Derivation of exposure factors for infant lactational exposure to persistent organic pollutants (POPs)

Sami Haddad1, Pierre Ayotte2, Marc-Andre Verner3

  • 1Department of Environmental and Occupational Health, School of Public Health, Université de Montréal, Montréal, QC, Canada; Université de Montréal Public Health Research Institute (IRSPUM), Université de Montréal, Montréal, QC, Canada; Chair in Toxicological Risk Assessment and Management, Université de Montréal, Montreal, QC, Canada.

Insights

Breastfeeding significantly impacts infant exposure to persistent organic pollutants (POPs). Infant doses can be much higher than maternal doses, especially for POPs with longer half-lives, informing early life risk assessments.

Area of Science:

  • Environmental Health
  • Toxicology
  • Pharmacokinetics

Background:

  • Infant exposure to persistent organic pollutants (POPs) via breastfeeding is a key concern for early life risk assessment.
  • Quantifying infant dose and biological levels relative to maternal levels is critical for understanding POP exposure dynamics.

Purpose of the Study:

  • To quantify infant exposure to POPs relative to their mothers during the first two years of life.
  • To derive infant:mother (I:M) ratios for both dose and biological levels of POPs.

Main Methods:

  • Utilized a validated pharmacokinetic model and Monte-Carlo simulations to model infant POP exposure.
  • Simulated POPs with varying half-lives (1-20 years) over the first two years of an infant's life.
  • Compared simulated I:M biological level ratios with measured ratios from Inuit mother-infant pairs for specific POPs (PCB-153, p,p'-DDE, HCB).

Main Results:

  • Peak I:M dose ratios were highest at lactation's onset, increasing with POP half-life.
  • Peak I:M biological level ratios occurred around one year postpartum, plateauing for POPs with half-lives >5 years.
  • Measured I:M biological level ratios in the Inuit cohort were generally below the simulated 95th percentile, validating the model.

Conclusions:

  • Simulated I:M dose and biological level ratios provide valuable tools for assessing risks associated with early life POP exposure through breastfeeding.
  • The model accurately reflects real-world infant exposure levels compared to maternal levels.
  • Findings highlight the importance of considering POP half-life in risk assessment for breastfed infants.

Related Concept Videos

Types of Toxins01:36

Types of Toxins

Humans continually engage with an environment rich in potentially harmful chemicals. These are introduced to our bodies through inhalation, ingestion, or skin contact. These chemicals exist in various forms, such as air and environmental pollutants, agricultural chemicals, organic solvents, and heavy metals.
Air pollutants, primarily gases, pose significant threats to respiratory health, leading to conditions like hypoxia, lung cancer, and in extreme cases, death.
Environmental pollutants like...
4.1K
Drug Dosing: Infants and Children01:29

Drug Dosing: Infants and Children

Pediatric patient dosages diverge from adults due to disparities in body surface area, total body water, and extracellular fluid per kilogram of body weight. The dosing regimen considers the variations in pharmacokinetics and pharmacology across distinct age groups, encompassing preterm newborns, infants, young children, older children, and adolescents. Calculation of pediatric patient doses is predicated on determining body surface area, which exhibits a superior correlation with the child's...
935
Toxicity Testing in Animals01:23

Toxicity Testing in Animals

Toxicity tests in animals are grounded on two main assumptions: first, the effects observed in laboratory animals can be extrapolated to humans, especially when adjusted for body surface area; second, high-dose exposure in animals is essential to identify potential human hazards from lower doses. This is based on the quantal dose-response concept, which faces the challenge of extrapolating results from relatively few test animals to much larger human populations. For example, a 0.01% incidence...
175
Probability Laws01:49

Probability Laws

Overview
45.4K
Relative Risk01:12

Relative Risk

Relative risk (RR) is a statistical measure commonly used in epidemiology to compare the likelihood of a particular event occurring between two groups. This metric is important for evaluating the relationship between exposure to a specific risk factor and the probability of a particular outcome. It plays a crucial role in medical research, public health studies, and risk assessment. Relative risk quantifies how much more (or less) likely an event is to occur in an exposed group compared to an...
2.6K
Pharmacokinetic–Pharmacodynamic Relationship: Exposure, Response and Effect01:26

Pharmacokinetic–Pharmacodynamic Relationship: Exposure, Response and Effect

The pharmacokinetic-pharmacodynamic (PK-PD) relationship describes the intricate link between drug exposure, efficacy, and toxicity, forming the foundation for optimal dosing regimens. This relationship uses mathematical modeling to characterize drug concentration-effect dynamics, ensuring precise therapeutic outcomes.Exposure represents the pharmacokinetic aspect of the PK-PD relationship, denoting the drug amount that elicits a biological response. It is typically quantified by administered...
244