Your browser doesn't support javascript.
loading
Stratifying Disease Progression in Patients With Cardiac ATTR Amyloidosis.
Ioannou, Adam; Cappelli, Francesco; Emdin, Michele; Nitsche, Christian; Longhi, Simone; Masri, Ahmad; Cipriani, Alberto; Zampieri, Mattia; Colio, Federica; Poledniczek, Michael; Porcari, Aldostefano; Razvi, Yousuf; Aimo, Alberto; Vergaro, Giuseppe; De Michieli, Laura; Rauf, Muhammad U; Patel, Rishi K; Villanueva, Eugenia; Lustig, Yael; Venneri, Lucia; Martinez-Naharro, Ana; Lachmann, Helen; Wechalekar, Ashutosh; Whelan, Carol; Petrie, Aviva; Hawkins, Philip N; Solomon, Scott; Gillmore, Julian D; Fontana, Marianna.
Affiliation
  • Ioannou A; National Amyloidosis Centre, University College London, London, United Kingdom.
  • Cappelli F; Tuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy.
  • Emdin M; Health Science Interdisciplinary Center, Scuola Superiore Sant'Anna, Pisa, Italy; Fondazione Toscana Gabriele Monasterio, Pisa, Italy.
  • Nitsche C; Division of Cardiology, Department of Internal Medicine, Medical University of Vienna, Vienna, Austria.
  • Longhi S; Cardiology Unit, Cardiac Thoracic and Vascular Department, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
  • Masri A; OHSU Center for Hypertrophic Cardiomyopathy and Amyloidosis, Portland, Oregon, USA.
  • Cipriani A; Department of Cardiac, Thoracic and Vascular Sciences and Public Health, University of Padua, Padua, Italy; Cardiology Unit, University Hospital Padua, Padua, Italy.
  • Zampieri M; Tuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy.
  • Colio F; Tuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy.
  • Poledniczek M; Division of Cardiology, Department of Internal Medicine, Medical University of Vienna, Vienna, Austria.
  • Porcari A; National Amyloidosis Centre, University College London, London, United Kingdom; Center for Diagnosis and Treatment of Cardiomyopathies, Cardiovascular Department, Azienda Sanitaria Universitaria Giuliano-Isontina (ASUGI), University of Trieste, Trieste, Italy.
  • Razvi Y; National Amyloidosis Centre, University College London, London, United Kingdom.
  • Aimo A; Health Science Interdisciplinary Center, Scuola Superiore Sant'Anna, Pisa, Italy; Fondazione Toscana Gabriele Monasterio, Pisa, Italy.
  • Vergaro G; Health Science Interdisciplinary Center, Scuola Superiore Sant'Anna, Pisa, Italy; Fondazione Toscana Gabriele Monasterio, Pisa, Italy.
  • De Michieli L; Department of Cardiac, Thoracic and Vascular Sciences and Public Health, University of Padua, Padua, Italy.
  • Rauf MU; National Amyloidosis Centre, University College London, London, United Kingdom.
  • Patel RK; National Amyloidosis Centre, University College London, London, United Kingdom.
  • Villanueva E; National Amyloidosis Centre, University College London, London, United Kingdom.
  • Lustig Y; National Amyloidosis Centre, University College London, London, United Kingdom.
  • Venneri L; National Amyloidosis Centre, University College London, London, United Kingdom.
  • Martinez-Naharro A; National Amyloidosis Centre, University College London, London, United Kingdom.
  • Lachmann H; National Amyloidosis Centre, University College London, London, United Kingdom.
  • Wechalekar A; National Amyloidosis Centre, University College London, London, United Kingdom.
  • Whelan C; National Amyloidosis Centre, University College London, London, United Kingdom.
  • Petrie A; University College London, Biostatistics Unit, UCL Eastman Dental Institute, London, United Kingdom.
  • Hawkins PN; National Amyloidosis Centre, University College London, London, United Kingdom.
  • Solomon S; Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Gillmore JD; National Amyloidosis Centre, University College London, London, United Kingdom.
  • Fontana M; National Amyloidosis Centre, University College London, London, United Kingdom. Electronic address: m.fontana@ucl.ac.uk.
J Am Coll Cardiol ; 2024 Mar 01.
Article in En | MEDLINE | ID: mdl-38530684
ABSTRACT

BACKGROUND:

Transthyretin cardiac amyloidosis (ATTR-CA) is a progressive cardiomyopathy. The clinical course varies among individuals and there are no established measures to assess disease progression.

OBJECTIVES:

The goal of this study was to assess the prognostic importance of an increase in N-terminal pro-B-type natriuretic peptide (NT-proBNP) and outpatient diuretic intensification (ODI) as markers of disease progression in a large cohort of patients with ATTR-CA.

METHODS:

We evaluated landmark survival analysis based on worsening of NT-proBNP and requirement for ODI between time of diagnosis and a 1-year visit, and subsequent mortality in 2,275 patients with ATTR-CA from 7 specialist centers. The variables were developed in the National Amyloidosis Centre (NAC) cohort (n = 1,598) and validated in the external cohort from the remaining centers (n = 677).

RESULTS:

Between baseline and 1-year visits, 551 (34.5%) NAC patients and 204 (30.1%) patients in the external validation cohort experienced NT-proBNP progression (NT-proBNP increase >700 ng/L and >30%), which was associated with mortality (NAC cohort HR 1.82; 95% CI 1.57-2.10; P < 0.001; validation cohort HR 1.75; 95% CI 1.32-2.33; P < 0.001). At 1 year, 451 (28.2%) NAC patients and 301 (44.5%) patients in the external validation cohort experienced ODI, which was associated with mortality (NAC cohort HR 1.88; 95% CI 1.62-2.18; P < 0.001; validation cohort HR 2.05; 95% CI 1.53-2.74; P < 0.001). When compared with patients with a stable NT-proBNP and stable diuretic dose, a higher risk of mortality was observed in those experiencing either NT-proBNP progression or ODI (NAC cohort HR 1.93; 95% CI 1.65-2.27; P < 0.001; validation cohort HR 1.94; 95% CI 1.36-2.77; P < 0.001), and those experiencing both NT-proBNP progression and ODI (NAC cohort HR 2.98; 95% CI 2.42-3.67; P < 0.001; validation cohort HR 3.23; 95% CI 2.17-4.79; P < 0.001).

CONCLUSIONS:

NT-proBNP progression and ODI are frequent and consistently associated with an increased risk of mortality. Combining both variables produces a simple, universally applicable model that detects disease progression in ATTR-CA.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Am Coll Cardiol Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Am Coll Cardiol Year: 2024 Document type: Article Affiliation country: