Key result
Higher visceral adiposity linked to ~2.1-point greater LVEF decline per SD during cardiotoxic breast cancer therapy.
Why the study?
Cardiovascular disease is an important cause of death in early breast cancer survivors, and body composition abnormalities linked to adverse cardiovascular outcomes are not well captured by BMI and remain understudied.
Does baseline body composition predict longitudinal changes in cardiac function in women with early breast cancer receiving cardiotoxic chemotherapy?
Cohort (n=182)
No
Does baseline body composition predict longitudinal changes in cardiac function in women with early breast cancer receiving cardiotoxic chemotherapy?
Effect estimate: -2.1 LVEF points per 1-SD increase (95% CI -4.1 to -0.1)
p-value: p=0.04
Baseline visceral adiposity is associated with worsening longitudinal changes in systolic and diastolic function in women undergoing cardiotoxic breast cancer therapy.
May inform risk stratification during cardiotoxic therapy; hypothesis-generating and requires prospective validation before clinical adoption.
12021 Background: Anthracyclines and HER2-directed therapies have improved survival in early breast cancer (EBC), but cardiotoxicity remains a concern for long-term survivors. Cardiovascular disease may ultimately exceed breast cancer as a cause of death, highlighting the need for better understanding of therapy-related cardiac dysfunction. Body composition abnormalities are linked to adverse cardiovascular outcomes but are not well captured by body mass index are understudied. We evaluated longitudinal associations between baseline CT-derived body composition and echocardiography measures of cardiac structure and function. Methods: This is a retrospective analysis of women with stage I–III EBC treated with anthracyclines and/or trastuzumab at the University of Pennsylvania. Eligible patients had a pre-treatment and ≥1 follow-up echocardiogram and pre-treatment abdominal CT or PET-CT imaging for body composition assessment. L3-based segmentation quantified skeletal muscle mass, muscle density (SMD), subcutaneous and visceral adiposity (SAT, VAT), and adipose tissue density (SATD, VATD). Core-lab echocardiographic outcomes included systolic function (LVEF, GLS) and diastolic function (E/e′). Using multivariable-adjusted generalized estimating equations (GEE) models, we evaluated longitudinal associations between baseline body composition (per 1-SD increase) and two complementary outcomes for each metric: (1) absolute values over time (overall burden) and (2) change from baseline (within-participant worsening). Results: Across 182 participants, the median age was 49.5 years (Q1-Q3 41–60), HER2-positive disease was present in 64 (35.4%), estrogen receptor–positive disease in 114 (62.6%), and triple-negative disease in 37 (20.4%). Anthracycline-based therapy was administered to 150 (82.4%), radiation therapy to 140 (76.9%), and mastectomy was performed in 106 (58.6%). Baseline hypertension, hyperlipidemia, and diabetes were present in 56 (30.8%), 43 (23.6%), and 12 (6.6%), respectively. In multivariable-adjusted GEE models, higher baseline VAT was associated with a greater decline in LVEF over time (−2.1 LVEF points per 1-SD increase; 95% CI −4.1 to −0.1; p=0.04). We next evaluated diastolic function, where higher baseline VAT was associated with a greater increase in E/e′ over time (β 0.38 per 1-SD increase; 95% CI, 0.01 to 0.74; p=0.04). In models evaluating absolute E/e′ over time, higher VAT (β 0.51; 95% CI, 0.11 to 0.91) and SAT (β 0.37; 95% CI, 0.06 to 0.59), and lower SMD (β −0.34; 95% CI, −0.66 to −0.02) and VAT density (β −0.36; 95% CI, −0.67 to −0.05) were associated with higher E/e′. No adjusted associations were observed for longitudinal change in GLS (all p>0.05). Conclusions: Baseline visceral adiposity was associated with worsening in longitudinal changes in systolic and diastolic function during cardiotoxic breast cancer therapy.
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Aleixo et al. (2026) conducted a cohort in Early breast cancer (n=182). Baseline visceral adiposity (VAT) was evaluated on Decline in LVEF over time (-2.1 LVEF points per 1-SD increase, 95% CI -4.1 to -0.1, p=0.04). Higher baseline visceral adiposity was associated with a greater decline in LVEF (-2.1 points per 1-SD increase; 95% CI -4.1 to -0.1; p=0.04) during cardiotoxic breast cancer therapy.
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