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American Heart Association

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Final ID: MDP861

Renal outcomes in transthyretin cardiac amyloidosis

Abstract Body (Do not enter title and authors here): Background: Transthyretin cardiac amyloidosis (ATTR-CA) is a progressive cardiomyopathy that commonly presents with concomitant chronic kidney disease. Impaired renal function is associated with worse outcomes, but the prognostic value of changes in renal function over time are yet to be defined.
Objectives: This study aimed to assess the prognostic importance of a decline in estimated glomerular filtration rate (eGFR) as a marker of renal progression in a large cohort of patients with ATTR-CA.
Methods: A retrospective analysis of 2001 patients diagnosed with ATTR-CA at the National Amyloidosis Centre (NAC) who underwent a baseline and follow-up eGFR assessment at 1-year between 2000-2024.
Results: Between baseline and 1-year visits, 208(10.4%) patients experienced renal progression (defined as a decrease in eGFR of >30%). Renal progression was associated with a 2.4-fold higher risk of mortality (HR=2.37,95%CI[1.91-2.94],P<0.001) and the risk was similar across the 3 genotypes (interaction P=0.972) and the 3 NAC disease stages (interaction P=0.172). Deterioration of the cardiorenal axis is tracked through a biomarker progression score composed of NT-proBNP progression (defined as an increase of >700ng/L and >30%) and renal progression. When compared with patients with a stable NT-proBNP and eGFR, a higher risk of mortality was observed in patients experiencing either NT-proBNP or renal progression (HR=2.02,95%CI[1.70-2.40],P<0.001) and those experiencing both NT-proBNP and renal progression (HR=3.77,95%CI[2.84-5.00],P<0.001).
Conclusions: Renal progression is frequent and consistently associated with an increased risk of mortality. Combining renal and NT-proBNP progression produces a biomarker progression score that reflects worsening of the cardiorenal axis and identifies patients at the highest risk.
  • Ioannou, Adam  ( University College London , London , United Kingdom )
  • Razvi, Yousuf  ( Royal Free Hospital , London , London , United Kingdom )
  • Porcari, Aldostefano  ( Royal Free Hospital , London , London , United Kingdom )
  • Rauf, Muhammad  ( Royal Free Hospital , London , London , United Kingdom )
  • Martinez-naharro, Ana  ( Royal Free Hospital , London , London , United Kingdom )
  • Venneri, Lucia  ( Royal Free Hospital , London , London , United Kingdom )
  • Hawkins, Philip  ( National Amyloidosis Centre , London , United Kingdom )
  • Gillmore, Julian  ( UCL Centre for Amyloidosis , London , United Kingdom )
  • Fontana, Marianna  ( University College London , London , United Kingdom )
  • Author Disclosures:
    Adam Ioannou: DO NOT have relevant financial relationships | Yousuf Razvi: DO NOT have relevant financial relationships | Aldostefano Porcari: No Answer | Muhammad Rauf: DO NOT have relevant financial relationships | Ana Martinez-Naharro: No Answer | Lucia Venneri: No Answer | Philip Hawkins: DO NOT have relevant financial relationships | Julian Gillmore: DO have relevant financial relationships ; Consultant:Alnylam, ATTRalus, AstraZeneca, Bridgebio, Lycia, Intellia, Pfizer:Active (exists now) | Marianna Fontana: DO have relevant financial relationships ; Consultant:Dr. Fontana reports consultancy/advisory boards for Alnylam, Alexion/Caelum Biosciences, Astrazeneca, Bridgbio/Eidos, Prothena, Attralus, Intellia Therapeutics, Ionis Pharmaceuticals, Cardior, Lexeo Therapeutics, Janssen Pharmaceuticals, Prothena, Pfizer, Novonordisk, Bayer, Mycardium. Research grants from: Alnylam, Bridgbio, Astrazeneca, Pfizer. Salary from British Heart Foundation Intermediate Fellowship. Share options in LexeoTherapeutics and shares in Mycardium.:Active (exists now)
Meeting Info:

Scientific Sessions 2024

2024

Chicago, Illinois

Session Info:

Cardiac Amyloidosis 2024: Advances in Prognostication and Management

Sunday, 11/17/2024 , 11:10AM - 12:35PM

Moderated Digital Poster Session

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