Abstract 4369909: Association of right ventricular size and function parameters in Hodgkin and Non-Hodgkin Lymphoma with obesity and cardiovascular risk factors: What matters the most?

E Eduardo Villa Pallares (Mayo Clinic, Rochester, Rochester, Minnesota, United States) E Eduardo Brenner Muslera (Mayo Clinic, Rochester, Rochester, Minnesota, United States) M Maria Jose Perez Nuques (Mayo Clinic, Rochester, Rochester, Minnesota, United States) M MARIA F. GOMEZ ARDILA (Mayo Clinic, Rochester, Rochester, Minnesota, United States) E Eduardo Tellez Garcia (Mayo Clinic, Rochester, Rochester, Minnesota, United States) H Hector Villarraga (Mayo Clinic, Rochester, Rochester, Minnesota, United States)

Abstract

Introduction: Anthracycline-induced left ventricular dysfunction is well documented in lymphoma patients. However, the impact of cardiovascular risk factors (CVRF) and obesity on the right ventricle (RV) remains poorly characterized. Hypothesis: How does baseline CVRF burden—including obesity—affect RV structure and function over time in lymphoma patients treated with doxorubicin-based chemotherapy? Methods: A prospective cohort of patients with Hodgkin or non-Hodgkin lymphoma treated with doxorubicin-based chemotherapy at Mayo Clinic between March 1, 2013, and December 31, 2024, underwent echocardiography prior to chemotherapy initiation (T0), at 3–6 months (T1) and 6-18 months (T2) after treatment completion. A dedicated RV 4-Chamber view was used for all measurements. Patients were stratified into five groups: BMI>30, BMI>35, no CVRF, 1 CVRF (hypertension, diabetes, dyslipidemia, or smoking status), and ≥2 CVRF. RV parameters included end-diastolic/systolic area, FAC, TAPSE, S′ velocity, TRV, RVSP, and RV free wall strain. Group and time differences were analyzed using the Kruskal–Walli’s test due to non-normal distribution. Results: Among of 356 lymphoma patients (mean age 59.2 years, IQR:46-69) predominantly male (63.7%), 39.3% met criteria for obesity. At T0, patients with BMI >35 had greater RV end-diastolic (20.4 ± 4.4 vs. 18.7 ± 3.5 mm; p=0.009) and end-systolic diameters (11.0 ± 2.1 vs. 9.9 ± 2.6 mm; p=0.024), higher TRV (2.5 ± 0.4 vs. 2.2 ± 0.3 m/s; p<0.001) vs. no CVRFs. TAPSE was reduced vs. >2 CVRF group (23.7 ± 4.2 vs. 22.1 ± 4.8 mm; p=0.032). At T1, BMI >35 patients showed increased RV end-diastolic (22.3 ± 3.6 mm; p<0.001) and end-systolic areas (12.8 ± 2.9 mm; p<0.001), and worsened RVFWS (−24.0 ± 4.7% vs. −26.1 ± 2.98%; p=0.001) vs. no CVRF. RVSP was higher in those with >2 CVRFs (32.3 ± 5.4 mmHg; p=0.001). At T2, RVFWS was reduced in obese patients (−22.9 ± 3.5% vs. −27.1 ± 4.0%; p<0.001). RVSP stayed elevated in BMI >35 (33.0 mmHg) and >2 CVRFs (30.7 mmHg) vs. no CVRFs (23.7 mmHg; p<0.001). FAC and S′ did not differ significantly. Conclusion: In lymphoma patients treated with anthracyclines, isolated obesity was associated with the most pronounced RV changes—greater than those seen in non-obese patients with other CVRFs. These early and persistent alterations underscore the need for dedicated cardio-oncology care regardless of additional risk factors.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (6)

E

Eduardo Villa Pallares

Mayo Clinic, Rochester, Rochester, Minnesota, United States

E

Eduardo Brenner Muslera

Mayo Clinic, Rochester, Rochester, Minnesota, United States

M

Maria Jose Perez Nuques

Mayo Clinic, Rochester, Rochester, Minnesota, United States

M

MARIA F. GOMEZ ARDILA

Mayo Clinic, Rochester, Rochester, Minnesota, United States

E

Eduardo Tellez Garcia

Mayo Clinic, Rochester, Rochester, Minnesota, United States

H

Hector Villarraga

Mayo Clinic, Rochester, Rochester, Minnesota, United States