Introduction
Acute myocardial infarction (AMI) is defined as a clinical cardiac event that is the consequence of myocardial necrosis caused by ischemia [
1]. Its diagnosis is often based on symptoms, signs, and findings on the electrocardiogram (ECG), but in some patients these findings are non-diagnostic. In these patients, biochemical markers of myocardial necrosis, of which cardiac troponin and creatine kinase isoenzyme (CK-MB) are the preferred biomarkers, play a pivotal role [
2,
3]. A major drawback of these markers is their inability to detect myocardial necrosis in the first hours after symptom onset, since these cardiac biomarkers rise after hours from the onset of myocardial injury. While the outcome of AMI patients has improved considerably [
4,
5], establishing a timely and correct diagnosis remains a challenge in patients presenting early after symptom onset without typical ECG findings.
Recently, the C-terminal portion of provasopressin (copeptin), a marker of acute endogenous stress and cardiovascular hemostasis [
6], has emerged as a promising diagnostic marker for the detection of AMI in addition to conventional cardiac biomarkers of myocardial necrosis in patients presenting early after symptom onset [
7,
8]. In these studies, addition of copeptin to cardiac troponin T (cTnT) improved the diagnostic accuracy of a measurement on admission in patients presenting with chest pain to an emergency department, especially in patients presenting within 3 h after symptom onset. However, although these studies have suggested that copeptin levels are elevated much earlier than CK-MB or cTnT and drop in the 6 h thereafter in patients with AMI, a comparison of temporal release patterns after the onset of AMI between copeptin and conventional cardiac biomarkers has not been made for more than 6 h, when levels were still elevated. We therefore studied the temporal release pattern of copeptin and also studied its relationship with conventional cardiac biomarkers including the newly available high-sensitivity cTnT (hs-cTnT) by frequently sampling patients with ST-elevation AMI within the first 24 h.
Discussion
Although copeptin has been recently described as a potential biomarker for the early detection of AMI, there is little detailed information about its release pattern during the early hours after the onset of AMI. In this study, we demonstrate that in patients with successfully reperfused ST-elevation AMI within 12 h of symptom onset, the release pattern of copeptin is distinctively different from currently available cardiac biomarkers. Copeptin levels peaked within the first hour after symptom onset and fell to normal ranges after 10 h. In contrast, levels of CK-MB, cTnT, and hs-cTnT peaked after more than 14 h and decreased more gradually. Furthermore, a higher copeptin level on admission is related to a shorter time from symptom onset to reperfusion and a lower systolic blood pressure.
Copeptin is derived from the C-terminal portion of the precursor of vasopressin, one of the most important hormones in regulating osmotic and cardiovascular homeostasis and also released in response to acute endogenous stress [
6,
13]. Synthesized in the hypothalamus from the precursor peptide pre-provasopressin, both peptides are released by the neurohypophysis into the circulation. While its exact function is largely unknown, copeptin acts as a stable surrogate marker for vasopressin [
10]. Furthermore, copeptin has been reported as a biomarker in a variety of clinical conditions including sepsis, lower respiratory tract infections, and acute exacerbations of chronic obstructive pulmonary disease [
14‐
19]. The exact trigger for copeptin release in AMI is unknown. Generally considered a marker of acute endogenous stress, copeptin may be released in response to stress occurring with the onset of AMI [
8,
13]. However, copeptin also responds rapidly to changes in fluid status and plasma osmolality [
20,
21]. Our findings, indicating that higher copeptin levels are independently related to a lower systolic blood pressure, are consistent with these reports. Therefore, the quick elevation of copeptin levels in AMI may also be triggered by hemodynamic changes occurring after a drop in blood pressure, or even earlier with elevation of left ventricular end-diastolic pressure after coronary occlusion [
22].
This study confirms and extends the findings of recent previous studies, which reported that copeptin levels in AMI patients were maximal on admission in contrast to cTnT [
7,
8] and dropped to a plateau level after the first day [
23]. The current study, however, is the first to describe the temporal release pattern of copeptin in detail over the first 24 h after symptom onset in AMI and in comparison to the release patterns of CK-MB, cTnT, and hs-cTnT. Copeptin levels in the current study were approximately fourfold higher than in these previous studies, most likely because our population consisted of patients with ST-elevation AMI only instead of a mixed population of AMI with and without ST-elevation. It has been reported that copeptin levels are higher for ST-elevation AMI than for non-ST-elevation AMI [
8].
