Abstract 4148121: Identification of Acute Air Pollution Induced Altered Metabolomic Pathways that May Lead to CAD and AMI: the BioHEART-CT Study

Background: Outdoor air pollution, a persistent threat since the Industrial Revolution, continues to pose a global challenge with severe implications for public health. Despite advancements, air quality issues —particularly particulate matter —are associated with diseases like coronary artery disease (CAD) and stroke. The unknown pathophysiology that links air pollution to cardiovascular diseases is a pressing issue that demands immediate attention. Understanding these mechanisms is critical for effective prevention and treatment. Methods: The BioHEART-CT Discovery cohort included 1,002 adults referred for elective CTCA (2015-2020). Blood (20-30 ml) was collected at the time of CTCA, processed, stored at -80°C, and analysed using Agilent 1260 LC and QTRAP 5500 MS. Maximum daily PM2.5 was measured using home postcodes and publicly available land-based monitors. After normalisation, PCA and PLS-DA were employed to reduce dimensionality and identify significant variables, followed by pathway analysis of significant metabolites using metabolite set enrichment analysis. Results: Using the threshold of PM 2.5 ≥12 μg/m 3 to categorise patients into high vs low-exposure, low-exposure subjects formed a distinct cluster from high-exposure subjects. PLS-DA clustering with ten-fold cross-validation identified key metabolites with high VIP scores: transHYP, betaine, and alanine. Metabolite set enrichment analysis revealed significant pathways: Glycine, Serine, and Threonine metabolism, and Arginine and Proline metabolism (p<0.001, FDR <0.05) (Figure 1). Conclusion: Our study's most significant finding—the enriched metabolic set of glycine, serine, and threonine metabolism, along with arginine and proline metabolism—has been implicated in the development of CAD in previous studies. These findings can potentially inform preventive and treatment strategies, making a real difference in the lives of those affected by air pollution-related cardiovascular diseases.

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Journal
Circulation
Published
2024-11-12
DOI
https://doi.org/10.1161/circ.150.suppl_1.4148121
Primary Topic
Air Quality Monitoring and Forecasting
Type
article
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article

Abstract 4148121: Identification of Acute Air Pollution Induced Altered Metabolomic Pathways that May Lead to CAD and AMI: the BioHEART-CT Study

Gemma Alexandra Figtree, Michael P. Gray, S. Fathieh, Owen Tang et al.
Circulation
Air Quality Monitoring and Forecasting
article

Abstract 4148121: Identification of Acute Air Pollution Induced Altered Metabolomic Pathways that May Lead to CAD and AMI: the BioHEART-CT Study

Gemma Alexandra Figtree, Michael P. Gray, S. Fathieh, Owen Tang, Thomas Astell‐Burt, Stuart M. Grieve
article en

Abstract

Background: Outdoor air pollution, a persistent threat since the Industrial Revolution, continues to pose a global challenge with severe implications for public health. Despite advancements, air quality issues —particularly particulate matter —are associated with diseases like coronary artery disease (CAD) and stroke. The unknown pathophysiology that links air pollution to cardiovascular diseases is a pressing issue that demands immediate attention. Understanding these mechanisms is critical for effective prevention and treatment. Methods: The BioHEART-CT Discovery cohort included 1,002 adults referred for elective CTCA (2015-2020). Blood (20-30 ml) was collected at the time of CTCA, processed, stored at -80°C, and analysed using Agilent 1260 LC and QTRAP 5500 MS. Maximum daily PM2.5 was measured using home postcodes and publicly available land-based monitors. After normalisation, PCA and PLS-DA were employed to reduce dimensionality and identify significant variables, followed by pathway analysis of significant metabolites using metabolite set enrichment analysis. Results: Using the threshold of PM 2.5 ≥12 μg/m 3 to categorise patients into high vs low-exposure, low-exposure subjects formed a distinct cluster from high-exposure subjects. PLS-DA clustering with ten-fold cross-validation identified key metabolites with high VIP scores: transHYP, betaine, and alanine. Metabolite set enrichment analysis revealed significant pathways: Glycine, Serine, and Threonine metabolism, and Arginine and Proline metabolism (p<0.001, FDR <0.05) (Figure 1). Conclusion: Our study's most significant finding—the enriched metabolic set of glycine, serine, and threonine metabolism, along with arginine and proline metabolism—has been implicated in the development of CAD in previous studies. These findings can potentially inform preventive and treatment strategies, making a real difference in the lives of those affected by air pollution-related cardiovascular diseases.

CirculationVol. 150(Suppl_1)
The University of Sydney (AU), Royal Prince Alfred Hospital (AU), UNSW Sydney (AU)
Good health and well-being
Openalex Percentile: Top 82%
Air Quality Monitoring and Forecasting
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