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Increase of urinary malondialdehyde level by bisphenol A exposure: a longitudinal panel study
Jin Hee Kim1, Yun-Chul Hong2,3
1Department of Integrative Bioscience & Biotechnology, Sejong University, 209 Neungdong-ro, Gwangjin-gu, Seoul, Republic of Korea. jhkim777@sejong.ac.kr.
This study found a strong link between Bisphenol A (BPA) exposure and oxidative stress in the elderly Korean population. The association between BPA and malondialdehyde (MDA), an oxidative stress biomarker, was consistent across sexes and genetic variations.
Area of Science:
- Environmental Health
- Toxicology
- Gerontology
Background:
- Investigated the potential role of oxidative stress in linking Bisphenol A (BPA) exposure to adverse health outcomes in elderly Koreans.
- Examined the relationship between short-term variations in urinary BPA levels and an oxidative stress biomarker.
Purpose of the Study:
- To verify oxidative stress as a mechanism connecting BPA exposure to health issues in the elderly.
- To assess the association between BPA and urinary malondialdehyde (MDA), a marker of oxidative stress.
Main Methods:
- Utilized a mixed-effects model to analyze the relationship between urinary BPA and MDA.
- Controlled for various covariates including age, sex, BMI, lifestyle factors, and environmental exposures (PM10, temperature, dew point).
- Evaluated the influence of sex and polymorphisms in nine oxidative stress-related genes on the BPA-MDA association.
Main Results:
- A significant positive association was observed between BPA and MDA levels in both male and female elderly participants.
- The association between BPA and MDA remained significant across all participants, irrespective of sex.
- The relationship between BPA and MDA was not influenced by the genotypes of the nine studied oxidative stress-related genes.
Conclusions:
- Concluded a strong association between Bisphenol A (BPA) exposure and oxidative stress in the elderly Korean population.
- The observed association was independent of participant sex and variations in specific oxidative stress-related gene polymorphisms.
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