http://orcid.org/0000-0003-4321-8977
Figures
Abstract
We aimed to assess the clinical significance of serum levels of neutrophil gelatinase-associated lipocalin (sNGAL) for predicting in-hospital outcomes in patients with ST-elevated myocardial infarction (STEMI). Patients admitted within 24 hours of developing STEMI clinical symptoms were evaluated for sNGAL on hospitalization days 1 and 12. Recurrent myocardial infarction, early post-infarction angina, acute cerebrovascular accident, and death were assessed as adverse outcomes during hospitalization. The actors associated with adverse outcome were evaluated using univariate and multivariate regression analysis. Among the 260 STEMI patients included, 32% had ≥1 adverse in-hospital outcome, and significantly higher sNGAL on day 12, (but not on day 1) compared to sNGAL in patients with favorable outcome (p = 0.033). Type-2 diabetes mellitus, age > 60 years, reduced glomerular filtration rate during hospitalization, and high sNGAL on day 12 were identified as risk factors for adverse in-hospital outcome, associated with a 14% increase for each 1-year increment in age after 60 years, and a dramatic increase (3.2 times) for high sNGAL on day 12, with sNGAL ≥ 1.046 ng/ml indicating complicated hospitalization course. sNGAL concentration on the 12th day was associated with the existing adverse outcomes, acting as a marker of MI severity.
Citation: Karetnikova V, Osokina A, Gruzdeva O, Uchasova E, Zykov M, Kalaeva V, et al. (2017) Serum neutrophil gelatinase-associated lipocalin the estimation of hospital prognosis in patients with ST-elevated myocardial infarction. PLoS ONE 12(7): e0180816. https://doi.org/10.1371/journal.pone.0180816
Editor: Yoshiaki Taniyama, Osaka University Graduate School of Medicine, JAPAN
Received: December 9, 2016; Accepted: June 21, 2017; Published: July 24, 2017
Copyright: © 2017 Karetnikova et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: Due to ethical restrictions imposed by the Local Ethics Committee of the Research Institute for Complex Issues of Cardiovascular Diseases, the data underlying this study are available upon request. To apply for access to these data, interested researchers may contact Dr. Olga Polikutina: Email:ompol@rambler.ru, Phone:+79059002055.
Funding: The authors received no specific funding for this work.
Competing interests: This manuscript has been read and approved by all the authors. This paper is unique and is not under consideration by any other journal and has not been published elsewhere. The authors of this paper report no conflicts of interest. The authors confirm that they have permission to reproduce any copyrighted material.
Abbreviations: MI, myocardial infarction; NGAL, neutrophil gelatinase-associated lipocalin; AKI, acute kidney injury; GFR, glomerular filtration rate; PCI, percutaneous coronary intervention; CABG, coronary artery bypass grafting; CVA, cerebrovascular accident; ACS, acute coronary syndrome; DM, diabetes mellitus; CHF, chronic heart failure; AHF, acute heart failure; CKD, chronic kidney disease
Introduction
Assessing the risk of adverse outcomes in patients with ST-elevated myocardial infarction (STEMI) represents a tasks in modern cardiology, and requires to analyze not only anamnestic data and the characteristics of the index coronary event, but also the records of ongoing or progressing organ failures, which may complicate the course of the disease [1].
STEMI patients are at a particularly high risk of acute kidney injury (AKI) because of the complexity of hemodynamic disorders and adverse effects associated with the use of radiopaque diagnostic and treatment methods [1]. AKI is typically diagnosed based on the assessment of glomerular filtration rate (GFR) and creatinine clearance rate. Nevertheless, in the context of current diagnostic capabilities, biomarkers represent a promising alternative for the diagnosis of myocardial infarction and prediction of its outcomes. Using biomarkers is advantageous because these indicators are universal and allow to estimate early prognosis, as it is possible to assess not only the presence of kidney injury or the severity of comorbid pathologies, but also the risk of cardiovascular events.
Neutrophil gelatinase-associated lipocalin (NGAL) can serve as such a marker, as it is considered one of the most accurate markers acute kidney injury [2]. However, only limited data are available regarding its value in predicting outcomes in STEMI patients. Therefore, the purpose of the present study was to assess the clinical significance of NGAL as a tool for predicting in-hospital outcomes for patients with STEMI.
Materials and methods
Study protocol
This was a retrospective evaluation of patients admitted between 2008 and 2010 to the Kemerovo Cardiology Hospital, in Kemerovo, Russia, with acute coronary syndrome characterized by ST-segment elevation. Data were extracted from the Russian registry of acute coronary syndrome (RECORD) [3].
