Ferguson Kelly K, McElrath Thomas F, Chen Yin-Hsiu, Mukherjee Bhramar, Meeker John D
Department of Environmental Health Sciences, University of Michigan School of Public Health, Ann Arbor, Michigan, USA.
Environ Health Perspect. 2015 Mar;123(3):210-6. doi: 10.1289/ehp.1307996. Epub 2014 Nov 14.
Phthalate exposure occurs readily in the environment and has been associated with an array of health end points, including adverse birth outcomes. Some of these may be mediated by oxidative stress, a proposed mechanism for phthalate action.
In the present study, we explored the associations between phthalate metabolites and biomarkers of oxidative stress measured in urine samples from multiple time points during pregnancy.
Women were participants in a nested case-control study of preterm birth (n = 130 cases, n = 352 controls). Each was recruited early in pregnancy and followed until delivery, providing urine samples at up to four visits. Nine phthalate metabolites were measured to assess exposure, and 8-hydroxydeoxyguanosine and 8-isoprostane were also measured in urine as markers of oxidative stress. Associations were assessed using linear mixed models to account for intraindividual correlation, with inverse selection probability weightings based on case status to allow for greater generalizability.
Interquartile range increases in phthalate metabolites were associated with significantly higher concentrations of both biomarkers. Estimated differences were greater in association with monobenzyl phthalate (MBzP), mono-n-butyl phthalate (MBP), and monoisobutyl phthalate (MiBP), compared with di(2-ethylhexyl) phthalate (DEHP) metabolites.
Urinary phthalate metabolites were associated with increased oxidative stress biomarkers in our study population of pregnant women. These relationships may be particularly relevant to the study of birth outcomes linked to phthalate exposure. Although replication is necessary in other populations, these results may also be of great importance for a range of other health outcomes associated with phthalates.
邻苯二甲酸盐在环境中易于接触,并且与一系列健康终点相关,包括不良出生结局。其中一些可能由氧化应激介导,这是邻苯二甲酸盐作用的一种假定机制。
在本研究中,我们探讨了邻苯二甲酸盐代谢物与孕期多个时间点尿液样本中测量的氧化应激生物标志物之间的关联。
女性参与了早产的巢式病例对照研究(130例病例,352例对照)。每位女性在孕期早期招募并随访至分娩,最多提供4次尿液样本。测量9种邻苯二甲酸盐代谢物以评估暴露情况,还测量尿液中的8-羟基脱氧鸟苷和8-异前列腺素作为氧化应激标志物。使用线性混合模型评估关联以考虑个体内相关性,并基于病例状态进行逆选择概率加权以提高普遍性。
邻苯二甲酸盐代谢物的四分位数间距增加与两种生物标志物的浓度显著升高相关。与邻苯二甲酸二(2-乙基己基)酯(DEHP)代谢物相比,估计与邻苯二甲酸单苄酯(MBzP)、邻苯二甲酸单正丁酯(MBP)和邻苯二甲酸单异丁酯(MiBP)的关联差异更大。
在我们的孕妇研究人群中,尿邻苯二甲酸盐代谢物与氧化应激生物标志物增加相关。这些关系可能与研究与邻苯二甲酸盐暴露相关的出生结局特别相关。虽然需要在其他人群中进行重复验证,但这些结果对于与邻苯二甲酸盐相关的一系列其他健康结局也可能非常重要。