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.

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Journal
European Journal of Heart Failure
Published
2025-06-09
DOI
https://doi.org/10.1002/ejhf.3698
Primary Topic
Amyloidosis: Diagnosis, Treatment, Outcomes
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article
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article

Application of a Transthyretin Amyloid Cardiomyopathy Score to Heart Failure with Mildly Reduced or Preserved Ejection Fraction

Sanjiv J. Shah, Pardeep S. Jhund, Eldrin Foster Lewis, John J.V. McMurray et al.
European Journal of Heart Failure
Amyloidosis: Diagnosis, Treatment, Outcomes
article

Application of a Transthyretin Amyloid Cardiomyopathy Score to Heart Failure with Mildly Reduced or Preserved Ejection Fraction

Sanjiv J. Shah, Pardeep S. Jhund, Eldrin Foster Lewis, John J.V. McMurray, Margaret M. Redfield, Barry A. Borlaug, Marc A. Pfeffer, Brian Claggett, Scott David Solomon, Riccardo Maria Inciardi, Muthiah Vaduganathan, Omar F. AbouEzzeddine, Marianna Fontana, Akshay S. Desai, Masatoshi Minamisawa, Carolyn S.P. Lam
article en

Abstract

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.

European Journal of Heart FailureVol. 27(12)
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)
Good health and well-being
Openalex Percentile: Top 88%
Amyloidosis: Diagnosis, Treatment, Outcomes
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