Component Description
Trace metals have been associated with adverse health effects in occupational studies or laboratory studies, but have not been monitored in general population groups.
This method is used to achieve rapid and accurate quantifications of multiple elements of toxicological and nutritional interest. The method is sensitive and rapid enough to screen urine specimens from subjects suspected to be exposed to a number of important toxic elements or to evaluate environmental or other nonoccupational exposure to these same elements.
Eligible Sample
Participants aged 6 years and older who met the subsample requirements.
Description of Laboratory Methodology
Inductively coupled plasma-mass spectrometry (ICP-MS) is a multi-element analytical technique (1). Liquid samples are introduced into the ICP through a nebulizer and spray chamber carried by a flowing argon stream. By coupling radio-frequency power into flowing argon, plasma is created in which the predominant species are positive argon ions and electrons. The sample passes through a region of the plasma that has a temperature of 6000–8000 K. The thermal energy atomizes the sample and then ionizes the atoms. The ions, along with the argon, enter the mass spectrometer through an interface that separates the ICP from the mass spectrometer, which is operating at an atmospheric pressure of 10–5 torr. The mass spectrometer permits ions at each mass to be detected in rapid sequence, allowing individual isotopes of an element to be determined. Electrical signals resulting from the detection of the ions are processed into digital information that is used to indicate first the intensity of the ions and then the concentration of the element. The ICP-MS method is used to measure the following 12 elements in urine: beryllium (Be), cobalt (Co), molybdenum (Mo), cadmium (Cd), antimony (Sb), cesium (Cs), barium (Ba), tungsten (W), platinum (Pt), thallium (TI), lead (Pb), and uranium (U). This method is based on the method by Mulligan et al. (2) Urine samples are diluted 1+9 with 2% (v/v), double-distilled, concentrated nitric acid containing both iridium (Ir) and rhodium (Rh) for multi-internal standardization. This procedure can be used for all 12 elements or subsets of the 12 elements.
Laboratory Quality Assurance and Monitoring
Urine specimens are processed, stored, and shipped to the Division of Environmental Health Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention for analysis.
Detailed specimen collection and processing instructions are discussed in the NHANES Laboratory/Medical Technologists Procedures Manual (LPM). Vials are stored under appropriate frozen (–20°C) conditions until they are shipped to National Center for Environmental Health for testing.
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.
The NHANES QA/QC protocols meet the 1988 Clinical Laboratory Improvement Amendments mandates. Detailed QA/QC instructions are discussed in the NHANES LPM.
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 2.0% of all specimens.
NCHS developed and distributed a quality control protocol for all the contract laboratories which outlined the Westgard rules used 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 and Westat 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 Science’s quality control and quality assurance performance criteria for accuracy and precision (similar to specifications outlined by Westgard 1981).
Analytic Notes
Subsample weights
Measures of urinary heavy metals were measured in a one third subsample of persons 6 years and over. 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.
Variance estimation
The analysis of NHANES 2003-2004 laboratory data must be conducted with the key survey design and basic demographic variables. The NHANES 2003-2004 Demographic Data File contains demographic and 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.
Links to NHANES Data Files
This laboratory data file can be linked to the other NHANES 2003-2004 data files using the unique survey participant identifier SEQN.
Detection Limits
The detection limit was variable for many of the analytes in the data set. Two variables are provided for each of these analytes. The variable named LBD___LC indicates whether the result was below the limit of detection. There are two values: “0” and “1”. “0” means that the result was at or above the limit of detection. “1” indicates that the result was below the limit of detection. Urinary beryllium, cadmium, lead, platinum, tungsten, and uranium have multiple lower limits of detection in this data file. The other variable named LBX___ provides the analytic result for that analyte. 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 two.
URXUCD and URDUCD:
When comparing urine cadmium across two-year cycles please note that even though these two variables have different names the data is comparable. Variable URXUCD is used in 1999-2000 and 2003-2004 and variable URDUCD was used in 2001-2002. Variable URDUCD was derived to correct for molybdenum interference (Reference to 2001-2002 lab 6 heavy metal documentation). Beginning in 2003-2004 the urinary cadmium data is corrected at the testing laboratory for molybdenum interference.
Please refer to the Analytic Guidelines for further details on the use of sample weights and other analytic issues.