Urinary concentrations of phthalate metabolites during gestation and intrahepatic cholestasis of pregnancy: a population-based birth cohort study

被引:0
作者
Jian-Qing Wang
Hui Gao
Jie Sheng
Xing-Yong Tao
Kun Huang
Yun-Wei Zhang
Lei-Jing Mao
Shan-Shan Zhou
Zhong-Xiu Jin
Fang-Biao Tao
机构
[1] Anhui Medical University,Department of Maternal, Child and Adolescent Health, School of Public Health
[2] MOE Key Laboratory of Population Health Across Life Cycle,Anhui Provincial Key Laboratory of Population Health and Aristogenics
[3] NHC Key Laboratory of Study on Abnormal Gametes and Reproductive Tract,The Fourth Affiliated Hospital
[4] Anhui Medical University,undefined
[5] Anhui Medical University,undefined
来源
Environmental Science and Pollution Research | 2020年 / 27卷
关键词
Endocrine-disrupting chemicals; Phthalate; Monomethyl phthalate; Monobutyl phthalate; Intrahepatic cholestasis of pregnancy;
D O I
暂无
中图分类号
学科分类号
摘要
Phthalates, a class of widely used endocrine-disrupting chemicals (EDCs), are toxic to various organ systems in animals and humans. Intrahepatic cholestasis of pregnancy (ICP) is a reversible liver dysfunction causing cholestasis in late pregnancy. Evidence on the associations between exposure to phthalates and ICP is still lacking. In the present study, we investigated the relationships between urinary concentrations of phthalate metabolites and the risk of ICP in a Chinese population-based birth cohort. Pregnant women participated in the Ma’anshan Birth Cohort (MABC) study in China. Seven phthalate metabolites were detected in a urine sample in early pregnancy. Chemical concentrations were grouped by quartiles, and associations with outcomes were examined using logistic regression with adjustment for urine creatinine, race, education, poverty status, smoking status, alcohol consumption, maternal age, prepregnancy body mass index (BMI), parity, twin pregnancy, and pregnancy-related liver complications. Of 3474 women recruited into the Ma’anshan Birth Cohort, 2760 met the inclusion criteria and contributed to further analysis and biomonitoring data. Elevated odds ratios (ORs) of ICP were observed in the highest quartiles of monomethyl phthalate (MMP) exposure (OR = 1.59, 95% confidence intervals (CI) = 1.01–2.51) and monobutyl phthalate (MBP) exposure (OR = 1.82, 95% CI = 1.16–2.85) in the adjusted analyses. Our findings add to the evidence that supports the role of maternal phthalate exposure in the first trimester of gestation as a risk factor for ICP.
引用
收藏
页码:11714 / 11723
页数:9
相关论文
共 374 条
[1]  
Ai Y(2004)Clinical characteristics of 1241 cases of intrahepatic cholestasis of pregnancy Zhonghua Fu Chan Ke Za Zhi 39 217-220
[2]  
Liu SY(2011)Influence of lipid type on bis (2-ethylhexyl)phthalate (DEHP) leaching from infusion line sets in parenteral nutrition JPEN J Parenter Enteral Nutr 35 770-775
[3]  
Yao Q(2013)State of the science of endocrine disruptors Environ Health Perspect 121 A107-609
[4]  
Bagel S(2016)Phthalate pregnancy exposure and male offspring growth from the intra-uterine period to five years of age Environ Res 151 601-1485
[5]  
Dessaigne B(2014)Promoter DNA methylation of farnesoid X receptor and pregnane X receptor modulates the intrahepatic cholestasis of pregnancy phenotype PLoS One 9 e87697-443
[6]  
Bourdeaux D(2009)What additional factors beyond state-of-the-art analytical methods are needed for optimal generation and interpretation of biomonitoring data? Environ Health Perspect 117 1481-239
[7]  
Boyer A(2012)Ursodeoxycholic acid versus placebo, and early term delivery versus expectant management, in women with intrahepatic cholestasis of pregnancy: semifactorial randomised clinical trial BMJ 344 e3799-547
[8]  
Bouteloup C(1986)The importance of intrahepatic cholestasis of pregnancy Shanghai Med 9 440-292
[9]  
Bazin JE(2017)Phthalates and heavy metals as endocrine disruptors in food: a study on pre-packed coffee products Toxicol Rep 4 234-124
[10]  
Chopineau J(2012)The effects of di(2-ethylhexyl)phthalate exposure and selenium nutrition on sertoli cell vimentin structure and germ-cell apoptosis in rat testis Arch Environ Contam Toxicol 62 539-67