TY - JOUR
T1 - Association of cardiac troponin i with disease severity and outcomes in patients with pulmonary hypertension
AU - Vélez-Martínez, Mariella
AU - Ayers, Colby
AU - Mishkin, Joseph D.
AU - Bartolome, Sonja D
AU - Garcia, Christine K
AU - Torres, Fernando
AU - Drazner, Mark H
AU - de Lemos, James A
AU - Turer, Aslan T
AU - Chin, Kelly M
N1 - Funding Information:
Kelly Chin, Sonja Bartolome, and Fernando Torres have served as a scientific advisors, consultants, and/or investigators in clinical trials for Actelion, Bayer, Geno, Gilead, Pfizer, and United Therapeutics and have received grant support from the National Institutes of Health . Fernando Torres has additionally served as a scientific advisor, consultant, and/or investigator in clinical trials for Glaxo Smith and Novartis. James de Lemos has received grant support from Roche and Abbott Diagnostics . The remaining authors have no conflicts of interest to disclose.
PY - 2013/6/15
Y1 - 2013/6/15
N2 - Previous studies have identified cardiac troponin I (cTnI) as an important marker in pulmonary hypertension (PH) prognosis. However, traditional assays are limited by poor sensitivity, even among patients at high risk. cTnI was measured in 255 PH patients using a new highly sensitive (hs) assay. Other measures included demographics, creatinine, 6-minute walk distance, hemodynamics, cardiac magnetic resonance imaging, and B-type natriuretic peptide level. The association between cTnI and survival was assessed using Kaplan-Meier analysis and Cox regression. cTnI was detectable with the hs assay in 95% of the patients with a median level of 6.9 pg/ml (IQR 2.7-12.6 pg/ml). Higher cTnI levels associated with higher levels of B-type natriuretic peptide, shorter 6-minute walk distance, and more severe hemodynamic and cardiac magnetic resonance imaging abnormalities. During a median follow-up of 3.5 years, 60 individuals died. Unadjusted event rates increased across higher cTnI quartiles (3, 5, 13, 17 events/100 person-years, respectively, p trend = 0.002). cTnI in the fourth (vs first) quartile remained associated with death in a final stepwise multivariable model that included clinical variables and hemodynamics (adjusted hazard ratio 5.3, 95% confidence interval 1.8-15.6). In conclusion, cTnI levels, detectable with a novel hs assay, identify patients with PH who have more severe hemodynamic and cardiac structural abnormalities and provide novel and independent prognostic information. This hs assay has the potential to detect more at-risk patients and improve current risk-stratification algorithms.
AB - Previous studies have identified cardiac troponin I (cTnI) as an important marker in pulmonary hypertension (PH) prognosis. However, traditional assays are limited by poor sensitivity, even among patients at high risk. cTnI was measured in 255 PH patients using a new highly sensitive (hs) assay. Other measures included demographics, creatinine, 6-minute walk distance, hemodynamics, cardiac magnetic resonance imaging, and B-type natriuretic peptide level. The association between cTnI and survival was assessed using Kaplan-Meier analysis and Cox regression. cTnI was detectable with the hs assay in 95% of the patients with a median level of 6.9 pg/ml (IQR 2.7-12.6 pg/ml). Higher cTnI levels associated with higher levels of B-type natriuretic peptide, shorter 6-minute walk distance, and more severe hemodynamic and cardiac magnetic resonance imaging abnormalities. During a median follow-up of 3.5 years, 60 individuals died. Unadjusted event rates increased across higher cTnI quartiles (3, 5, 13, 17 events/100 person-years, respectively, p trend = 0.002). cTnI in the fourth (vs first) quartile remained associated with death in a final stepwise multivariable model that included clinical variables and hemodynamics (adjusted hazard ratio 5.3, 95% confidence interval 1.8-15.6). In conclusion, cTnI levels, detectable with a novel hs assay, identify patients with PH who have more severe hemodynamic and cardiac structural abnormalities and provide novel and independent prognostic information. This hs assay has the potential to detect more at-risk patients and improve current risk-stratification algorithms.
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U2 - 10.1016/j.amjcard.2013.02.036
DO - 10.1016/j.amjcard.2013.02.036
M3 - Article
C2 - 23540547
AN - SCOPUS:84878843260
SN - 0002-9149
VL - 111
SP - 1812
EP - 1817
JO - American Journal of Cardiology
JF - American Journal of Cardiology
IS - 12
ER -