To date, conventional cardiac biomarkers have limited ability in immediately ruling out AMI in patients presenting early with symptoms that are suggestive for an AMI but with non-diagnostic findings on ECG. The current findings together with the previous studies suggest that copeptin may be a potentially valuable marker on top of cTnT for the detection of AMI. Copeptin levels are not elevated in patients with exercise-induced ischemia [
20] but are significantly higher in patients with a suspected acute coronary syndrome (ACS) presenting to an emergency department in those with a final diagnosis of AMI than in those with a different final diagnosis, including unstable angina and other cardiac and non-cardiac causes of chest pain [
7,
8]. In these patients, adding a copeptin to a cTnT measurement on admission improved the discriminative value compared to a cTnT measurement alone and was of superior value in ruling out AMI. With the combination of copeptin and cTnT, the negative predictive value of a single measurement on admission increased from 88.5 to 95.8% for all AMI suspects and from 82.4 to 92.4% for suspects presenting within 3 h after symptom onset [
8]. The current study illustrates and substantiates these findings, since we confirm that, in patients with an AMI, copeptin is already strongly elevated in the very early phase, while cTnT levels are still low. Because troponin assays lack sensitivity in the early hours after onset of AMI, adding a marker that is sensitive in these early hours and acts independently from cardiomyocyte injury to this conventional biomarker of myocardial necrosis may complement and improve the diagnostic accuracy of a measurement on admission.
Consistent with the other studies [
3,
24], this study indicates that CK-MB and cTnT begin to rise within several hours after the onset of myocardial injury and reach their peak value in the first 24 h. Concordantly, hs-cTnT follows a similar release pattern as cTnT, despite a higher sensitivity and improved precision at the lower limit of detection [
25‐
27]. The only conventional cardiac biomarker that could approach the early presence of marker levels above normal ranges is myoglobin, whose levels begin to rise 1 h after myocardial injury [
3]. Despite its quick release into the circulation, however, myoglobin is not of additional value in a diagnostic strategy including cardiac troponin and is not recommended as a diagnostic biomarker in the routine clinical practice [
28]. Whether copeptin in conjunction with a high-sensitivity troponin assay improves the diagnosis of ACS as suggested [
7,
29] deserves further investigation.
Limitations
Several limitations should be acknowledged as a result of the inclusion and exclusion criteria of the present main study. First, specificity could not be calculated for copeptin and cardiac biomarkers in this study as all patients had a final diagnosis of ST-elevation AMI. Previous studies have indicated that copeptin has a low specificity and is more appropriate as a biomarker to rule out AMI. Second, assessment of copeptin has no value in the clinical practice when ST-elevations are present on the ECG, but it is of potential interest when patients present early and other electrocardiographic and laboratory parameters are yet at normal levels. The temporal release pattern described here is only investigated for ST-elevation AMI and not for non-ST-elevation AMI. In addition, the infarct-related artery was (nearly) completely occluded at presentation in all patients. In a more unselected AMI population with ST-elevation, where a significant proportion of patients present with an open infarct-related artery, it can be speculated that baseline copeptin levels are lower, similar to the lower copeptin levels found in non-ST-elevation AMI [
8], in which the infarct-related artery is usually open. Further studies in AMI patients with and without ST-elevation could clarify whether the lower copeptin levels in non-ST-elevation AMI is the result of patency of the infarct-related artery or of a longer time from symptom onset to admission. Third, primary PCI successfully achieved reperfusion through the infarct-related artery in all patients. Whether the quick normalization of copeptin levels is the mere result of increasing time after onset of AMI or is a specific response to successful primary PCI or other forms of reperfusion requires further investigation. Fourth, the limited number of clinical events in this patient group did not allow us to assess relationships between copeptin levels and the clinical outcome. Copeptin levels on admission have already been reported to be a strong prognostic marker of mortality in cardiovascular patients (with and without heart failure) surviving an AMI [
23,
30,
31]. Fifth, we are unable to explain why BMI is a strong determinant of copeptin levels on admission. While the same is observed for BMI and N-terminal pro-B-type natriuretic peptide [
32], the inverse relation between BMI and biomarkers is poorly understood. Finally, we did not analyze the temporal release pattern of myoglobin as this was not a routine measurement in our center and there was insufficient frozen material stored to allow this additional analysis.
In conclusion, copeptin is elevated in the early hours after the onset of an ST-elevation AMI when other conventional cardiac biomarkers, including CK-MB and cTnT, are still low.
Acknowledgments
The study was funded by the Interuniversity Cardiology Institute of the Netherlands (ICIN). Additional unrestricted grants were received from Janssen-Cilag, Tilburg, the Netherlands, and B.R.A.H.M.S GmbH, Hennigsdorf, Germany. B.R.A.H.M.S GmbH holds patent rights on copeptin. JS is an employee of B.R.A.H.M.S GmbH.