Viewing Study NCT02886273



Ignite Creation Date: 2024-05-06 @ 9:01 AM
Last Modification Date: 2024-10-26 @ 12:09 PM
Study NCT ID: NCT02886273
Status: UNKNOWN
Last Update Posted: 2021-08-11
First Post: 2016-08-23

Brief Title: DIagnostics Fatty Acids and Vitamin D in SCA
Sponsor: Helse Stavanger HF
Organization: Helse Stavanger HF

Study Overview

Official Title: DIagnostics RBC Levels of n-3 Fatty Acids and Serum Vitamin D in Patients With Out-of-Hospital Cardiac Arrest OHCA
Status: UNKNOWN
Status Verified Date: 2021-01
Last Known Status: ACTIVE_NOT_RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: DIFAD-SCA
Brief Summary: Sudden cardiac death SCD is a major cause of mortality in industrialized countries and represents a major health issue The survival rate after out-of-hospital cardiac arrest OHCA is only 10-15 regardless of first recorded rhythm Prior heart disease is a major risk factor for sudden cardiac arrest SCA and coronary artery disease CAD is the most common underlying cause A better understanding of pathophysiological mechanisms occurring during cardiac arrest CA earlier diagnosis of underlying cause as well as identification of risk factors related to CA may improve patient treatment and increase survival In our out-of-hospital cardiac arrest OHCA-study we intend to investigate whether biomarkers such as copeptin hs-cTnT and NT-proBNP in addition to clinical evaluation may improve risk stratification and supply information related to pathophysiology

Furthermore we intend to gather additional pathophysiological information related to coagulation activation in CA and cardiopulmonary resuscitation CPR as intravascular thrombosis may impair microcirculation and reduce end-organ blood flow which is associated with a poor prognosis We intend to study coagulation activation during and immediately after SCA with regard to outcome and assess the contribution of the intrinsic system measured together with that of the extrinsic system

Low levels of n-3 fatty acids FA are reported as a risk factor for SCD Red blood cell eicosapentaenoic acid EPA docosahexaenoic acid DHA may serve as a useful surrogate of cardiac omega-3 fatty acid status The exact mechanism by which FAs might protect against serious cardiac arrhythmias is not known but they are expected to exert a membrane stabilizing effect during an ischemic episode In our study we intend to evaluate the association between ventricular fibrillation VF and the content of EPA and DHA in red blood cells Furthermore as vitamin D is associated with n-3 FAs in the diet we also aim at investigating the association between 25-hydroxy OH-vitamin D and VF
Detailed Description: Background

Sudden cardiac death SCD also termed sudden cardiac arrest SCA accounts for approximately 15 percent of the total mortality in industrialized countries In Europe the incidence of out-of-hospital Emergency Medical Services EMS attended sudden cardiac arrest SCA is estimated to 816100 000 person-years 525 of which is presumed to have a cardiac cause 1 Coronary artery disease CAD is the most common underlying heart disease associated with out-of-hospital cardiac arrest OHCA 2 SCD is the initial presentation of CAD in 15 percent of CAD-patients 3 Furthermore it is also the most frequent mechanism of death in patients with known CAD accounting for 40-50 percent of CAD-mortality 4 Compared to healthy subjects the incidence of SCD is six- to tenfold higher in the presence of clinically recognized heart disease 5 and cardiomyopathies represents the second largest cause of SCD 6 Despite early advanced cardiopulmonary resuscitation CPR provided by the EMS the mortality rate remains high 1 Due to the dramatic consequence of SCA understanding of pathophysiological mechanisms and early identification of etiology is essential to improve outcome

SCA due to VF may be the presenting symptom of acute myocardial ischemia or may be a consequence of scarring due to a previous myocardial infarction MI Cardiac troponin c-Tn is the most commonly used biomarker for diagnosing an acute myocardial infarction AMI 7 Although earlier detection of AMI may be obtained by the introduction of high sensitivity hs-cTn assays there still remains a troponin-blind period very early after symptom onset 8 9 with the need for serial blood sampling to diagnose or exclude an AMI 7 9 Furthermore there are challenges related to the specificity of elevated levels of hs-cTn 10 11 Therefore measurement of hs-cTn in a single blood draw in the ambulance or at admission may not provide sufficient information for the diagnosis of AMI among patients with OHCA

