Title: Vitamin B6
Contact Number: 1-866-441-NCHS
Years of Content: 2003 - 2004
First Published: February, 2007
Access Constraints: None
Use Constraints: None
Geographic Coverage: National
Record Source: NHANES 2003 - 2004
Survey Methodology: NHANES 2003 - 2004 is a stratified multistage probability sample of the civilian non-institutionalized population of the U.S.
Medium: NHANES Web site; SAS transport files
The objectives of this component are:
These data will be used to estimate deficiencies and toxicities of specific nutrients in the population and subgroups, to provide population reference data, and to estimate the contribution of diet, supplements, and other factors to serum levels of nutrients. Data will be used for research to further define nutrient requirements as well as optimal levels for disease prevention and health promotion.
Participants aged 1 year and older were tested.
Pyridoxal 5’- phosphate (PLP) is the biologically active form of the vitamin B6. Vitamin B6 is involved in numerous metabolic pathways as an enzyme cofactor. Homocysteine (HCY), a risk factor for cardiovascular and other diseases, is converted to cysteine by PLP-dependent transsulfuration enzymes. A major cause of homocysteinemia is insufficient intake of vitamin B6, vitamin B12, and folic acid, all of which are also necessary for HCY metabolism. Clinical studies suggest that vitamin B6 is independently associated with increased risk for cardiovascular disease. Recent studies have shown that plasma PLP levels are significantly decreased in other pathological conditions, including rheumatoid arthritis. High tHcy and low vitamin B6 plasma levels are associated with an increased risk for deep venous thrombosis (DVT) independent of other established risk factors for DVT. The association of low vitamin B6 levels with the risk for DVT is also independent of the tHCY levels. Testing for Vitamin B6 (Pyridoxal 5'-phosphate) began in 2003.
A detailed description of the laboratory procedures can be found at the NHANES web site.
Specimens were processed, stored and shipped to the AntiCancer, Inc. in San Diego, California. Detailed specimen collection and processing instructions was discussed in the NHANES LPM. Read the LABDOC file for detailed data processing and editing protocols. The analytical methods were described in the Description of the Laboratory Methodology section.
There was no top coding in this file.
Detailed instructions on specimen collection and processing can be found at NHANES web site.
The NHANES quality control and quality assurance protocols (QA/QC) meet the 1988 Clinical Laboratory Improvement Act mandates. A detailed quality control and quality assurance instruction was discussed in the NHANES Laboratory/Medical Technologists Procedures Manual (LPM). Read the LABDOC file for detailed QA/QC protocols.
A detailed description of the quality assurance and quality control procedures can be found at the NHANES web site.
The analysis of NHANES 2003-2004 laboratory data must be conducted with the key survey design and basic demographic variables. The NHANES 2003-2004 Household Questionnaire Data Files contain demographic data, health indicators, and other related information collected during household interviews. They also contain all survey design variables and sample weights for these age groups. The phlebotomy file includes auxiliary information such as the conditions precluding venipuncture. The household questionnaire and phlebotomy files may be linked to the laboratory data file using the unique survey participant identifier SEQN.
Please refer to the Analytic Guidelines for further details on the use of sample weights.
|Code or Value||Value Description||Count||Cumulative||Skip to Item|
|10 to 962||Range of Values||6862||6862|
|7.1||Fill Value of Limit of Detection||960||7822|