Direct Comparison of Cardiac Myosin-Binding Protein C With Cardiac Troponins for the Early Diagnosis of Acute Myocardial Infarction

被引:87
作者
Kaier, Thomas E. [1 ]
Twerenbold, Raphael [2 ,3 ]
Puelacher, Christian [2 ]
Marjot, Jack [1 ]
Imambaccus, Nazia [1 ]
Boeddinghaus, Jasper [2 ]
Nestelberger, Thomas [2 ]
Badertscher, Patrick [2 ]
Sabti, Zaid [2 ]
Gimenez, Maria Rubini [2 ,3 ]
Wildi, Karin [2 ]
Hillinger, Petra [2 ]
Grimm, Karin [2 ]
Loeffel, Sarah [2 ]
Shrestha, Samyut [2 ]
Widmer, Dayana Flores [2 ]
Cupa, Janosch [2 ]
Kozhuharov, Nikola [2 ]
Miro, Oscar [5 ,6 ]
Javier Martin-Sanchez, F. [6 ,7 ]
Morawiec, Beata [6 ,8 ]
Rentsch, Katharina [9 ]
Lohrmann, Jens [2 ]
Kloos, Wanda [2 ]
Osswald, Stefan [2 ]
Reichlin, Tobias [2 ]
Weber, Ekkehard [4 ,10 ]
Marber, Michael [1 ]
Mueller, Christian [2 ,6 ]
机构
[1] St Thomas Hosp, Kings Coll London BHF Ctr, Rayne Inst, London, England
[2] Univ Basel Hosp, Dept Cardiol & Cardiovasc Res, Inst Basel, Basel, Switzerland
[3] Univ Heart Ctr Hamburg, Dept Gen & Intervent Cardiol, Hamburg, Germany
[4] Hosp del Mar IMIM, Inst Salud Carlos III, Emergency Dept, Ctr Biomed Network Res Rare Dis, Barcelona, Spain
[5] Hosp Clin Barcelona, Emergency Dept, Barcelona, Spain
[6] Hosp Clin San Carlos, Global Res Acute Condit Network, Madrid, Spain
[7] Hosp Clin San Carlos, Emergency Dept, Madrid, Spain
[8] Univ Silesia, Cardiol Dept 2, Katowice, Poland
[9] Univ Basel Hosp, Lab Med, Basel, Switzerland
[10] Martin Luther Univ Halle Wittenberg, Inst Physiol Chem, Halle, Germany
基金
瑞士国家科学基金会; 英国医学研究理事会;
关键词
cardiac myosin-binding protein C; cMyC; myocardial infarction; APACE; troponin I; troponin T; UNIVERSAL DEFINITION; GUIDELINES; ALGORITHM; BIOMARKER; RELEASE; ASSAYS; RULE;
D O I
10.1161/CIRCULATIONAHA.117.028084
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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/ruleout 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.
引用
收藏
页码:1495 / 1508
页数:14
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