Lately several studies have demonstrated an incremental diagnostic value of copeptin when added to conventional cTn or hs-cTn for early detection of AMI 12 13 Copeptin levels peak early 0-1 h after symptom onset and are already increased at the time of first medical contact in the ambulance for patients with MI 8 Copeptin used in combination with hs-cTn may therefore improve the diagnosis of AMI in very early presenters and help differentiating the underlying cause of SCD

Copeptin has also been demonstrated to be an independent predictor of adverse events following MI 14 and is shown to be associated with outcome after OHCA 15 16 Less is known about the prognostic value of troponins in patients experiencing a cardiac arrest CA Higher values of hs-cTnT are seen in one-year non-survivors as compared to survivors of OHCA although not shown to be an independent predictor of 12-months survival 10 In our study the objective will be to evaluate the diagnostic and prognostic utility of hs-cTnT and copeptin in SCA patients

Patients with heart failure are at increased risk for ventricular arrhythmias and SCD B-type natriuretic peptide BNP and N-terminal proBNP NT-proBNP have been demonstrated to be useful diagnostic tools to rule out both chronic and acute heart failure 17 Little is known about the natural course of natriuretic peptides during a SCA event but BNP is demonstrated to be an independent predictor of long-term mortality 18 as well as survival to hospital discharge after OHCA of cardiac origin 19 There is also a well-documented association between BNP or NT-proBNP and the short- and long-term risk of death in patients with acute coronary syndrome ACS 20 21 In our study we intend to investigate the diagnostic and prognostic utility of NT-proBNP sampled during or immediately after OHCA

The overall survival rate after OHCA is low Even in successfully resuscitated patients admitted to the intensive care unit ICU the prognosis remains poor Former studies have shown a marked activation of blood coagulation with a concomitant inadequate activation of the endogenous fibrinolytic system in resuscitated OHCA-patients 22-25 Intravascular clotting and no reflow in the microvasculature represent a barrier to successful end-organ perfusion and may influence the outcome in cardiac arrest CA patients 26 Understanding the pathophysiological mechanisms of CA is important to guide management and improve outcome Plasma thrombin-antithrombin TAT complexes fibrin monomers FM and D-dimer are used as specific markers of activated blood coagulation Previous studies have shown markedly increased TAT-levels in patients with nontraumatic OHCA 22 23 Admission TAT is also shown to be a useful prognostic marker in resuscitated OHCA patients and is independently associated with survival after resuscitation from CA 24 D-dimer levels are found to increase after CA and CPR 22 27 Accordingly Adrie et al 28 demonstrated high admission levels of D-dimer in all OHCA patients Furthermore Szymanski et al 29 reported higher D-dimer concentrations on admission to be a strong and independent predictor of mortality in OHCA patients In our study we intend to study the activation of blood coagulation including both the extrinsic- and the intrinsic coagulation pathways during and immediately after SCA with regard to outcome

Most interventions to date do not directly affect the transient pathophysiologic event initializing potentially fatal arrhythmias Instead they attempt to alter and prevent underlying disease like CAD Animal studies have shown that fish oils are protective against ischemia-induced VF 30 Support for these data comes from the Physicians Health Study 31 which is a prospective study of 20 551 men aged 40 to 84 free of cardiovascular disease at baseline with a follow-up period of 11 years As compared to consumption of fish less than once a month fish intake at least once per week was associated with a reduced risk of SCD RR 048 In the same study there was no reduction in the risk of total myocardial infarction non-sudden cardiac death or total cardiovascular mortality and the protective effect of fish was suggested to be due to a reduction in fatal ventricular arrhythmias It has been hypothesized that the lower risk of SCD with higher fish intake may be related to the long-chain n-3 polyunsaturated fatty acids PUFAs EPA and DHA found in fish Consistent with this hypothesis are the observations from the physicians Health Study 31 that the risk of SCD was significantly lower in subjects with blood n-3 FA levels in the highest as compared to the lowest quartile The same potential effect of fish oils to protect against SCD was illustrated in the randomized open-controlled GISSI-prevention study 32 Patients with a recent myocardial infarction receiving n-3 FAs supplements had a significant lower incidence in the combined endpoint of death plus nonfatal infarction and nonfatal stroke at 42 months 126 versus 139 After adjustment for risk factors all of the observed benefit was due to a 20 reduction in the risk of death mostly due to reduction in SCD However a study of 200 patients secured with an ICD implantable cardioverter defibrillator following an episode of ventricular tachycardia VT or VF has not shown a reduction in the recurrence of these arrhythmias after supplementation with EPADHA In that study there was actually a trend toward a higher incidence of VTVF in patients randomized to EPA DHA substitution 33 In that setting the underlying mechanism for the generation of VF might however not be ischemic

