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Enzymes and Protein Markers |
1
Department of Pathology, University of Maryland School of Medicine, Baltimore, MD.
2
Duke Clinical Research Institute, Durham, NC.
3
Department of Medicine, University of Edmonton,
Edmonton, AB, Canada.
4
Medizinische Klinik II, Medizinische
Universität Lübeck, Lübeck, Germany.
5
The Cleveland Clinic Foundation, Cleveland, OH.
a Address correspondence to this author at: Clinical Pathology, University of Maryland Medical Center, 22 South Greene St., Baltimore, MD 21201. Fax 410-328-5880; e-mail rchriste{at}umms001.ab.umd.edu.
We compared cardiac troponins T (cTnT) and I (cTnI) collected
within 3.5 h of ischemic symptoms for predicting clinical outcomes
in 770 patients. cTnT (cutoff >0.1 µg/L) and cTnI (cutoff >1.5
µg/L) were concordant (both positive or negative) in 90.4% of
patients. Among discordant results, 66 were cTnT positive and cTnI
negative vs 8 who showed the reverse (P <0.001). Five
cTnT-positive and cTnI-negative patients died within 30 days; none who
were cTnT negative and cTnI positive died. cTnT showed a slightly
greater association (
2 = 18.0, P
<0.001) with 30-day mortality than cTnI (
2 =
12.5, P = 0.002). The area of the ROC curve for
predicting 30-day mortality was significantly larger
(Z = 2.08; P = 0.0375) for cTnT, at
0.68 [95% confidence interval (CI) 0.600.75], compared with cTnI,
at 0.64 (95% CI 0.560.72). When cTnI and the electrocardiogram (ECG)
were put in a logistic multiple regression model, cTnT added
significant information (
2 = 8.03,
P = 0.045); however, cTnI did not add to a model
containing cTnT and the ECG (
2 = 0.84,
P = 0.657). cTnT provided more information than cTnI
for predicting 30-day mortality early after presentation with acute
coronary syndromes.
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