Biomarkers and Prediction of Prognosis in Transthyretin-Related Cardiac Amyloidosis: Direct Comparison of Two Staging Systems.


Journal

The Canadian journal of cardiology
ISSN: 1916-7075
Titre abrégé: Can J Cardiol
Pays: England
ID NLM: 8510280

Informations de publication

Date de publication:
03 2020
Historique:
received: 04 09 2019
revised: 13 12 2019
accepted: 22 12 2019
entrez: 9 3 2020
pubmed: 9 3 2020
medline: 23 10 2020
Statut: ppublish

Résumé

The severity of heart disease varies widely among patients with transthyretin-related cardiac amyloidosis (ATTR-CA) at presentation, and availability of tools able to predict prognosis is essential for clinical and research purposes. Currently, two biomarker-based staging systems are available. The aim of this study was to compare their predictive performance. A total of 175 patients diagnosed with ATTR-CA (133 wild-type and 42 hereditary) were stratified into different stages based on 2 systems: the first system included N-terminal pro-B-type natriuretic peptide (NT-proBNP) and estimated glomerular filtration rate (eGFR), and the second one included NT-proBNP and troponin I (TnI). Survival estimates and age-adjusted survival for all-cause mortality were analysed over a median follow-up of 27 months (interquartile range 16-43 months). Predictive performance was more accurate when NT-proBNP and eGFR were used, resulting in effective survival stratification: 64.4 months for stage 1, 44.6 months for stage 2, and 20.5 months for stage 3 (P < 0.01 for stages 1 vs 2; P < 0.0001 for stages 1 vs 3; P < 0.0001 stages 2 vs 3). The combination of NT-proBNP and TnI was unable to effectively differentiate survival: 64.5 months for stage 1, 50.9 months for stage 2, and 27.3 months for stage 3 (P = 0.223 for stages 1 vs 2; P < 0.0001 for stages 1 vs 3; P < 0.0001 for stages 2 vs 3). The same results were seen after age adjustment. A staging system using NT-proBNP and eGFR had better prognostic accuracy for ATTR-CA patients compared with one using NTproBNP and TnI.

Sections du résumé

BACKGROUND
The severity of heart disease varies widely among patients with transthyretin-related cardiac amyloidosis (ATTR-CA) at presentation, and availability of tools able to predict prognosis is essential for clinical and research purposes. Currently, two biomarker-based staging systems are available. The aim of this study was to compare their predictive performance.
METHODS
A total of 175 patients diagnosed with ATTR-CA (133 wild-type and 42 hereditary) were stratified into different stages based on 2 systems: the first system included N-terminal pro-B-type natriuretic peptide (NT-proBNP) and estimated glomerular filtration rate (eGFR), and the second one included NT-proBNP and troponin I (TnI). Survival estimates and age-adjusted survival for all-cause mortality were analysed over a median follow-up of 27 months (interquartile range 16-43 months).
RESULTS
Predictive performance was more accurate when NT-proBNP and eGFR were used, resulting in effective survival stratification: 64.4 months for stage 1, 44.6 months for stage 2, and 20.5 months for stage 3 (P < 0.01 for stages 1 vs 2; P < 0.0001 for stages 1 vs 3; P < 0.0001 stages 2 vs 3). The combination of NT-proBNP and TnI was unable to effectively differentiate survival: 64.5 months for stage 1, 50.9 months for stage 2, and 27.3 months for stage 3 (P = 0.223 for stages 1 vs 2; P < 0.0001 for stages 1 vs 3; P < 0.0001 for stages 2 vs 3). The same results were seen after age adjustment.
CONCLUSIONS
A staging system using NT-proBNP and eGFR had better prognostic accuracy for ATTR-CA patients compared with one using NTproBNP and TnI.

Identifiants

pubmed: 32145869
pii: S0828-282X(19)31546-6
doi: 10.1016/j.cjca.2019.12.020
pii:
doi:

Substances chimiques

Biomarkers 0
Peptide Fragments 0
Troponin I 0
pro-brain natriuretic peptide (1-76) 0
Natriuretic Peptide, Brain 114471-18-0

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

424-431

Informations de copyright

Copyright © 2019 Canadian Cardiovascular Society. Published by Elsevier Inc. All rights reserved.

Auteurs

Francesco Cappelli (F)

Tuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy; Division of Interventional Structural Cardiology, Cardiothoracovascular Department, Careggi University Hospital, Florence, Italy. Electronic address: cappellif@aou-careggi.toscana.it.

Raffaele Martone (R)

Tuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy.

Martina Gabriele (M)

Tuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy.

Giulia Taborchi (G)

Tuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy.

Sofia Morini (S)

Tuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy.

Elisa Vignini (E)

Tuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy.

Marco Allinovi (M)

Tuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy.

Massimo Di Gioia (M)

Tuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy.

Simone Bartolini (S)

Tuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy; Cardiology Department, Azienda Sanitaria Firenze, Florence, Italy.

Carlo Di Mario (C)

Division of Interventional Structural Cardiology, Cardiothoracovascular Department, Careggi University Hospital, Florence, Italy.

Federico Perfetto (F)

Tuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy.

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