Association of urinary bisphenol A concentration with medical disorders and laboratory abnormalities in adults.

JAMA
Sep 2008
Citations:1239
Influential Citations:54
Observational Studies (Human)
83
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Methods
Cross-sectional NHANES 2003–2004 analysis of associations between urinary BPA concentrations and health status in the U.S. adult population. Participants: 1,455 adults aged 18–74 years with measured urinary BPA and urinary creatinine. Complex-sample design with weighting; regression models adjusted for age, sex, race/ethnicity, education, income, smoking, BMI, waist circumference, and urinary creatinine. Outcomes included eight blood-based analytes (CRP; GGT; alkaline phosphatase; lactate dehydrogenase; LDL-C; triglycerides; fasting glucose; fasting insulin) and major chronic diseases (cardiovascular disease, angina, coronary heart disease, heart attack, diabetes, liver disease, stroke, thyroid disease). Analyses used logistic regression for diagnoses and linear regression for biomarkers; 80% power to detect ORs of 1.4 per 1-SD change in BPA for prevalences around 5%.
Results
Higher urinary BPA concentrations were associated with higher odds of cardiovascular disease (OR per 1-SD increase in BPA, 1.39; 95% CI 1.18–1.63; P=0.001) and diabetes (OR per 1-SD increase, 1.39; 95% CI 1.21–1.60; P<0.001) after full adjustment. Higher BPA concentrations were also linked to clinically abnormal liver enzymes: GGT (OR per 1-SD increase, 1.29; 95% CI 1.14–1.46; P<0.001) and alkaline phosphatase (OR per 1-SD increase, 1.48; 95% CI 1.18–1.85; P=0.002). Associations persisted across alternative exposure metrics; in some analyses, highest BPA concentration quartile showed stronger associations with cardiovascular disease. No robust associations were found for several other conditions. Interpretation: higher BPA exposure, reflected by urinary BPA, may be linked to avoidable morbidity in community-dwelling adults; however, the cross-sectional design precludes causal inference, and replication with longitudinal data is needed.
Limitations
Cross-sectional design prevents causal inference; single-spot urinary BPA measurement may not reflect long-term exposure due to temporal variability. Potential residual confounding and measurement error; small numbers in some subgroups limit precision; results may not generalize beyond the U.S. adult population. Independent replication and longitudinal studies are needed to confirm causal relationships.

Abstract

CONTEXT Bisphenol A (BPA) is widely used in epoxy resins lining food and beverage containers. Evidence of effects in animals has generated concern over low-level chronic exposures in humans. OBJECTIVE To examine associations between urinary BPA con...