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Ambient Air Pollution and Congenital Heart Disease: Updated Evidence and Future Challenges
Francesca Gorini1, Alessandro Tonacci1
1Institute of Clinical Physiology, National Research Council, 56124 Pisa, Italy.
Insights
Maternal exposure to air pollution, particularly particulate matter (PM), is linked to congenital heart disease (CHD) risk. Further research is needed to confirm links with other pollutants and inform interventions.
Area of Science:
- Environmental Health
- Pediatric Cardiology
- Reproductive Toxicology
Background:
- Congenital heart disease (CHD) is a leading cause of infant mortality globally.
- Maternal exposure to environmental factors, including air pollution, is implicated in CHD development.
- Ambient air pollutants encompass particulate matter (PM), ozone, nitrogen dioxide, sulfur dioxide, and carbon monoxide.
Purpose of the Study:
- To review current evidence on the association between maternal exposure to outdoor air pollutants and CHD.
- To explore potential biological mechanisms underlying this association.
- To identify research gaps and future directions.
Main Methods:
- Literature review of human and experimental studies.
- Analysis of updated evidence on various air pollutants and CHD risk.
- Exploration of biological pathways.
Main Results:
- Moderate evidence links particulate matter (PM) exposure during pregnancy to increased overall CHD risk.
- Ozone exposure in the periconceptional period shows a potential association with increased CHD risk.
- Evidence for other pollutants (nitrogen dioxide, sulfur dioxide, carbon monoxide) is inconsistent.
Conclusions:
- Particulate matter and potentially ozone are associated with congenital heart disease risk.
- More research, including large cohort studies and animal models, is needed for other pollutants.
- Improved pollutant monitoring and AI analysis are crucial for understanding environmental impacts on CHD.
Abstract:
Congenital heart disease (CHD) represents the major cause of infant mortality related to congenital anomalies globally. The etiology of CHD is mostly multifactorial, with environmental determinants, including maternal exposure to ambient air pollutants, assumed to contribute to CHD development. While particulate matter (PM) is responsible for millions of premature deaths every year, overall ambient air pollutants (PM, nitrogen and sulfur dioxide, ozone, and carbon monoxide) are known to increase the risk of adverse pregnancy outcomes. In this literature review, we provide an overview regarding the updated evidence related to the association between maternal exposure to outdoor air pollutants and CHD occurrence, also exploring the underlying biological mechanisms from human and experimental studies. With the exception of PM, for which there is currently moderate evidence of its positive association with overall CHD risk following exposure during the periconception and throughout pregnancy, and for ozone which shows a signal of association with increased risk of pooled CHD and certain CHD subtypes in the periconceptional period, for the other pollutants, the data are inconsistent, and no conclusion can be drawn about their role in CHD onset. Future epidemiological cohort studies in countries with different degree of air pollution and experimental research on animal models are warranted to gain a comprehensive picture of the possible involvement of ambient air pollutants in CHD etiopathogenesis. While on the one hand this information could also be useful for timely intervention to reduce the risk of CHD, on the other hand, it is mandatory to scale up the use of technologies for pollutant monitoring, as well as the use of Artificial Intelligence for data analysis to identify the non-linear relationships that will eventually exist between environmental and clinical variables.
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