Key result
Rising or persistently high hsTnT, NT-proBNP, and GDF-15 are linked to higher HF hospitalization or death.
Why the study?
Cardiac functional and structural remodelling in AF contributes to HF development, and circulating biomarkers may reflect these cardiac alterations.
Do serial measurements of hsTnT, NT-proBNP, and GDF-15 predict hospitalization for heart failure or heart failure death in patients with atrial fibrillation?
RCT (n=21,105)
Do serial measurements of hsTnT, NT-proBNP, and GDF-15 predict hospitalization for heart failure or heart failure death in patients with atrial fibrillation?
p-value: p=<0.001
Serial measurements of hsTnT, NT-proBNP, and GDF-15 can identify patients with atrial fibrillation at high risk for heart failure hospitalization or death, regardless of baseline heart failure history or ejection fraction.
Serial biomarker trajectories may stratify HF risk in AF; leaves open whether monitoring improves outcomes or warrants intervention.
AIMS: Cardiac functional and structural remodelling in patients with atrial fibrillation (AF) contributes to development of heart failure (HF) as their major cardiovascular comorbidity. Circulating biomarkers may reflect these cardiac alterations. METHODS AND RESULTS: ENGAGE AF-TIMI 48 was a randomized trial of edoxaban versus warfarin in 21 105 patients with AF. We performed a nested biomarker study, analysing high-sensitivity troponin T (hsTnT, n = 8705), N-terminal pro-B-type natriuretic peptide (NT-proBNP, n = 8765), and growth differentiation factor-15 (GDF-15, n = 8705) at baseline and 12 months. Of the biomarker cohort, 5207 had a history of HF, among whom 3996 had known ejection fraction (EF): 926 with reduced EF (HFrEF; ≤40%), 1043 with mildly reduced EF (HFmrEF; 40-49%), and 2027 with preserved EF (HFpEF; ≥50%). Elevated baseline hsTnT, NT-proBNP, and GDF-15 were associated with higher risk of hospitalization for HF (HHF) or HF death overall and in subpopulations defined by HF history and EF (p < 0.001 for each). These associations of outcome with each biomarker were consistent regardless of a history of HF or EF (p-interaction >0.05 for each). Patients who had an increase in or had persistently elevated values in any of the three biomarkers over 12 months were at higher risk for HHF or HF death in the overall population (p < 0.001 for each biomarker and category). CONCLUSION: Serial measurement of hsTnT, NT-proBNP, and GDF-15 revealed that higher baseline values, and increasing or persistently elevated values over 1 year are associated with higher risk of HF outcomes in patients with AF regardless of HF history or HF phenotype based on EF. CLINICAL TRIAL REGISTRATION: ClinicalTrials.gov unique identifier NCT00781391.
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Oyama et al. (2023) conducted an RCT in Atrial fibrillation (n=21,105). Serial measurement of hsTnT, NT-proBNP, and GDF-15 was evaluated on Hospitalization for HF (HHF) or HF death (p=<0.001). Elevated baseline and persistently elevated or increasing levels of hsTnT, NT-proBNP, and GDF-15 over 12 months were associated with a higher risk of HF hospitalization or HF death (p < 0.001).
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