Biomarkers strongly predicted cause-specific mortality in atrial fibrillation, with a doubling of troponin T associated with sudden cardiac death (HR 1.48; P<0.001).
RCT (n=14,798)
randomized
Do biomarkers (troponin T, GDF-15, NT-proBNP, IL-6) predict specific causes of death in anticoagulated patients with atrial fibrillation?
Specific biomarkers (troponin T, NT-proBNP, GDF-15) strongly predict distinct causes of death in anticoagulated patients with atrial fibrillation, improving risk discrimination beyond clinical variables.
Effect estimate: HR 1.48
p-value: p=<0.001
BACKGROUND: Atrial fibrillation is associated with an increased risk of death. High-sensitivity troponin T, growth differentiation factor-15, NT-proBNP (N-terminal pro-B-type natriuretic peptide), and interleukin-6 levels are predictive of cardiovascular events and total cardiovascular death in anticoagulated patients with atrial fibrillation. The prognostic utility of these biomarkers for cause-specific death is unknown. METHODS: The ARISTOTLE trial (Apixaban for the Prevention of Stroke in Subjects With Atrial Fibrillation) randomized 18 201 patients with atrial fibrillation to apixaban or warfarin. Biomarkers were measured at randomization in 14 798 patients (1.9 years median follow-up). Cox models were used to identify clinical variables and biomarkers independently associated with each specific cause of death. RESULTS: In total, 1272 patients died: 652 (51%) cardiovascular, 32 (3%) bleeding, and 588 (46%) noncardiovascular/nonbleeding deaths. Among cardiovascular deaths, 255 (39%) were sudden cardiac deaths, 168 (26%) heart failure deaths, and 106 (16%) stroke/systemic embolism deaths. Biomarkers were the strongest predictors of cause-specific death: a doubling of troponin T was most strongly associated with sudden death (hazard ratio HR, 1.48; P0.001) followed by troponin T (HR, 1.45; P<0.0029) were the most predictive for stroke/ systemic embolism death. Adding all biomarkers to clinical variables improved discrimination for each cause-specific death. CONCLUSIONS: Biomarkers were some of the strongest predictors of cause-specific death and may improve the ability to discriminate among patients' risks for different causes of death. These data suggest a potential role of biomarkers for the identification of patients at risk for different causes of death in patients anticoagulated for atrial fibrillation. CLINICAL TRIAL REGISTRATION: URL: https://www.clinicaltrials.gov . Unique identifier: NCT00412984.
Sharma et al. (Tue,) conducted a rct in Atrial fibrillation (n=14,798). Apixaban vs. Warfarin was evaluated on Sudden cardiac death (per doubling of troponin T) (HR 1.48, p=<0.001). Biomarkers strongly predicted cause-specific mortality in atrial fibrillation, with a doubling of troponin T associated with sudden cardiac death (HR 1.48; P<0.001).