Kim Jin Hee, Hong Yun-Chul
Department of Integrative Bioscience & Biotechnology, Sejong University, 209 Neungdong-ro, Gwangjin-gu, Seoul, Republic of Korea.
Department of Preventive Medicine, Seoul National University College of Medicine, 28 Yongon-dong, Chongno-gu, Seoul, Republic of Korea.
Environ Health. 2017 Feb 15;16(1):8. doi: 10.1186/s12940-017-0221-9.
To verify oxidative stress as a possible mechanism that establishes a relationship between exposure to bisphenol A (BPA) and adverse health outcomes in the elderly Korean population, we evaluated the relation between visit-to-visit variations in urinary BPA and oxidative stress biomarker.
To assess the relation between BPA and urinary malondialdehyde (MDA) as an oxidative stress biomarker, we used a mixed effect model after controlling for age, sex, BMI, drinking status, exercise, urinary cotinine level, PM on lag day 2, and mean temperature and dew point on the day. The relation between exposure to BPA and MDA level by sex of participants and polymorphisms of oxidative stress-related genes (COX2, EPHX1, HSP70-hom, PON1, eNOS, CAT, DRD2, SOD2, and MPO) was also evaluated.
A significant association was found for BPA with MDA in both male and female elderly participants (male, β = 0.19 and p = 0.0003; female, β = 0.18 and p < .0001; and total, β = 0.18 and p < .0001). Furthermore, the association of BPA with MDA was found regardless of any genotype of the nine oxidative stress-related genes.
The results of our study suggest a strong association of BPA with oxidative stress, not related with sex and oxidative stress-related gene polymorphisms.
为验证氧化应激是否是建立韩国老年人群双酚A(BPA)暴露与不良健康结局之间关系的一种可能机制,我们评估了尿BPA访视间变化与氧化应激生物标志物之间的关系。
为评估BPA与作为氧化应激生物标志物的尿丙二醛(MDA)之间的关系,我们在控制了年龄、性别、体重指数、饮酒状况、运动、尿可替宁水平、滞后2天的颗粒物(PM)以及当天的平均温度和露点后,使用了混合效应模型。还评估了参与者性别和氧化应激相关基因(COX2、EPHX1、HSP70-hom、PON1、eNOS、CAT、DRD2、SOD2和MPO)多态性对BPA暴露与MDA水平之间关系的影响。
在老年男性和女性参与者中均发现BPA与MDA存在显著关联(男性,β = 0.19,p = 0.0003;女性,β = 0.18,p < 0.0001;总体,β = 0.18,p < 0.0001)。此外,无论九个氧化应激相关基因的任何基因型如何,均发现BPA与MDA存在关联。
我们的研究结果表明BPA与氧化应激之间存在强关联,且与性别和氧化应激相关基因多态性无关。