• Component Description
• Eligible Sample
• Description of Laboratory Methodology
• Laboratory Method Files
• Laboratory Quality Assurance and Monitoring
• Data Processing and Editing
• Analytic Notes
• References
• Codebook
  • SEQN - Respondent sequence number
  • WTSC2YR - Environmental Subsample C Weights
  • URXUCR - Creatinine, urine (mg/dL)
  • URXDEE - DEET (ug/L)
  • URDDEELC - DEET comment code
  • URXDEA - DEET acid (ug/L)
  • URDDEALC - DEET acid comment code
  • URXDHD - Desethyl hydroxy DEET (ug/L)
  • URDDHDLC - Desethyl hydroxy DEET Comment Code

National Health and Nutrition Examination Survey

2013-2014 Data Documentation, Codebook, and Frequencies

DEET and Metabolites (DEET_H)

Data File: DEET_H.xpt

First Published: March 2017

Last Revised: NA

Component Description

DEET is a widely used insect repellent, sometimes combined with sunscreen agents and available for use in concentrations ranging from 4 to 100%. Human exposure may occur when DEET is absorbed through the skin or inhaled from aerosol formulations. Because DEET is widely used in the U.S. population, measuring urinary DEET and its metabolites is important to evaluate human exposure and potential for health effects.

N,N-diethyl-3-methylbenzamide, commonly known as DEET, is the principal ingredient in many personal insect repellents worldwide and is highly effective against a broad spectrum of insect pests, including potential disease vectors such as mosquitoes, biting flies and ticks (including many ticks that may carry Lyme disease).

DEET was first developed and patented in 1946 by the U.S. Army for use by military personnel and later registered for general public use in 1975. Every year, approximately one-third of the U.S. population uses DEET-containing insect repellent products with concentrations ranging from 10 to 100% in a variety of liquids, lotions, gels, sprays, sticks and impregnated materials and more than 30 million packages of DEET-containing products are sold annually. Approximately 230 products containing DEET are registered with the Environmental Protection Agency by about 70 different companies.

Although the clinical relevance of this method, on rare occasions, may extend to quantifying concentrations for emergency responses, such as accidental poisonings, its design and intended use is to provide data in support of epidemiological studies. It does not directly test for any disease.

Eligible Sample

Examined participants aged 6 years and older from a one-third sample were eligible.

Description of Laboratory Methodology

This method uses online solid phase extraction coupled with high performance liquid chromatography-tandem mass spectrometry (SPE-HPLC-MS/MS) for quantifying DEET and two of its metabolites, N,N-diethyl-3-hydroxymethylbenzamide (DHMB) and 3-diethyl-carbamoyl benzoic acid (DCBA), in 100 µL of human urine. Sample preparation begins with an over-night enzymatic deconjugation of the glucuronide-bound metabolites. On the second day, the four compounds being measured are concentrated via online SPE and then chromatographically separated from each other and from other urine biomolecules using reversed phase HPLC. The eluting molecular ions are converted to gas phase ions using Atmospheric Pressure Chemical Ionization (APCI) and then selectively filtered by mass-to-charge ratios at unit resolution. Select molecular ions are then fragmented with collision induced dissociation (CID) and the resulting product ions are filtered at unit resolution before detection via an electron multiplier.

Refer to the Laboratory Method Files section for detailed laboratory procedure manual(s) of the methods used.

There were no changes to the lab method, lab equipment, or lab site for this component in the NHANES 2013-2014 cycle.

Laboratory Method Files

N,N-diethyl-3-methylbenzamide, N,N-diethyl-3-hydroxymethylbenzamide, and 3-diethyl-carbamoyl benzoic acid (March 2017)

Laboratory Quality Assurance and Monitoring

Urine specimens are 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 specimen collection and processing instructions are discussed in the NHANES Laboratory Procedures Manual (LPM). Vials are stored under appropriate frozen (-20°C) conditions until they are shipped to National Center for Environmental Health for testing.

The NHANES quality assurance and quality control (QA/QC) protocols meet the 1988 Clinical Laboratory Improvement Amendments 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 quality assurance evaluation during unscheduled visits to evaluate both the quality of the laboratory work and the quality-control procedures. Each laboratory staff person is observed for equipment operation, specimen collection and preparation; testing procedures and constructive feedback are given to each staff. 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 on “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 the 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 Environmental Health 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

Subsample weights

DEET and metabolites were measured in a one third subsample of persons 6 years and 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.

Demographic and Other Related Variables

The analysis of NHANES laboratory data must be conducted using the appropriate survey design and demographic variables. The NHANES Demographic Data 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.

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

Detection Limits

The detection limits were constant for all of the analytes in the data set. Two variables are provided for each of these analytes. The variable name ending in “LC” (ex., URDDEELC indicates whether the result was below the limit of detection. The value “0” means that the result was at or above the limit of detection, “1” indicates that the result was below the limit of detection. For analytes with analytic results below the lower limit of detection (i.e., URDDEELC=1), an imputed fill value was placed in the analyte results field. This value is the lower limit of detection divided by square root of 2 (LLOD/sqrt [2]).

The other variable prefixed URX (ex., URXDEE) provides the analytic result for that analyte.

The lower limit of detection (LLOD in ug/L) for DEET and its metabolites are:

Variable Name	SAS Label	LLOD
URXDEE	N,N-diethyl-meta-toluamide (DEET) (ug/L)	0.0830
URXDEA	DEET acid (ug/L)	0.4750
URXDHD	N,N-Desethyl hydroxy benzmde DEET (ug/L)	0.0890

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

 

References

• Caudill, S.P., Schleicher, R.L., Pirkle, J.L. Multi-rule quality control for the age-related eye disease study. Statist. Med. (2008) 27(20):4094-40106.
• Westgard J.O., Barry P.L., Hunt M.R. Clin Chem (1981) 493.

Codebook and Frequencies