Key result
Higher hepatic ECV linked to ~62% increased mortality risk.
Why the study?
Conventional imaging parameters incompletely capture the systemic consequences of tricuspid regurgitation, prompting investigation into whether CMR-derived hepatic extracellular volume fraction provides prognostic information.
Does higher hepatic extracellular volume fraction (ECV) measured by CMR predict all-cause mortality in patients with moderate or greater tricuspid regurgitation?
Does higher hepatic extracellular volume fraction (ECV) measured by CMR predict all-cause mortality in patients with moderate or greater tricuspid regurgitation?
Hepatic extracellular volume fraction measured by CMR provides independent and incremental prognostic value for all-cause mortality in patients with moderate or greater tricuspid regurgitation.
Answers are grounded in this paper and cite their sources.
Hypothesis-generating for hepatic ECV in TR risk stratification; prospective validation needed before clinical adoption.
BACKGROUND: Tricuspid regurgitation (TR) leads to systemic venous congestion and congestive hepatopathy, but conventional TR imaging parameters incompletely capture systemic consequences. Hepatic extracellular volume fraction (ECV) on cardiac magnetic resonance T1 mapping may reflect hepatic tissue remodeling and provide prognostic information beyond conventional risk markers. METHODS: Consecutive patients with moderate or greater TR who underwent cardiac magnetic resonance with hepatic T1 mapping were studied. Hepatic ECV was calculated using pre- and postcontrast T1 values and hematocrit. Patients were stratified by hepatic ECV tertiles. The primary end point was all-cause mortality. RESULTS: Among 234 patients (mean age, 65.6±15.8 years; 46.2% men), mean hepatic ECV was 37.7±9.0%, with tertile cutoffs at 32.5% and 41.3%. Higher hepatic ECV tertiles were associated with worse biventricular function and greater TR severity. Right ventricular ejection fraction decreased across tertiles (48.2% versus 48.5% versus 40.3%, P <0.001), while right ventricular end-diastolic volume index increased (107.4 versus 105.4 versus 127.4 mL/m², P <0.001). The prevalence of severe TR (regurgitant fraction ≥50%) increased from 10.9% (mean) across tertiles 1 and 2 to 29.5% in tertile 3 ( P <0.001). During a mean follow-up of 2.2 years, 43 (18.4%) deaths occurred. Mortality increased across hepatic ECV tertiles: 12.8% versus 11.5% versus 30.8% ( P =0.002 for trend). Kaplan-Meier analysis showed 3-year survival rates of 88%, 89%, and 57% across tertiles 1, 2, and 3, respectively. In multivariable Cox regression adjusting for age, right ventricular dysfunction, and severe TR, hepatic ECV tertiles remained independently predictive of mortality (HR, 1.62 [95% CI, 1.06–2.48]; P =0.027). Forward stepwise analysis yielded significant incremental prognostic value beyond traditional TR risk factors, improving model discrimination from χ²=24.4 to 30.1 ( P =0.02). CONCLUSIONS: Hepatic ECV is a novel prognostic marker that provides incremental risk stratification in TR and has potential to impact therapeutic decision-making in the era of expanded treatment options for TR.
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Calle et al. (2026) studied this question. Higher hepatic extracellular volume fraction tertiles were associated with increased mortality, with a 3-year survival rate of 57% in tertile 3 compared to 88% in tertile 1 (HR 1.62).
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