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. 2009 May;117(5):784-9.
doi: 10.1289/ehp.0800376. Epub 2009 Jan 28.

Bisphenol A data in NHANES suggest longer than expected half-life, substantial nonfood exposure, or both

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Bisphenol A data in NHANES suggest longer than expected half-life, substantial nonfood exposure, or both

Richard W Stahlhut et al. Environ Health Perspect. 2009 May.

Abstract

Background: It is commonly stated in the literature on human exposure to bisphenol A (BPA) that food is the predominant BPA exposure source, and that BPA is rapidly and completely cleared from the body. If this is correct, BPA levels in fasting individuals should decrease with increased fasting time.

Objectives: We set out to investigate the relationship between urine BPA concentration and fasting time in a population-based sample.

Methods: We modeled log BPA urine concentration as a function of fasting time, adjusted for urine creatinine and other confounders, in 1,469 adult participants in the 2003-2004 National Health and Nutrition Examination Survey. We estimated the BPA "population-based half-life" (pop(1/2)) for a fasting time of 0-24 hr, < 4.5 hr, 4.5-8.5 hr, and > 8.5 hr.

Results: The overall pop(1/2) for the 0- to 24-hr interval was 43 hr [95% confidence interval (CI), 26-119 hr]. Among those reporting fasting times of 4.5-8.5 hr (n = 441), BPA declined significantly with fasting time, with a pop(1/2) of 4.1 hr (95% CI, 2.6-10.6 hr). However, within the fasting time intervals of 0-4.5 hr (n = 129) and 8.5-24 hr (n = 899), we saw no appreciable decline. Fasting time did not significantly predict highest (> 12 ng/mL) or lowest (below limit of detection) BPA levels.

Conclusions: Overall, BPA levels did not decline rapidly with fasting time in this sample. This suggests substantial nonfood exposure, accumulation in body tissues such as fat, or both. Explaining these findings may require experimental pharmacokinetic studies of chronic BPA exposure, further examination of BPA levels and effects in fat, and a search for important nonfood sources.

Keywords: NHANES; bisphenol A; exposure assessment; pharmacokinetics.

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Figures

Figure 1
Figure 1
Unadjusted urine BPA level versus fasting time. BPA is not creatinine-corrected; fasting time is self-reported. Points at 0.3 ng/mL BPA are < LOD (see “Methods”).
Figure 2
Figure 2
Adjusted urine BPA level versus fasting time. This plot shows BPA levels (± SE) by fasting time hour as determined by linear regression, adjusted for sex, age, race, poverty income ratio, BMI, session, and urine creatinine. Specific BPA levels are computed from the regression based on a “standard” person (see “Results“). SEs appear symmetrical because of the log scale. The size (area) of each point is proportional to the square root of the unweighted n (number of observations) in that fasting hour interval.

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