Pyrethroid Exposure in Premature Newborns: A Pilot Study on Materno-Fetal Transmission and Early Postnatal Evolution

Pauline Bressin1, Souleiman El Balkhi2,3, Chahrazed El Hamel1,4

  • 1Department of Pediatrics, University Hospital of Limoges, Limoges, France.

PubMed

Insights

Pyrethroid metabolites were found in nearly all mothers and 70% of premature newborns, indicating significant maternal-fetal transmission. This highlights the need for early monitoring of pesticide exposure in vulnerable infant populations.

Area of Science:

  • Environmental Health
  • Neonatal Toxicology
  • Perinatal Exposure Science

Background:

  • Pyrethroids are common insecticides with potential health implications.
  • Understanding fetal and neonatal exposure is crucial for public health.
  • Premature infants may represent a particularly vulnerable population to environmental toxins.

Purpose of the Study:

  • To investigate pyrethroid metabolite (MetaPyr) presence in mothers and premature newborns.
  • To assess transplacental transmission of MetaPyr.
  • To evaluate MetaPyr evolution in early neonatal life.

Main Methods:

  • Prospective study of 63 premature infants and 55 mothers (<34 weeks' gestation).
  • Urine samples collected for MetaPyr analysis.
  • Liquid chromatography-tandem mass spectrometry used for quantification.

Main Results:

  • MetaPyr detected in 98.2% of mothers and 70% of newborns within 3 days of birth.
  • Trans-DCCA and DBCA were the most common metabolites in newborns.
  • Newborn metabolites generally mirrored maternal presence, with some exceptions like FPBA.

Conclusions:

  • Evidence supports maternal-fetal pyrethroid metabolite transmission.
  • Metabolism and excretion of MetaPyr in neonates are complex.
  • Prenatal pyrethroid exposure is suggested, necessitating monitoring from birth in vulnerable groups.
Abstract

Related Concept Videos

Teratogenicity01:07

Teratogenicity

The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...
3.9K
Pharmacokinetics in Pediatric Patients: Drug Excretion01:26

Pharmacokinetics in Pediatric Patients: Drug Excretion

In pediatric medicine, understanding the renal function and drug elimination nuances is crucial for administering safe and effective treatments. Newborns, in particular, display markedly slower renal functions than adults, profoundly affecting how drugs are cleared from their bodies. This slower drug clearance requires clinicians to extend the dosing intervals for many medications to prevent drug accumulation and toxicity while ensuring therapeutic efficacy.One key area where these adjustments...
201
Pharmacokinetics in Pediatric Patients: Drug Metabolism01:24

Pharmacokinetics in Pediatric Patients: Drug Metabolism

In pediatric care, understanding the nuances of hepatic drug metabolism is crucial, as it significantly differs from that of adults. This divergence is primarily due to the developmental stage of drug-metabolizing enzymes, which affects how medications are processed in the body. In neonates, for instance, the activity of Phase I enzymes—critical for the initial breakdown of drugs—is markedly reduced, functioning at just 20–40% of the levels seen in adults. This reduction poses...
185