» Articles » PMID: 33181246

Prevalence and Outcomes of Concomitant Aortic Stenosis and Cardiac Amyloidosis

Abstract

Background: Older patients with severe aortic stenosis (AS) are increasingly identified as having cardiac amyloidosis (CA). It is unknown whether concomitant AS-CA has worse outcomes or results in futility of transcatheter aortic valve replacement (TAVR).

Objectives: This study identified clinical characteristics and outcomes of AS-CA compared with lone AS.

Methods: Patients who were referred for TAVR at 3 international sites underwent blinded research core laboratory technetium-3,3-diphosphono-1,2-propanodicarboxylic acid (DPD) bone scintigraphy (Perugini grade 0: negative; grades 1 to 3: increasingly positive) before intervention. Transthyretin-CA (ATTR) was diagnosed by DPD and absence of a clonal immunoglobulin, and light-chain CA (AL) was diagnosed via tissue biopsy. National registries captured all-cause mortality.

Results: A total of 407 patients (age 83.4 ± 6.5 years; 49.8% men) were recruited. DPD was positive in 48 patients (11.8%; grade 1: 3.9% [n = 16]; grade 2/3: 7.9% [n = 32]). AL was diagnosed in 1 patient with grade 1. Patients with grade 2/3 had worse functional capacity, biomarkers (N-terminal pro-brain natriuretic peptide and/or high-sensitivity troponin T), and biventricular remodeling. A clinical score (RAISE) that used left ventricular remodeling (hypertrophy/diastolic dysfunction), age, injury (high-sensitivity troponin T), systemic involvement, and electrical abnormalities (right bundle branch block/low voltages) was developed to predict the presence of AS-CA (area under the curve: 0.86; 95% confidence interval: 0.78 to 0.94; p < 0.001). Decisions by the heart team (DPD-blinded) resulted in TAVR (333 [81.6%]), surgical AVR (10 [2.5%]), or medical management (65 [15.9%]). After a median of 1.7 years, 23% of patients died. One-year mortality was worse in all patients with AS-CA (grade: 1 to 3) than those with lone AS (24.5% vs. 13.9%; p = 0.05). TAVR improved survival versus medical management; AS-CA survival post-TAVR did not differ from lone AS (p = 0.36).

Conclusions: Concomitant pathology of AS-CA is common in older patients with AS and can be predicted clinically. AS-CA has worse clinical presentation and a trend toward worse prognosis, unless treated. Therefore, TAVR should not be withheld in AS-CA.

Citing Articles

Echocardiography and Heart Failure: An Echocardiographic Decision Aid for the Diagnosis and Management of Cardiomyopathies.

Pender A, Lewis-Owona J, Ekiyoyo A, Stoddard M Curr Cardiol Rep. 2025; 27(1):64.

PMID: 40019673 PMC: 11870920. DOI: 10.1007/s11886-025-02194-y.


Advances and challenges in echocardiographic diagnosis and management of cardiac amyloidosis.

Tian Y, Liu H Int J Cardiovasc Imaging. 2025; .

PMID: 40009119 DOI: 10.1007/s10554-025-03362-5.


Future challenges of imaging in cardiac amyloidosis.

Hauptmann L, Autherith M, Kammerlander A, Duca F, Nitsche C Int J Cardiovasc Imaging. 2025; .

PMID: 39971842 DOI: 10.1007/s10554-025-03353-6.


Prognostic value of computed tomography-derived myocardial extracellular volume in aortic stenosis: a meta-analysis of all-cause mortality and heart failure hospitalization.

Kirigaya J, Kato S, Matsushita K, Horita N, Utsunomiya D, Hibi K Eur Heart J Open. 2025; 5(1):oeaf007.

PMID: 39912102 PMC: 11795651. DOI: 10.1093/ehjopen/oeaf007.


Biomarkers to Predict Abnormal Technetium-99m Pyrophosphate Scans in Patients With Suspected Transthyretin Amyloidosis.

De Michieli L, AbouEzzeddine O, Abbasi M, Davies D, Scott C, Muchtar E JACC CardioOncol. 2025; 7(1):70-78.

PMID: 39896120 PMC: 11781999. DOI: 10.1016/j.jaccao.2024.10.013.


References
1.
Gillmore J, Maurer M, Falk R, Merlini G, Damy T, Dispenzieri A . Nonbiopsy Diagnosis of Cardiac Transthyretin Amyloidosis. Circulation. 2016; 133(24):2404-12. DOI: 10.1161/CIRCULATIONAHA.116.021612. View

2.
Castano A, Narotsky D, Hamid N, Khalique O, Morgenstern R, DeLuca A . Unveiling transthyretin cardiac amyloidosis and its predictors among elderly patients with severe aortic stenosis undergoing transcatheter aortic valve replacement. Eur Heart J. 2017; 38(38):2879-2887. PMC: 5837725. DOI: 10.1093/eurheartj/ehx350. View

3.
Maurer M, Bokhari S, Damy T, Dorbala S, Drachman B, Fontana M . Expert Consensus Recommendations for the Suspicion and Diagnosis of Transthyretin Cardiac Amyloidosis. Circ Heart Fail. 2019; 12(9):e006075. PMC: 6736650. DOI: 10.1161/CIRCHEARTFAILURE.119.006075. View

4.
Coffey S, Cox B, Williams M . The prevalence, incidence, progression, and risks of aortic valve sclerosis: a systematic review and meta-analysis. J Am Coll Cardiol. 2014; 63(25 Pt A):2852-61. DOI: 10.1016/j.jacc.2014.04.018. View

5.
Scully P, Patel K, Treibel T, Thornton G, Hughes R, Chadalavada S . Prevalence and outcome of dual aortic stenosis and cardiac amyloid pathology in patients referred for transcatheter aortic valve implantation. Eur Heart J. 2020; 41(29):2759-2767. PMC: 7395329. DOI: 10.1093/eurheartj/ehaa170. View