Background and aims: The aims of this study were to assess prescription patterns, dosages, discontinuation rates and association with prognosis of conventional heart failure (HF) medications in patients with transthyretin cardiac amyloidosis (ATTR-CA). Methods: A retrospective analysis of all consecutive patients diagnosed with ATTR-CA at the National Amyloidosis Centre between 2000-2022 identified 2371 patients with ATTR-CA. Results: Prescription of HF medications was greater among patients with a more severe cardiac phenotype, comprising beta-blockers in 55.4%, angiotensin-converting enzyme inhibitors (ACEi)/angiotensin-II receptor blockers (ARB) in 57.4%, and mineralocorticoid receptor antagonists (MRAs) in 39.0% of cases. During a median follow-up of 27.8 months (IQR 10.6-51.3), 21.7% had beta-blockers discontinued, and 32.9% had ACEi/ARB discontinued. In contrast, only 7.5% had MRAs discontinued. Propensity score-matched analysis demonstrated that treatment with MRAs was independently associated with a reduced risk of mortality in the overall population (HR 0.77 [95% CI 0.66-0.89], P<0.001) and in a pre-specified subgroup of patients with a left ventricular ejection fraction (LVEF) >40% (HR 0.75 [95% CI 0.63-0.90], P=0.002); and treatment with low-dose beta-blockers was independently associated with a reduced risk of mortality in a pre-specified subgroup of patients with a LVEF ≤40% (HR 0.61 [95% CI 0.45-0.83], P=0.002). No convincing differences were found for treatment with ACEi/ARBs. Conclusions: Conventional HF medications are currently not widely prescribed in ATTR-CA, and those that received medication had more severe cardiac disease. Beta-blockers and ACEi/ARBs were often discontinued, but low-dose beta-blockers were associated with reduced risk of mortality in patients with a LVEF ≤40%. In contrast, MRAs were rarely discontinued and were associated with reduced risk of mortality in the overall population; but these findings require confirmation in prospective randomized controlled trials.

Conventional heart failure therapy in cardiac ATTR amyloidosis / A. Ioannou, P. Massa, R.K. Patel, Y. Razvi, A. Porcari, M.U. Rauf, A. Jiang, G. Cabras, S. Filisetti, R.E. Bolhuis, F. Bandera, L. Venneri, A. Martinez-Naharro, S. Law, T. Kotecha, R. Virsinskaite, D.S. Knight, M. Emdin, A. Petrie, H. Lachmann, A. Wechelakar, M. Petrie, A. Hughes, N. Freemantle, P.N. Hawkins, C. Whelan, J.J. Mcmurray, J.D. Gillmore, M. Fontana. - In: EUROPEAN HEART JOURNAL. - ISSN 0195-668X. - (2023). [Epub ahead of print] [10.1093/eurheartj/ehad347]

Conventional heart failure therapy in cardiac ATTR amyloidosis

F. Bandera;
2023

Abstract

Background and aims: The aims of this study were to assess prescription patterns, dosages, discontinuation rates and association with prognosis of conventional heart failure (HF) medications in patients with transthyretin cardiac amyloidosis (ATTR-CA). Methods: A retrospective analysis of all consecutive patients diagnosed with ATTR-CA at the National Amyloidosis Centre between 2000-2022 identified 2371 patients with ATTR-CA. Results: Prescription of HF medications was greater among patients with a more severe cardiac phenotype, comprising beta-blockers in 55.4%, angiotensin-converting enzyme inhibitors (ACEi)/angiotensin-II receptor blockers (ARB) in 57.4%, and mineralocorticoid receptor antagonists (MRAs) in 39.0% of cases. During a median follow-up of 27.8 months (IQR 10.6-51.3), 21.7% had beta-blockers discontinued, and 32.9% had ACEi/ARB discontinued. In contrast, only 7.5% had MRAs discontinued. Propensity score-matched analysis demonstrated that treatment with MRAs was independently associated with a reduced risk of mortality in the overall population (HR 0.77 [95% CI 0.66-0.89], P<0.001) and in a pre-specified subgroup of patients with a left ventricular ejection fraction (LVEF) >40% (HR 0.75 [95% CI 0.63-0.90], P=0.002); and treatment with low-dose beta-blockers was independently associated with a reduced risk of mortality in a pre-specified subgroup of patients with a LVEF ≤40% (HR 0.61 [95% CI 0.45-0.83], P=0.002). No convincing differences were found for treatment with ACEi/ARBs. Conclusions: Conventional HF medications are currently not widely prescribed in ATTR-CA, and those that received medication had more severe cardiac disease. Beta-blockers and ACEi/ARBs were often discontinued, but low-dose beta-blockers were associated with reduced risk of mortality in patients with a LVEF ≤40%. In contrast, MRAs were rarely discontinued and were associated with reduced risk of mortality in the overall population; but these findings require confirmation in prospective randomized controlled trials.
English
Beta-blockers; Cardiac ATTR amyloidosis; Heart failure; Heart failure medications; Mineralocorticoid receptor antagonists
Settore MED/11 - Malattie dell'Apparato Cardiovascolare
Articolo
Esperti anonimi
Pubblicazione scientifica
2023
22-mag-2023
Oxford University Press
ehad347
Epub ahead of print
Periodico con rilevanza internazionale
pubmed
crossref
Aderisco
info:eu-repo/semantics/article
Conventional heart failure therapy in cardiac ATTR amyloidosis / A. Ioannou, P. Massa, R.K. Patel, Y. Razvi, A. Porcari, M.U. Rauf, A. Jiang, G. Cabras, S. Filisetti, R.E. Bolhuis, F. Bandera, L. Venneri, A. Martinez-Naharro, S. Law, T. Kotecha, R. Virsinskaite, D.S. Knight, M. Emdin, A. Petrie, H. Lachmann, A. Wechelakar, M. Petrie, A. Hughes, N. Freemantle, P.N. Hawkins, C. Whelan, J.J. Mcmurray, J.D. Gillmore, M. Fontana. - In: EUROPEAN HEART JOURNAL. - ISSN 0195-668X. - (2023). [Epub ahead of print] [10.1093/eurheartj/ehad347]
open
Prodotti della ricerca::01 - Articolo su periodico
29
262
Article (author)
Periodico con Impact Factor
A. Ioannou, P. Massa, R.K. Patel, Y. Razvi, A. Porcari, M.U. Rauf, A. Jiang, G. Cabras, S. Filisetti, R.E. Bolhuis, F. Bandera, L. Venneri, A. Martine...espandi
File in questo prodotto:
File Dimensione Formato  
ehad347.pdf

accesso aperto

Descrizione: Article
Tipologia: Post-print, accepted manuscript ecc. (versione accettata dall'editore)
Dimensione 1.3 MB
Formato Adobe PDF
1.3 MB Adobe PDF Visualizza/Apri
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/972651
Citazioni
  • ???jsp.display-item.citation.pmc??? 63
  • Scopus 120
  • ???jsp.display-item.citation.isi??? 115
  • OpenAlex ND
social impact