The study protocol, which received approval from the Ethics Committee of the Research Institute for Complex Issues of Cardiovascular Diseases, was developed in accordance with the Declaration of Helsinki of the World Medical Association (“Ethical Principles for Medical Research Involving Human Subjects”), ammended in 2000, as well as with the “Rules of clinical practice in the Russian Federation”, approved by Order of the Ministry of Health of the Russian Federation (266/19.06.2003). Patient enrollment in the study was voluntary, and each patient provided written informed consent for participation.
Patients
Patients were also included if they had at least two of the following criteria (including elevated biochemical markers of myocardial necrosis): (1) clinical findings of chest pain lasting >20 min; (2) electrocardiographic (ECG) findings with ST-segment elevation on ECG in two or more contiguous leads with the cut-off point of ≥0.1 mV or complete left bundle branch block; and (3) biochemical findings of elevated troponin T levels ≥0.1 ng/ml and/or creatine kinase-MB isoenzyme levels ≥25 IU/l.
The exclusion criteria were: age under 18 years; myocardial infarction requiring complicated percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG); mental illnesses; comorbidities significantly affecting the outcome and prognosis, including cancer, terminal hepatocellular insufficiency, acute infectious diseases, or advanced chronic diseases.
Data collection
The following evaluations were performed for all patients: medical history; physical examination; 16-lead electrocardiography; echocardiography with the assessment of left ventricular ejection fraction (LVEF) and zones of regional contractility violation; blood tests for estimating the levels of troponin T, total creatine phosphokinase and its MB-isohorm, hemoglobin, creatinine, glucose, total cholesterol and lipid spectrum, and serum NGAL (sNGAL). Blood sampling for estimation of sNGAL concentration was collected after radiopaque intervention.
Evaluation of sNGAL (ng/ml) on the 1st and 12th day of hospitalization was performed via an enzyme-linked immunosorbent assay (Hycult Biotech, Uden, The Netherlands), and the results were recorded using a flatbed reader (UNIPLAN; SPC PIKON, Russia). The reference range for sNGAL values was considered at under 0.4 ng/ml.
GFR was estimated using the formula established via the Modification of Diet in Renal Disease study, [4] taking into account the serum creatinine levels, and was recorded from admission until discharge, inclusively (10–14 days). Cases with GFR decline to less than 60 ml/min/1.73 m2 were noted.
The diagnosis of diabetes mellitus (DM) and/or chronic kidney disease (CKD) was extracted from the patients’ medical history records and out-patient medical records, but were also confirmed based on carbohydrate metabolism indicators and creatinine-based GFR recorded during index hospitalization.
For all patients, the modality of reperfusion therapy was established upon admission as follows: PCI in the form of angioplasty and/or stenting of the culprit coronary artery; thrombolytic therapy; or no reperfusion therapy, if common contraindications or technical constraints were present. The time from the onset of chest pain to balloon PCI was 78–11.2 mins.
Totally 109 endpoints were identified: recurrent myocardial infarction– 38 cases, early post-infarction angina– 42, stroke– 4, progressive acute heart failure (increase in Killip class at least by one) was noted in 11cases, mortality– 14; combined endpoints (more than 1 event)– 16.
The following clinical indicators were assessed during hospitalization: manifestations of coronary insufficiency, including development of early post-infarction angina or recurrent myocardial infarction; degree of acute heart failure (AHF), expressed in terms of Killip grade (I–IV); chronic heart failure (CHF) class, according to the New York Heart Association Functional Classification; and in-hospital mortality.
Statistical analyses
Statistical processing of the data was performed using SPSS version 16.0 (SPSS Inc., Chicago, IL, USA). The Pearson criterion (χ2) was used to analyze the differences in frequency. The calculation of odds ratio (OR) with 95% confidence interval (95% CI) was performed using the corresponding option in the program. Two independent groups were compared using the Mann–Whitney U-test. The Kruskal-Wallis test was used to compare several independent groups. To identify the independent predictors of adverse outcomes, the logistic regression method was applied. The differences were considered statistically significant for p-values less than 0.05.
Results
The study included 260 patients (mean age at admission, 57 years; age range, 51–64 years) admitted between January 2008 and December 2010. The baseline characteristics of all patients included in the study are provided in Table 1.
