# Air Pollution and Cardiac Remodeling and Function in Patients With Breast Cancer

**Authors:** Wonyoung Jung, Kyunga Ko, Amanda M. Smith, Anran Huang, Congying Xia, Yehoda M. Martei, Vivek K. Narayan, Amy S. Clark, Benedicte Lefebvre, Kellie McDermott, Daniel Koropeckyj-Cox, Omotayo Fasan, Alexander Hutsell, Amber Daniels, Virginia Englefield, Kasey J. Leger, Kelly D. Getz, Hari K. Narayan, Julian D. Marshall, Tiffany M. Powell-Wiley, Clyde W. Yancy, Bonnie Ky

PMC · DOI: 10.1001/jamanetworkopen.2025.52323 · JAMA Network Open · 2026-01-15

## TL;DR

Breast cancer patients exposed to higher levels of fine particulate matter and ozone had worse heart function and more cardiac remodeling.

## Contribution

This study is the first to show a link between air pollution exposure and cardiac dysfunction in breast cancer patients undergoing cardiotoxic therapies.

## Key findings

- Higher PM2.5 and ozone exposure were associated with reduced left ventricular ejection fraction and worse cardiac function.
- Patients in the highest tertiles of PM2.5 and ozone exposure had significantly increased risk of cardiac dysfunction.
- PM10 and nitrogen dioxide showed no significant associations with cardiac dysfunction.

## Abstract

This cohort study assesses associations between exposure to air pollutants and changes in cardiac structure, function, and remodeling in patients with breast cancer treated with potentially cardiotoxic therapies.

Is exposure to air pollutants associated with cardiac remodeling and function among women with breast cancer treated with potentially cardiotoxic therapies?

In a cohort study of 580 patients with breast cancer treated with anthracyclines and/or trastuzumab, greater exposure to fine particulate matter with diameter of 2.5 µm or less and ozone was associated with worse cardiac remodeling and function and greater risk of therapy-related cardiac dysfunction. Exposure to particulate matter with diameter of 10 µm or less and nitrogen dioxide showed limited associations.

This study’s comprehensive structural and functional data support the critical need for strategies to reduce fine particulate matter and ozone exposure, particularly in patients with breast cancer.

The relationship between air pollution and cardiac remodeling in patients with cancer treated with cardiotoxic therapy is undefined.

To assess the associations between air pollutants and changes in cardiac function, structure, and remodeling in patients with breast cancer treated with anthracyclines and/or trastuzumab therapy.

This longitudinal prospective cohort study included patients with breast cancer enrolled at multiple sites of a quaternary health care system from July 1, 2010, to November 1, 2018. All participants were initiating anthracyclines and/or trastuzumab. Data were analyzed from December 1, 2024, to April 30, 2025.

Three-year average census tract–level concentrations of fine particulate matter with diameter of 2.5 µm or less (PM2.5), particulate matter with diameter of 10 µm or less (PM10), nitrogen dioxide (NO2), and ozone (O3).

Core laboratory–quantified, echocardiography-derived measures of cardiac remodeling and function and incidence of cardiac dysfunction, defined as a left ventricular ejection fraction (LVEF) decline of 10% or more from baseline to less than 50%. Multivariable linear regression and generalized estimating equations defined the cross-sectional and longitudinal associations between air pollution and measures of cardiac remodeling and function. Cause-specific hazard models defined the adjusted associations between air pollution and cardiac dysfunction.

Across 580 female patients (median age, 50 years [IQR, 42-58 years]), 3642 echocardiograms were obtained at standardized time intervals over a median of 3.1 years (IQR, 2.3-3.6 years) and centrally quantified. Cardiac dysfunction was observed in 98 of 574 participants (17.1%). Concentrations of PM2.5 (median, 9.26 μg/m3 [IQR, 8.49-10.17 μg/m3]) and O3 (median, 47.00 parts per billion [ppb] [IQR, 45.50-48.19 ppb]) were each associated with cardiac dysfunction and adverse remodeling, cross-sectionally and longitudinally. Over time, each IQR-increment increase in PM2.5 (1.68 μg/m3) and O3 (2.69 ppb) was associated with a mean LVEF change of −1.3% (95% CI, −1.8% to −0.8%) and −1.4% (95% CI, −1.8% to −1.0%), respectively; worse longitudinal strain (−1.0% [95% CI, −1.3% to −0.7%] and −1.1% [95% CI, −1.3% to −0.8%], respectively); and left ventricular mass increase of 4.8 g/m2 (95% CI, 3.1-6.5 g/m2) and 3.2 g/m2 (95% CI, 2.1-4.3 g/m2), respectively. Patients in the highest tertiles of PM2.5 (adjusted hazard ratio [AHR], 2.03; 95% CI, 1.17-3.52) and O3 (AHR, 2.15; 95% CI, 1.23-3.78) exposure were at a significantly higher risk of cardiac dysfunction compared with those in the lowest tertile. Neither PM10 (AHR, 0.84; 95% CI, 0.49-1.44) nor NO2 (AHR, 0.92; 95% CI, 0.50-1.70) showed significant associations with cardiac dysfunction.

In this cohort study, PM2.5 and O3 exposure was independently associated with worse cardiac remodeling and function in patients with breast cancer treated with cardiotoxic therapy. These findings highlight the importance of modifying environmental exposures to mitigate cardiovascular disease risk.

## Linked entities

- **Chemicals:** nitrogen dioxide (PubChem CID 3032552), ozone (PubChem CID 24823)
- **Diseases:** breast cancer (MONDO:0004989)

## Full-text entities

- **Diseases:** cancer (MESH:D009369), Cardiac Remodeling (MESH:D020257), Breast Cancer (MESH:D001943), Cardiac dysfunction (MESH:D006331), cardiotoxic (MESH:D066126), left ventricular mass (MESH:D018487), cardiovascular disease (MESH:D002318)
- **Chemicals:** anthracyclines (MESH:D018943), PM10 (-), NO2 (MESH:D009585), trastuzumab (MESH:D000068878), O3 (MESH:D010126)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12809362/full.md

## References

54 references — full list in the complete paper: https://tomesphere.com/paper/PMC12809362/full.md

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Source: https://tomesphere.com/paper/PMC12809362