Application of a Transthyretin Amyloid Cardiomyopathy Score to Heart Failure with Mildly Reduced or Preserved Ejection Fraction
Aims The safety and efficacy of heart failure (HF)-directed medical therapy among patients who might be considered for further diagnostic evaluation to rule out transthyretin amyloid cardiomyopathy (ATTR-CM) is largely unknown. Methods and results We applied a previously validated ATTR-CM screening score in patients with HF and mildly reduced or preserved ejection fraction (HFmrEF/HFpEF) and assessed treatment effect of sodium–glucose cotransporter 2 inhibitors (SGLT2i), angiotensin receptor–neprilysin inhibitor (ARNI) and mineralocorticoid receptor antagonists (MRAs) based on their score-based ATTR-CM risk, from the DELIVER, PARAGON-HF and TOPCAT Americas trials. We applied a re-derived five-variable modified ATTR-CM score (range −1 to 9) which included age, male sex, hypertension, left ventricular ejection fraction <60%, posterior wall thickness ≥12 mm. We calculated the modified ATTR-CM risk score from DELIVER (available in 4085 patients; 65%), PARAGON-HF (4067; 85%) and TOPCAT Americas (645; 37%). Median scores were 5 (interquartile range [IQR] 4–6) in DELIVER and 4 (IQR 3–6) in both PARAGON-HF and TOPCAT Americas. Higher modified ATTR-CM score was associated with greater risk of the primary endpoint for each trial. However, ATTR-CM risk score did not significantly modify the treatment effect of dapagliflozin (pinteraction = 0.85), sacubitril/valsartan (pinteraction = 0.10), or spironolactone (pinteraction = 0.57). The safety profile of each drug was consistent irrespective of modified ATTR-CM score. Conclusions Among three large contemporary HFmrEF/HFpEF trials, the safety and efficacy of SGLT2i, ARNI, and MRA were not modified in patients at risk for ATTR-CM, suggesting that the diagnostic process to rule out amyloidosis should not necessarily delay the introduction of conventional HF medical therapies. Clinical Trial Registration: ClinicalTrials.gov Identifiers: DELIVER, NCT03619213; PARAGON-HF, NCT01920711; TOPCAT, NCT00094302.
Authors
- Sanjiv J. Shah (ORCID: https://orcid.org/0000-0002-5655-8201)
- Pardeep S. Jhund (ORCID: https://orcid.org/0000-0003-4306-5317)
- Eldrin Foster Lewis (ORCID: https://orcid.org/0000-0002-5147-9512)
- John J.V. McMurray (ORCID: https://orcid.org/0000-0002-6317-3975)
- Margaret M. Redfield (ORCID: https://orcid.org/0000-0002-0946-7518)
- Barry A. Borlaug (ORCID: https://orcid.org/0000-0001-9375-0596)
- Marc A. Pfeffer (ORCID: https://orcid.org/0000-0003-3876-7568)
- Brian Claggett
- Scott David Solomon (ORCID: https://orcid.org/0000-0003-3698-9597)
- Riccardo Maria Inciardi (ORCID: https://orcid.org/0000-0003-4846-8529)
- Muthiah Vaduganathan (ORCID: https://orcid.org/0000-0003-0885-1953)
- Omar F. AbouEzzeddine (ORCID: https://orcid.org/0000-0003-3256-3660)
- Marianna Fontana
- Akshay S. Desai
- Masatoshi Minamisawa
- Carolyn S.P. Lam
Institutions
- Northwestern University (US)
- Brigham and Women's Hospital (US)
- Mayo Clinic (US)
- Harvard University (US)
- National University of Singapore (SG)
- The Royal Free Hospital (GB)
- Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia (IT)
- National University Heart Centre Singapore (SG)
- Mayo Clinic in Arizona (US)
- Shinshu University Hospital (JP)
- Mayo Clinic in Florida (US)
- National Heart Centre Singapore (SG)
- University College London (GB)
- University of Glasgow (GB)
- Stanford University (US)
Publication Details
- Journal
- European Journal of Heart Failure
- Published
- 2025-06-09
- DOI
- https://doi.org/10.1002/ejhf.3698
- Primary Topic
- Amyloidosis: Diagnosis, Treatment, Outcomes
- Type
- article
- Field-Weighted Citation Impact
- 0.00