Among children ages 6-19 years who participated in NHANES between 2007 and 2008 and had stored serum samples available, Epstein-Barr virus (EBV) antibody testing was conducted. EBV VCA IgG antibody was measured using a commercial enzyme immunoassay kit.
Surplus sera from children aged 6 to 19 years who participated in NHANES years 2007 to 2008.
25 μL of sample is required for each assay. Specimens, calibrators and controls are pre-diluted 1:21 prior to placing them in the test wells. Cut-off calibrator, controls and subject samples are diluted according to the specific test kit protocol, mixed briefly by vortex to assure good distribution of the sample in the diluent, and then transferred to the appropriately labeled wells and incubated. After washing the wells, conjugate is added with another incubation and wash step following. Substrate is added and allowed to incubate before the addition of stop/color reagent. The plates are read at an absorbance of 450 nm using a reference wavelength of 630 nm. EIA indices are calculated by hand using the formulas in the kit package insert. Data are recorded (1) as Positive (EIA index ≥ 1.10), Negative (EIA index <0.90), or Equivocal (EIA index ≥ 0.90 to 1.09), and (2) as the exact numeric EIA index. The sensitivity of the assay is 96.6% and the specificity is 97.7%.
Data were submitted after all the antibody testing was complete. The data were not edited.
Commercial reagents were used for the EBV VCA IgG EIA antibody testing. All QA/QC procedures recommended by the manufacturer were followed.
The EIA indices have 4 categorical interpretations.
1. Negative. These samples have an EIA index <0.90.
2. Positive. These samples have an EIA index ≥1.10.
3. Equivocal. These samples have an EIA index ≥ 0.90 to 1.099.*
4. QNS. Quantity insufficient for testing. These samples were assigned an arbitrary index of missing.
*The only way to be certain if subjects with equivocal EIA antibody indices have been infected with EBV is to obtain another specimen from them. Since this is not practical and since this group is only a small fraction of the subjects tested (~0.05%), the cleanest approach to analyzing the data is to exclude them.
Subsample Weights
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. When observations were removed from this data file, a new sample weight was created and added to this data file (WTSSEB2Y). 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.
Code or Value | Value Description | Count | Cumulative | Skip to Item |
---|---|---|---|---|
6744.330171 to 131113.34923 | Range of Values | 1844 | 1844 | |
0 | No lab specimen | 0 | 1844 | |
. | Missing | 0 | 1844 |
Code or Value | Value Description | Count | Cumulative | Skip to Item |
---|---|---|---|---|
1 | Positive | 1371 | 1371 | |
2 | Negative | 459 | 1830 | |
3 | Equivocal | 13 | 1843 | |
4 | Quantity not sufficient | 1 | 1844 | |
. | Missing | 0 | 1844 |
Code or Value | Value Description | Count | Cumulative | Skip to Item |
---|---|---|---|---|
0.01 to 7.17 | Range of Values | 1843 | 1843 | |
. | Missing | 1 | 1844 |