Abstract 4364886: The Association Between Tricuspid Regurgitation And Clinical Outcomes In Patients With Cardiac Amyloidosis

N Niyoosha Yoosefi (Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada, Vancouver, British Columbia, Canada) D Ding Yuan Wang (Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada, Vancouver, British Columbia, Canada) M Mehima Kang (Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada, Vancouver, British Columbia, Canada) B Bianca Zaidel (Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada, Vancouver, British Columbia, Canada) S Suzanne Ho (Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada, Vancouver, British Columbia, Canada) S Sean Virani (University of British Columbia, Vancouver, British Columbia, Canada) M Margot Davis (University of British Columbia, Vancouver, British Columbia, Canada)

Abstract

Background: Cardiac amyloidosis (CA) is a progressive infiltrative cardiomyopathy associated with poor prognosis. CA is commonly due to transthyretin (ATTR) or light chain (AL) amyloid deposition. Tricuspid regurgitation (TR) is a common echocardiographic finding in CA; however, its prognostic relevance remains unclear. We aimed to evaluate the association between TR severity and clinical outcomes in patients with CA. Methods: We conducted a retrospective cohort study of adults with CA referred to a specialized Cardiac Amyloidosis Clinic between January 2014-April 2024. TR severity was assessed by transthoracic echocardiography completed within 6 months of CA diagnosis and categorized as less-than-moderate versus moderate or greater. Multivariable Cox proportional hazards models were used to evaluate the association between TR severity and survival, adjusting for baseline characteristics including age, New York Heart Association (NYHA) class, estimated glomerular filtration rate (eGFR), natriuretic peptide levels (BNP or NT-proBNP), and disease stage. Results: Among 416 patients (mean age 64.8 years, 27% AL subtype), ≥moderateTR was present in 69 (16.6%). Compared to those <moderate TR, patients with ≥moderate TR were significantly older (76.8 vs 62.4 years, P = 0.016), had lower LVEF (46.7% vs 54.4%, P < 0.0001), higher pulmonary artery systolic pressure (PASP 45.3 mmHg vs 35.7 mmHg, P < 0.0001), and worse renal function (eGFR 55.4 vs 61.5 mL/min/m2, P = 0.027). ≥moderate TR was also associated with qualitatively more severe right ventricular dysfunction (P < 0.0001), RV dilation (incidence 49.3% vs 19.3%, P < 0.0001), and worse NYHA class (P = 0.0017). No significant associations were observed with sex, natriuretic peptide levels, troponin, amyloid subtype, or National Amyloidosis Centre stage (ATTR only). Patients with ≥moderate TR had significantly reduced survival following diagnosis (median 3.2 vs 5.4 years; log-rank P < 0.0001) (Figure 1). In adjusted Cox models, TR remained independently associated with mortality in the overall cohort (hazard ratio (HR) 1.84, P<0.0001), ATTR subgroup (HR 1.77, P = 0.0023), and AL subgroup (HR 2.18, P <0.0001). Conclusion: ≥moderateTR is independently associated with worse survival in patients with CA, regardless of amyloid subtype. These findings support routine TR severity assessment for risk stratification and to identify individuals who may benefit from closer follow-up or tailored interventions.

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 (7)

N

Niyoosha Yoosefi

Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada, Vancouver, British Columbia, Canada

D

Ding Yuan Wang

Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada, Vancouver, British Columbia, Canada

M

Mehima Kang

Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada, Vancouver, British Columbia, Canada

B

Bianca Zaidel

Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada, Vancouver, British Columbia, Canada

S

Suzanne Ho

Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada, Vancouver, British Columbia, Canada

S

Sean Virani

University of British Columbia, Vancouver, British Columbia, Canada

M

Margot Davis

University of British Columbia, Vancouver, British Columbia, Canada