Frederiksen Hanne, Kuiri-Hänninen Tanja, Main Katharina M, Dunkel Leo, Sankilampi Ulla
University Department of Growth and Reproduction, Rigshospitalet, Faculty of Health Sciences, Copenhagen, Denmark.
Environ Health Perspect. 2014 Sep;122(9):998-1005. doi: 10.1289/ehp.1307569. Epub 2014 May 30.
Some phthalates have shown antiandrogenic effects in rat offspring. Premature infants may be exposed to high amounts of specific phthalates during hospitalization, and thus are potentially at risk.
We evaluated longitudinal phthalate exposure and metabolism in full-term (FT) and preterm (PT) infants.
Fifty-eight FT and 67 PT (gestational age, 24.7-36.6 weeks) infants were recruited at birth and followed until 14 months (nine times). Urinary concentrations of metabolites of diethyl phthalate (DEP), dibutyl phthalate isomers (DiBP and DnBP), butylbenzyl phthalate (BBzP), di(2-ethylhexyl) phthalate (DEHP), and diisononyl phthalate (DiNP) were measured in 894 samples. Daily intake and a hazard index for antiandrogenic effects were estimated, and excretion patterns of DEHP and DiNP metabolites were analyzed.
Metabolites of BBzP, DiNP, and DEHP were 5-50 times higher at day 7 (D7) and month 1 (M1) in PT than in FT infants. Thereafter, metabolite concentrations were similar between the two groups. The estimated hazard index for combined DiBP, DnBP, BBzP, and DEHP exposures 7 days after birth exceeded the antiandrogenic threshold in > 80% of PT and > 30% of FT infants, and after M2, in 30% of all infants. The excretion pattern of DEHP and DiNP metabolites changed with age.
Most PT infants and approximately one-third of healthy FT newborns were exposed to phthalates during early life at a potentially harmful level according to the European Food Safety Authority's recommended limits of daily exposure. Changes in the relative proportions of secondary phthalate metabolites over time were consistent with maturation of infant metabolic pathways during the first year of life. Further research is needed on the health effects of phthalate exposures and the influence of changes in metabolic capacity in neonates and infants.
一些邻苯二甲酸盐已在大鼠后代中显示出抗雄激素作用。早产儿在住院期间可能会接触到大量特定邻苯二甲酸盐,因此存在潜在风险。
我们评估了足月儿(FT)和早产儿(PT)纵向邻苯二甲酸盐暴露及代谢情况。
招募了58名足月儿和67名早产儿(胎龄24.7 - 36.6周),自出生起进行随访直至14个月(共9次)。在894份样本中测量了邻苯二甲酸二乙酯(DEP)、邻苯二甲酸二丁酯异构体(DiBP和DnBP)、邻苯二甲酸丁苄酯(BBzP)、邻苯二甲酸二(2-乙基己基)酯(DEHP)和邻苯二甲酸二异壬酯(DiNP)的代谢物尿浓度。估算了每日摄入量及抗雄激素作用的危害指数,并分析了DEHP和DiNP代谢物的排泄模式。
在出生第7天(D7)和第1个月(M1)时,早产儿中BBzP、DiNP和DEHP的代谢物水平比足月儿高5 - 50倍。此后,两组间代谢物浓度相似。出生后7天,估计的DiBP、DnBP、BBzP和DEHP联合暴露危害指数超过抗雄激素阈值的早产儿超过80%,足月儿超过30%;在第2个月(M2)后,所有婴儿中有30%超过该阈值。DEHP和DiNP代谢物的排泄模式随年龄变化。
根据欧洲食品安全局推荐的每日暴露限值,大多数早产儿以及约三分之一健康的足月儿新生儿在生命早期接触邻苯二甲酸盐的水平可能有害。随着时间推移,次级邻苯二甲酸代谢物相对比例的变化与婴儿生命第一年代谢途径的成熟一致。需要进一步研究邻苯二甲酸盐暴露对健康的影响以及新生儿和婴儿代谢能力变化的影响。