled-sample design it was necessary to use a different volume of material from each sample contributing to a pool. The volume chosen for each sample in a pool was based on the ratio of its sampling weight to the sum of the sampling weights of all samples in the pool. To physically accomplish the pooling in the laboratory required that the ratio of the largest to the smallest sampling weight of samples in the same pool be no larger than about 4 or 5. The individual samples were sorted/stratified by sampling weight within each of the 32 demographic groups and pools were formed using samples with sampling weights adjacent to one another in the sorted list. The number of samples in the one-third subset, the number of samples available, the number of these samples that were usable, and the number of pools formed in each demographic group are presented in Table 2. Once the pools were created, summed sampling weights were further adjusted to account for the unused samples. These adjusted summed sampling weights are represented by the variable named WTSMSMPA.

Detection Limits

In the dataset, the whole weight detection limit (pg/g serum) is a variable and dependent on the available sample size, however, the variation in sample size was low. Lipid adjusted detection limits are variable (ng/g lipid) due to differences of the lipid levels measured in individual pools/specimens. In cases where the result was below the limit of detection, the value for that variable is the detection limit divided by the square root of 2.

Table 1. NHANES Variable name, common abbreviation and International Union of Pure and Applied Chemistry (IUPAC) name for each analyte reported and maximum limit of detection (MLOD).

Variable	Common	IUPAC Name	MLODa
Name	Abbrev.		pg/g serum	ng/g lipid
LBCBR1	PBDE17	2,2´,4- Tribromodiphenyl ether	1.8	0.4
LBCBR2	PBDE28	2,4,4´-Tribromodiphenyl ether	1.8	0.4
LBCBR3	PBDE47	2,2´,4,4´-Tetrabromodiphenyl ether	1.8	0.4
LBCBR66	PBDE66	2,3´,4´,4-Tetrabromodiphenyl ether	1.8	0.4
LBCBR4	PBDE85	2,2´,3,4,4´-Tentabromodiphenyl ether	1.8	0.4
LBCBR5	PBDE99	2,2´,4,4´,5-Pentabromodiphenyl ether	1.8	0.4
LBCBR6	PBDE100	2,2´,4,4´,6-Pentabromodiphenyl ether	1.8	0.4
LBCBR7	PBDE153	2,2´,4,4´,5,5´-Hexabromodiphenyl ether	1.8	0.4
LBCBR8	PBDE154	2,2´,4,4´,5,6´-Hexabromodiphenyl ether	1.8	0.4
LBCBR9	PBDE183	2,2´,3,4,4´,5´,6-Heptabromodiphenyl ether	1.8	0.4
LBCBR11	PBDE209	Decabromodiphenyl ether	18	4.1
LBCBB1	PBB153	2,2´,4,4´,5,5´-Hexabromobiphenyl	1.8	0.4

^aThe values given in the tables are the maximum limit of detection (MLOD) divided by the square root of 2 and are expressed as pg/g serum and ng/g lipid.

 

Table 2.  Number of subjects per demographic group in the NHANES 2005–2006 one-third subsample, number of individual serum samples available, number of usable samples, and number of pools formed from usable samples. 

        
        ¹ Value of this categorical variable in the data set.
        ² With only 23 usable samples, two 8 sample pools and one 7 sample pool were created.
        ³ With only 6 usable samples, one 6 sample pool was created.

 

Methodological Considerations for analysis

There are a few pooled-sample methodological publications, which address issues related to the following topics (See References.)

• Variance estimation and bias correction when pooling samples from log-normally distributed populations (Caudill, 2010a; Caudill, 2010b; Caudill et al., 2007);
• Models that incorporate measurement error when analyzing pooled-samples from normally or log-normally distributed populations (Caudill, 2010a);
• Incorporation of sample weighting into a pooled-sample design (Caudill, 2012; Caudill, 2010a);
• Estimation of standard errors and confidence limits for point estimates from pooled-samples (Caudill, 2012; Caudill, 2010a). 

References

• Caudill SP, Characterizing populations of individuals using pooled samples. J Expo Sci Environ Epidemiol 2010a;20(1):29-37.
• Caudill SP, Important issues related to using pooled samples for environmental chemical biomonitoring. Stat Med 2010b;30(5):515-21.
• Caudill SP, Turner WE, and Patterson Jr. DG. Geometric mean estimation from pooled samples. Chemosphere 2007;69:371-80.
• Caudill SP, Use of pooled samples from the National Health and Nutrition Examination Survey. Stat Med 2012;31(27):3269-77.
  
• Jones R, Edenfield E, Anderson S, Zhang Y, Sjödin A. Semi-automated extraction and cleanup method for measuring persistent organic pollutants in human serum. Organohalogen Compounds 2012;A3:103. [online] available at: https://www.scienceopen.com/document?vid=9f9feb53-fd7e-4405-8cc1-18c162f9d1c7.
• Sjodin A, Jones RS, Lapeza CR, Focant J-F, McGahee EE III, Patterson DG Jr. Semiautomated high-throughput extraction and cleanup method for the measurement of polybrominated diphenyl ethers, polybrominated biphenyls, and polychlorinated biphenyls in human serum. Anal. Chem. 2004; 76:1921-7.
• Westgard JO, Barry PL, Hunt MR, Groth T. A multi-rule Shewhart chart for quality control in clinical chemistry. Clin Chem 1981;27(3):493-501.

Codebook and Frequencies