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Emerging and Legacy Perfluoroalkyl Substances in Breastfed Chinese Infants: Renal Clearance, Body Burden, and
Jingzhi Yao1,2, Zhaomin Dong3, Lulin Jiang1
1State Environmental Protection Key Laboratory of Environmental Health Impact Assessment of Emerging Contaminants, School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai, China.
Insights
Emerging perfluoroalkyl substances (PFAS) are prevalent in Chinese human milk, posing potential health risks to infants due to high estimated daily intakes and long half-lives. Further research is needed to understand these risks.
Area of Science:
- Environmental Science
- Toxicology
- Public Health
Background:
- Human breast milk is a significant exposure pathway for perfluoroalkyl substances (PFAS) in infants.
- Understanding PFAS occurrence in human milk and infant toxicokinetics is crucial for assessing associated health risks.
Purpose of the Study:
- To determine levels of emerging and legacy PFAS in human milk and infant urine from China.
- To estimate renal clearance and predict infant serum PFAS levels.
- To evaluate potential health risks associated with infant exposure to PFAS.
Main Methods:
- Analysis of nine emerging and 13 legacy PFAS in 1,151 human milk samples and 80 paired infant cord blood and urine samples from China.
- Quantification using ultra-high-performance liquid chromatography tandem mass spectrometry.
- Estimation of renal clearance rates and prediction of infant serum PFAS concentrations using pharmacokinetic modeling.
Main Results:
- All nine emerging PFAS were detected in human milk, with 6:2 Cl-PFESA, PFMOAA, and PFO5DoDA exceeding 70% detection rates.
- Estimated daily intake (EDI) of PFOA and PFOS exceeded U.S. EPA reference doses in a significant proportion of infants.
- Emerging PFAS, particularly 6:2 Cl-PFESA, exhibited long estimated half-lives in infants, indicating prolonged exposure.
Conclusions:
- Emerging PFAS are widespread in human milk in China.
- High EDIs and extended half-lives of emerging PFAS suggest potential postnatal health risks for newborns.
- The study highlights the need for monitoring and risk assessment of emerging PFAS in vulnerable populations.
Background:
Human breast milk is a primary route of exposure to perfluoroalkyl substances (PFAS) in infants. To understand the associated risks, the occurrence of PFAS in human milk and the toxicokinetics of PFAS in infants need to be addressed.
Objectives:
We determined levels of emerging and legacy PFAS in human milk and urine samples from Chinese breastfed infants, estimated renal clearance, and predicted infant serum PFAS levels.
Methods:
In total, human milk samples were collected from 1,151 lactating mothers in 21 cities in China. In addition, 80 paired infant cord blood and urine samples were obtained from two cities. Nine emerging PFAS and 13 legacy PFAS were analyzed in the samples using ultra high-performance liquid chromatography tandem mass spectrometry. Renal clearance rates () of PFAS were estimated in the paired samples. PFAS serum concentrations in infants ( year of age) were predicted using a first-order pharmacokinetic model.
Results:
All nine emerging PFAS were detected in human milk, with the detection rates of 6:2 Cl-PFESA, PFMOAA, and PFO5DoDA all exceeding 70%. The level of 6:2 Cl-PFESA in human milk () ranked third after PFOA () and PFOS (). The estimated daily intake (EDI) values of PFOA and PFOS exceeded the reference dose (RfD) of recommended by the U.S. Environmental Protection Agency in 78% and 17% of breastfed infant samples, respectively. 6:2 Cl-PFESA had the lowest infant (), corresponding to the longest estimated half-life of 49 y. The average half-lives of PFMOAA, PFO2HxA, and PFO3OA were 0.221, 0.075, and 0.304 y, respectively. The of PFOA, PFNA, and PFDA were slower in infants than in adults.
Conclusions:
Our results demonstrate the widespread occurrence of emerging PFAS in human milk in China. The relatively high EDIs and half-lives of emerging PFAS suggest potential health risks of postnatal exposure in newborns. https://doi.org/10.1289/EHP11403.
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