Key result
Dapagliflozin, sacubitril/valsartan, and spironolactone maintain consistent efficacy across ATTR-CM risk scores.
Why the study?
Does the ATTR-CM risk score modify the treatment effect of dapagliflozin, sacubitril/valsartan, or spironolactone in patients with HFmrEF/HFpEF?
RCT (n=8,797)
Yes
Does the ATTR-CM risk score modify the treatment effect of dapagliflozin, sacubitril/valsartan, or spironolactone in patients with HFmrEF/HFpEF?
Answers are grounded in this paper and cite their sources.
The efficacy and safety of dapagliflozin, sacubitril/valsartan, and spironolactone in HFmrEF/HFpEF are not modified by ATTR-CM risk, suggesting conventional HF therapies should not be delayed while ruling out amyloidosis.
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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Inciardi et al. (2025) conducted an RCT in Heart failure with mildly reduced or preserved ejection fraction (HFmrEF/HFpEF) (n=8,797). SGLT2i (dapagliflozin), ARNI (sacubitril/valsartan), and MRAs (spironolactone) was evaluated on Primary endpoint for each trial. Dapagliflozin, sacubitril/valsartan, and spironolactone maintained consistent efficacy irrespective of ATTR-CM risk score (p-interaction 0.85, 0.10, and 0.57, respectively).
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