Atherosclerosis is a complex, multifactorial disease and the leading underlying cause of cardiovascular morbidity and mortality worldwide. Beyond traditional risk factors, grow-ing evidence highlights the critical role of environmental exposures in modulating ather-ogenesis. In real-world scenarios, individuals are exposed to complex mixtures of contam-inants, including particulate matter, toxic metals, pesticides, polycyclic aromatic hydro-carbons, and endocrine-disrupting chemicals. These combined exposures may exert addi-tive, synergistic or antagonistic effects, resulting in biological responses that cannot al-ways be predicted from single-agent exposures. At the cellular and molecular level, both chemical mixtures and environmental co-exposures converge on key pathogenic path-ways, including oxidative stress, endothelial dysfunction, chronic inflammation, and lipid dysregulation. These processes may favor monocyte recruitment, foam cell formation, vascular smooth muscle cell remodeling, and plaque instability. Moreover, cumulative exposures are associated with epigenetic alterations, such as dysregulation of DNA meth-ylation and non-coding expression patterns, which may influence long-term susceptibility to atherosclerosis. This structured narrative review synthesizes evidence from 37 studies investigating the cellular and molecular mechanisms underlying the impact of environ-mental mixtures and multipollutant co-exposures on atherosclerosis. By integrating evi-dence from epidemiological, toxicological, experimental, bioinformatics and multi-omics studies, while recognizing the predominantly associative nature of the available human evidence, we highlight emerging mechanistic insights and discuss the relevance of mix-ture-based approaches for improving risk assessment and informing future preventive strategies.

A Perfect Storm of Pollutants: Environmental Mixtures in the Pathogenesis of Atherosclerosis

Gorini Francesca
;
Palazzo Mariangela;Simonini Ludovica;Tonacci Alessandro;Rizza Antonio;Minichilli Fabrizio;Borghini Andrea
2026

Abstract

Atherosclerosis is a complex, multifactorial disease and the leading underlying cause of cardiovascular morbidity and mortality worldwide. Beyond traditional risk factors, grow-ing evidence highlights the critical role of environmental exposures in modulating ather-ogenesis. In real-world scenarios, individuals are exposed to complex mixtures of contam-inants, including particulate matter, toxic metals, pesticides, polycyclic aromatic hydro-carbons, and endocrine-disrupting chemicals. These combined exposures may exert addi-tive, synergistic or antagonistic effects, resulting in biological responses that cannot al-ways be predicted from single-agent exposures. At the cellular and molecular level, both chemical mixtures and environmental co-exposures converge on key pathogenic path-ways, including oxidative stress, endothelial dysfunction, chronic inflammation, and lipid dysregulation. These processes may favor monocyte recruitment, foam cell formation, vascular smooth muscle cell remodeling, and plaque instability. Moreover, cumulative exposures are associated with epigenetic alterations, such as dysregulation of DNA meth-ylation and non-coding expression patterns, which may influence long-term susceptibility to atherosclerosis. This structured narrative review synthesizes evidence from 37 studies investigating the cellular and molecular mechanisms underlying the impact of environ-mental mixtures and multipollutant co-exposures on atherosclerosis. By integrating evi-dence from epidemiological, toxicological, experimental, bioinformatics and multi-omics studies, while recognizing the predominantly associative nature of the available human evidence, we highlight emerging mechanistic insights and discuss the relevance of mix-ture-based approaches for improving risk assessment and informing future preventive strategies.
2026
Istituto di Fisiologia Clinica - IFC
atherosclerosis environmental mixtures, co-exposure multipollutant exposure, oxidative stress, inflammation, lipid dysregulation, endothelial dysfunction, epigenetics
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/595781
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