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Published on: February 26, 2013
Risk prediction of atrial fibrillation and its complications in the community using hs troponin I
Christin S Börschel1,2, Bastiaan Geelhoed1,2, Teemu Niiranen3,4,5
1Department of Cardiology, University Heart and Vascular Centre Hamburg-Eppendorf, Hamburg, Germany.
Insights
High-sensitivity troponin I (hsTnI) does not improve atrial fibrillation (AF) prediction beyond traditional risk factors. However, elevated hsTnI indicates increased risk for heart failure and mortality in AF patients.
Area of Science:
- Cardiology
- Biomarker research
- Epidemiology
Background:
- Atrial fibrillation (AF) incidence is rising, with traditional cardiovascular risk factors (CVRF) insufficient to explain all cases.
- Blood-based biomarkers like high-sensitivity troponin I (hsTnI) may offer insights into unexplained AF development.
- Investigating novel biomarkers is crucial for improving AF risk stratification.
Purpose of the Study:
- To evaluate the predictive capability of hsTnI for incident AF.
- To compare hsTnI's predictive performance against established CVRF and biomarkers.
- To explore associations between hsTnI and related cardiovascular outcomes.
Main Methods:
- Analysis of 45,298 participants from European community cohorts.
- Prospective investigation of hsTnI levels for predicting incident AF over a median follow-up of 7.7 years.
- Multivariable Cox proportional hazards models used to assess associations, adjusting for CVRF and other biomarkers.
Main Results:
- Individuals in the highest hsTnI quartile (≥4.2 ng/L) had a 3.91-fold increased risk of developing AF.
- A significant association was observed between hsTnI and AF incidence (HR per SD increase 1.08, p=0.03).
- hsTnI improved model discrimination slightly (C-index 0.811 vs. 0.813, p<0.01) and was linked to heart failure and mortality.
Conclusions:
- hsTnI, a marker of myocardial injury, does not enhance AF incidence prediction beyond CVRF and NT-proBNP.
- Elevated hsTnI is associated with heart failure and mortality, suggesting subclinical cardiovascular impairment.
- hsTnI may serve as an indicator of underlying cardiovascular disease burden rather than a direct predictor of AF onset.
Aims:
Atrial fibrillation (AF) is becoming increasingly common. Traditional cardiovascular risk factors (CVRF) do not explain all AF cases. Blood-based biomarkers reflecting cardiac injury such as high-sensitivity troponin I (hsTnI) may help close this gap.
Methods:
We investigated the predictive ability of hsTnI for incident AF in 45,298 participants (median age 51.4 years, 45.0% men) across European community cohorts in comparison to CVRF and established biomarkers (C-reactive protein, N-terminal pro B-type natriuretic peptide).
Results:
During a median follow-up of 7.7 years, 1734 (3.8%) participants developed AF. Those in the highest hsTnI quarter (≥4.2 ng/L) had a 3.91-fold (95% confidence interval (CI) 3.30, 4.63; p < .01) risk for developing AF compared to the lowest quarter (<1.4 ng/L). In multivariable-adjusted Cox proportional hazards models a statistically significant association was seen between hsTnI and AF (hazard ratio (HR) per 1 standard deviation (SD) increase in log10(hsTnI) 1.08; 95% CI 1.01, 1.16; p = .03). Inclusion of hsTnI did improve model discrimination (C-index CVRF 0.811 vs. C-index CVRF and hsTnI 0.813; p < .01). Higher hsTnI concentrations were associated with heart failure (HR per SD 1.37; 95% CI 1.12, 1.68; p < .01) and overall mortality (HR per SD 1.24; 95% CI 1.09, 1.41; p < .01).
Conclusion:
hsTnI as a biomarker of myocardial injury does not improve prediction of AF incidence beyond classical CVRF and NT-proBNP. However, it is associated with the AF-related disease heart failure and mortality likely reflecting underlying subclinical cardiovascular impairment.
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