Key result
Cardiac myosin-binding protein C at presentation provided discriminatory power for acute myocardial infarction comparable to high-sensitivity cardiac troponin T.
Why the study?
Does cardiac myosin-binding protein C (cMyC) improve the early diagnosis of acute myocardial infarction compared to cardiac troponins in patients presenting to the emergency department?
Observational (n=1,954)
Yes
Does cardiac myosin-binding protein C (cMyC) improve the early diagnosis of acute myocardial infarction compared to cardiac troponins in patients presenting to the emergency department?
cMyC provides comparable diagnostic accuracy to high-sensitivity troponins for early AMI diagnosis and improves early rule-in/rule-out classification, particularly in patients presenting within 3 hours of symptom onset.
Answers are grounded in this paper and cite their sources.
May enhance early AMI classification over hs-cTnT; hypothesis-generating pending prospective validation.
Background: Cardiac myosin-binding protein C (cMyC) is a cardiac-restricted protein that is more abundant than cardiac troponins (cTn) and is released more rapidly after acute myocardial infarction (AMI). We evaluated cMyC as an adjunct or alternative to cTn in the early diagnosis of AMI. Methods: Unselected patients (N=1954) presenting to the emergency department with symptoms suggestive of AMI, concentrations of cMyC, and high-sensitivity (hs) and standard-sensitivity cTn were measured at presentation. The final diagnosis of AMI was independently adjudicated using all available clinical and biochemical information without knowledge of cMyC. The prognostic end point was long-term mortality. Results: Final diagnosis was AMI in 340 patients (17%). Concentrations of cMyC at presentation were significantly higher in those with versus without AMI (median, 237 ng/L versus 13 ng/L, P <0.001). Discriminatory power for AMI, as quantified by the area under the receiver-operating characteristic curve (AUC), was comparable for cMyC (AUC, 0.924), hs-cTnT (AUC, 0.927), and hs-cTnI (AUC, 0.922) and superior to cTnI measured by a contemporary sensitivity assay (AUC, 0.909). The combination of cMyC with hs-cTnT or standard-sensitivity cTnI (but not hs-cTnI) led to an increase in AUC to 0.931 ( P <0.0001) and 0.926 ( P =0.003), respectively. Use of cMyC more accurately classified patients with a single blood test into rule-out or rule-in categories: Net Reclassification Improvement +0.149 versus hs-cTnT, +0.235 versus hs-cTnI ( P <0.001). In early presenters (chest pain <3 h), the improvement in rule-in/rule-out classification with cMyC was larger compared with hs-cTnT (Net Reclassification Improvement +0.256) and hs-cTnI (Net Reclassification Improvement +0.308; both P <0.001). Comparing the C statistics, cMyC was superior to hs-cTnI and standard sensitivity cTnI ( P <0.05 for both) and similar to hs-cTnT at predicting death at 3 years. Conclusions: cMyC at presentation provides discriminatory power comparable to hs-cTnT and hs-cTnI in the diagnosis of AMI and may perform favorably in patients presenting early after symptom onset. Clinical Trial Registration: URL: https://www.clinicaltrials.gov . Unique identifier: NCT00470587.
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Kaier et al. (2017) conducted an observational in Acute myocardial infarction (n=1,954). Cardiac myosin-binding protein C (cMyC) vs. High-sensitivity cardiac troponin T (hs-cTnT) and I (hs-cTnI) was evaluated on Discriminatory power for acute myocardial infarction (AUC) (AUC 0.924, 95% CI 0.910-0.939, p=0.573). Cardiac myosin-binding protein C at presentation provided discriminatory power for acute myocardial infarction comparable to high-sensitivity cardiac troponin T.
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