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Updated: May 12, 2026

Long-term Behavioral and Reproductive Consequences of Embryonic Exposure to Low-dose Toxicants
Published on: March 6, 2018
Examining risk assessment implications of genetic and dose-dependent dynamics of lead exposure in breastfeeding using
Danila Cuomo1, Zhuolin Song2,3,4, Megan Nitcher1
1Department of Cell Biology and Genetics, Texas A&M University, College Station, TX 77843, United States.
Insights
Genetic background significantly impacts lead exposure in breastfed infants. This study highlights the need to consider population variability in risk assessments for infant lead exposure via breastfeeding.
Area of Science:
- Environmental Health
- Toxicology
- Genetics
Background:
- Breastfeeding provides benefits but can transmit lead (Pb) to infants.
- Infants are highly susceptible to lead's adverse effects.
- Limited data exist on lead exposure risks for breastfed infants.
Purpose of the Study:
- To investigate how breastfeeding influences offspring blood lead levels (BLL).
- To quantify population variation in BLL among different mouse strains and doses.
- To inform public health strategies for mitigating lead exposure risks in infants.
Main Methods:
- Assessed BLL in mouse dams and offspring across 14 Collaborative Cross (CC) strains.
- Administered low (100 ppm) and high (1,000 ppm) lead doses to dams during lactation.
- Analyzed genetic background as a factor in lead accumulation and transfer.
Main Results:
- Significant interstrain variability in BLL was observed in dams and offspring.
- Genetic background was a primary driver of BLL variation.
- Observed BLL variability in dams surpassed regulatory estimates, emphasizing population differences.
Conclusions:
- Genetic factors play a crucial role in lead exposure via breastfeeding.
- Current regulatory risk assessments may underestimate population variability.
- Integrating genetic variability is essential for accurate risk assessment and public health guidance.
Abstract:
Breastfeeding offers well-documented advantages but may inadvertently introduce lead (Pb) exposure to infants. Scarce data exist on the risks of Pb exposure for breastfed infants, and strategies for risk mitigation are needed, particularly considering the heightened susceptibility of children to adverse effects from Pb exposure. To investigate the potential influence of breastfeeding on blood Pb levels (BLL) in offspring, population variation in BLL between nonparous and parous mouse dams was quantified, as well as in dams exposed to low and high dose while breastfeeding, and their offspring. Female mice from 14 distinct collaborative cross (CC) mouse strains were mated with sires from different CC strains to produce 14 F1 hybrids. Subsequently, dams were administered either low- (100 ppm) or high- (1,000 ppm) dose Pb through ad libitum access drinking water starting the day of delivery for a duration of 4 wk, leading to the subsequent exposure of the offspring via lactation. Genetic background emerged as a predominant factor contributing to variation, with substantial interstrain variability observed in both CC dams and F1 hybrids exposed to low and high doses of Pb. Crucially, the degree of variation in BLL among CC dams exceeded the default variability estimate (geometric SD = 1.6) utilized in regulatory standard settings. These findings underscore the importance of integrating population variability in risk assessment. Ultimately, this study provides critical insights to guide public health decision-making processes concerning Pb exposure through breastfeeding and its potential implications for infants' health.
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