TY - JOUR
T1 - Predictors of incident heart failure in patients after an acute coronary syndrome
T2 - The LIPID heart failure risk-prediction model
AU - Driscoll, Andrea
AU - Barnes, Elizabeth H
AU - Blankenberg, Stefan
AU - Colquhoun, David M.
AU - Hunt, David
AU - Nestel, Paul John
AU - Stewart, Ralph A H
AU - West, Malcolm J
AU - White, Harvey D
AU - Simes, R John
AU - Tonkin, Andrew
PY - 2017/12/1
Y1 - 2017/12/1
N2 - Background: Coronary heart disease is a major cause of heart failure. Availability of risk-prediction models that include both clinical parameters and biomarkers is limited. We aimed to develop such a model for prediction of incident heart failure. Methods: A multivariable risk-factor model was developed for prediction of first occurrence of heart failure death or hospitalization. A simplified risk score was derived that enabled subjects to be grouped into categories of 5-year risk varying from <. 5% to >. 20%. Results: Among 7101 patients from the LIPID study (84% male), with median age 61years (interquartile range 55-67years), 558 (8%) died or were hospitalized because of heart failure. Older age, history of claudication or diabetes mellitus, body mass index>30kg/m2, LDL-cholesterol >2.5mmol/L, heart rate>70 beats/min, white blood cell count, and the nature of the qualifying acute coronary syndrome (myocardial infarction or unstable angina) were associated with an increase in heart failure events. Coronary revascularization was associated with a lower event rate. Incident heart failure increased with higher concentrations of B-type natriuretic peptide >50ng/L, cystatin C>0.93nmol/L, D-dimer >273nmol/L, high-sensitivity C-reactive protein >4.8nmol/L, and sensitive troponin I >0.018μg/L. Addition of biomarkers to the clinical risk model improved the model's C statistic from 0.73 to 0.77. The net reclassification improvement incorporating biomarkers into the clinical model using categories of 5-year risk was 23%. Conclusion: Adding a multibiomarker panel to conventional parameters markedly improved discrimination and risk classification for future heart failure events.
AB - Background: Coronary heart disease is a major cause of heart failure. Availability of risk-prediction models that include both clinical parameters and biomarkers is limited. We aimed to develop such a model for prediction of incident heart failure. Methods: A multivariable risk-factor model was developed for prediction of first occurrence of heart failure death or hospitalization. A simplified risk score was derived that enabled subjects to be grouped into categories of 5-year risk varying from <. 5% to >. 20%. Results: Among 7101 patients from the LIPID study (84% male), with median age 61years (interquartile range 55-67years), 558 (8%) died or were hospitalized because of heart failure. Older age, history of claudication or diabetes mellitus, body mass index>30kg/m2, LDL-cholesterol >2.5mmol/L, heart rate>70 beats/min, white blood cell count, and the nature of the qualifying acute coronary syndrome (myocardial infarction or unstable angina) were associated with an increase in heart failure events. Coronary revascularization was associated with a lower event rate. Incident heart failure increased with higher concentrations of B-type natriuretic peptide >50ng/L, cystatin C>0.93nmol/L, D-dimer >273nmol/L, high-sensitivity C-reactive protein >4.8nmol/L, and sensitive troponin I >0.018μg/L. Addition of biomarkers to the clinical risk model improved the model's C statistic from 0.73 to 0.77. The net reclassification improvement incorporating biomarkers into the clinical model using categories of 5-year risk was 23%. Conclusion: Adding a multibiomarker panel to conventional parameters markedly improved discrimination and risk classification for future heart failure events.
KW - Acute coronary heart disease
KW - Biomarkers
KW - Heart failure
KW - Risk-prediction model
UR - http://www.scopus.com/inward/record.url?scp=85024104205&partnerID=8YFLogxK
U2 - 10.1016/j.ijcard.2017.06.098
DO - 10.1016/j.ijcard.2017.06.098
M3 - Article
AN - SCOPUS:85024104205
SN - 0167-5273
VL - 248
SP - 361
EP - 368
JO - International Journal of Cardiology
JF - International Journal of Cardiology
ER -