The exact mechanism by which FAs might protect against serious cardiac arrhythmias is not known They are important constituents of cell membranes and may affect several electrophysiologic properties such as resting potential action potential repolarization and refractory period Alterations in cellular calcium concentration can contribute significantly to changes in both impulse generation and impulse conduction in myocardial cells Incorporation of n-3 fatty acids in the cellular membrane is shown to affect membrane fluidity which in turn may have an influence on calcium entry or removal An alternative mechanism may be changes effected by n-3 FAs on myocardial production of eicosanoids In particular the inhibition of thromboxane A2 TXA2 production is likely to be of significant pathophysiological benefit since TXA2 is shown to be implicated in myocardial ischemia and arrhythmogenesis 34

A recent study by William S Harris et al 35 has shown that levels of EPA DHA in cell membranes of red blood cells RBC EPA DHA highly correlate with the cardiac EPA DHA level The RBC response to supplementation was also very similar to that observed in the heart Therefore RBC EPA DHA may serve as a useful surrogate of cardiac omega-3 fatty acid status The investigators expect n-3 FAs to exert a membrane stabilizing effect during an ischemic episode and hypothesize that patients suffering VF during the initial phase of their first AMI presentation have lower levels of RBC EPA DHA than matched controls

Over the last years vitamin D is another dietary supplement found to be associated with cardiovascular disease This fat-soluble vitamin primarily derived from sun-exposure and fatty fish has been demonstrated to influence cardiac contractility and myocardial calcium homeostasis 36 and insufficiency of this vitamin may have deleterious effects on cardiac autonomic functions as evaluated by heart rate turbulence and heart rate variability 37 In prospective studies severe vitamin D deficiency has been strongly associated with total mortality cardiovascular events and SCD 38-42 In one study of 3299 patients who were routinely referred to coronary angiography the authors demonstrated hazard ratios for death due to heart failure and for SCD of 284 120-674 and 505 213-1197 respectively when comparing patients with severe vitamin D deficiency 25OHD 25 nmolliter with persons in the optimal range 25OHD 75 nmolliter 43 Demonstrated effects on electrophysiologycontractility and cardiac structure suggest that vitamin D deficiency might actually be a causal factor for development of cardiac diseases The pronounced effect on SCD found in several studies might be an indication of a possible protective effect of high vitamin D-levels against ventricular arrhythmias This is however not well studied and the optimal cut-off-value for protection is not well defined Therefore a comparison of the 25-OH-vitamin D levels between different OHCA categories of patients with and without an acute coronary event may be appropriate

Statistical methods

Statistical analysis will be performed using the statistical package SPSS Statistical Package for the Social Sciences A statistically significant level of p 005 will be applied for all tests

EPA DHA and vitamin D in the different clinical patient categories will be compared to controls collected from the RACS Risk markers in the Acute Coronary Syndromes database NCT00521976

Ethics and confidentiality

The present study is conducted in accordance with the Helsinki Declaration of 1975 and later revisions and accepted by the Regional Board of Research Ethics as well as the Norwegian Health Authorities Analytic data will be related to patient number and not to patient identity According to Norwegian regulations the family of non-survivors will be informed by the attending physician and the inclusion of patients needs to be documented in the hospital records The family of the deceased is entitled to object to the use of any biological samples for research purposes Patients regaining consciousness and mental capability during their hospital stay will be asked personally for a written informed consent For the remaining survivors the next of kin will be asked for permission on behalf of the patient If either the patient or the family refuses participation blood samples already collected at resuscitation and admission will be destroyed

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None