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Published on: June 2, 2023
A longitudinal study of urinary phthalate excretion in 58 full-term and 67 preterm infants from birth through 14
Hanne Frederiksen1, Tanja Kuiri-Hänninen, Katharina M Main
1University Department of Growth and Reproduction, Rigshospitalet, Faculty of Health Sciences, Copenhagen, Denmark.
Insights
Preterm infants show higher phthalate exposure and antiandrogenic risk than full-term infants in early life. Phthalate metabolite levels normalize over time, suggesting developing metabolic pathways in infants.
Area of Science:
- Environmental Health
- Neonatal Toxicology
- Endocrine Disruption
Background:
- Phthalates are linked to antiandrogenic effects in animal studies.
- Premature infants face potential high phthalate exposure during hospitalization.
Purpose of the Study:
- To assess longitudinal phthalate exposure and metabolism in full-term and preterm infants.
- To evaluate antiandrogenic risk associated with phthalate exposure in neonates.
Main Methods:
- Recruited 58 full-term and 67 preterm infants, collecting 894 urine samples until 14 months.
- Measured urinary phthalate metabolites (DEP, DiBP, DnBP, BBzP, DEHP, DiNP).
- Estimated daily intake and hazard index for antiandrogenic effects.
Main Results:
- Preterm infants had 5-50x higher BBzP, DiNP, and DEHP metabolites at Day 7 and Month 1.
- Over 80% of preterm and 30% of full-term infants exceeded the antiandrogenic hazard threshold at 7 days postpartum.
- Metabolite excretion patterns changed with infant age, indicating evolving metabolic capacity.
Conclusions:
- Most preterm and many full-term infants experienced potentially harmful phthalate exposure levels early in life.
- Metabolic pathway maturation influences phthalate metabolite profiles during the first year.
- Further research is crucial for understanding health impacts and infant metabolic changes related to phthalates.
Background:
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.
Objective:
We evaluated longitudinal phthalate exposure and metabolism in full-term (FT) and preterm (PT) infants.
Methods:
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.
Results:
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.
Conclusion:
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.
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