All patients were admitted within 24 hours of the moment of manifestation of clinical symptoms of STEMI. The study included only male patients so as to exclude the potential sex-specific impact on our assessment of STEMI outcomes. DM diagnosis was verified in 23 patients (8.8%), based on medical history data and laboratory parameters (fasting and postprandial glycaemia). The following notable cardiovascular risk factors were found: arterial hypertension (80.7%), overweight status (71.5%), and smoking status (63.0%). Aspirin, β blockers, angiotensin-converting-enzyme inhibitors, and statins were among the most common drugs taken routinely before admission. Myocardial infarction of anterior localization was diagnosed in 47.3% of cases, and the signs of acute heart failure indicated Killip grade I in most patients (86.5%).
The patients were stratified into two groups depending on the occurrence of adverse in-hospital outcomes including recurrent myocardial infarction, early post-infarction angina, acute cerebrovascular accident (CVA), and death. Adverse in-hospital outcome (i.e., the presence of at least one of the above-described outcomes) was noted in 83 patients (32%), who were included in the favorable outcome group. The remaining 177 patients (68%) did not experience in-hospital complications, and were included in the favorable outcome group (Table 2).
In our study, 14 patients (5.1%) died during hospitalization (up to 12 days). The in-patient treatment stage of up to 12 days was completed by 88 patients, but blood sampling was performed in 84 patients at the indicated time, as well as in 172 patients who were hospitalized during this period. Thus, in total, 256 blood samples (93.4%) were analyzed on the 12th day of myocardial infarction. These aspects were clarified in the revised manuscript.
Comparison between the groups indicated that patients older than 60 years prevailed in the group with adverse outcome (47% vs 32.2%, p = 0.002). In the same group, the index myocardial infarction was significantly more likely to be associated with a history of CVA (12% vs 5%, p = 0.044), clinical findings of angina (50.6% vs 36.7%, р = 0.034), and kidney disease diagnosed at the out-patient treatment stage (55.4% vs 38.4%, р = 0.01).
The unfavorable outcome group contained 2.8 times more patients with type 2 DM than did the favorable outcome group (15.6% vs 5.6%; p = 0.008). AHF of Killip grade II-IV class was diagnosed 7 times more often in the unfavorable outcome group (32.5% vs 4.5%; p < 0.05).
In terms of the medication use during hospitalization, we noted more frequent use of diuretics (9.6% vs 5%; p = 0.027), as well as less frequent prescription of statins (43.5% vs 25.3%; p = 0.041) in the unfavorable outcome group; the groups did not differ regarding the in-hospital prescription of other types of medication. The differences in the use of diuretics may be explained by the fact that a greater number of patients with Killip grade II-IV were included in the unfavorable outcome group.
The two groups also differed in terms of clinical and laboratory parameters (Table 3).
Specifically, blood glucose levels on admission appeared to be higher in the unfavorable outcome group (7.8 vs 6.2 mmol/l; p = 0.04). The levels of blood creatinine over the course of hospitalization and at discharge were higher in the unfavorable outcome group (116 vs 105.5 umol/l, with p = 0.009; 99 vs 93 umol/l, with p = 0.023; respectively). A decrease in GFR to under 60 ml/min/1.73m2 during hospitalization was observed 2 times more often in the unfavorable outcome group (8% vs 4.2%; p = 0.0003).
Interestingly, the levels of the kidney injury biomarker sNGAL noted for hospitalization day 1 did not differ between the groups. Nevertheless, sNGAL for hospitalization day 12 appeared to be significantly higher in the unfavorable outcome group (2.1 vs 1.55 ng/ml; p = 0.033; Fig 1).
p—value for differences between groups (p < 0.05).
The correlation analysis suggestedhowed the presence of a direct positive association between sNGAL on hospitalization day 12 and the presence of CKD history, early post-infarction angina, left ventricular systolic dysfunction (LVEF < 40%; Table 4).
Univariate analysis showed that the presence of type 2 DM, age > 60 years, significant GFR decrease during hospitalization, and higher sNGAL on hospitalization day 12 were significant risk factors for the development of adverse outcomes hospitalization (Table 5).
Specifically, GFR decrease during hospitalization, presence of type 2 DM, and significantly higher sNGAL on hospitalization day 12 were associated with a 1.9-, 1.8-, and 10-fold increase in the incidence of adverse outcomes.
By the method of multivariate logistic regression was applied on the set of predictors identified via univariate analysis to have a significant impact on in-hospital outcomes. The predictors were included into the final model in a stepwise manner, and the following effects were noted: an 1-year increment in age in patients over 60 years old increases the risk of adverse outcomes by 14%; higher sNGAL on hospitalization day 12 is associated with a 3.2-fold increase in risk for adverse outcome (Table 5).
The receiver operating characteristic analysis of sNGAL impact on the risk of adverse hospital outcomes revealed an area under the curve of 0.703 (95% CI: 0.43–0.97), suggesting that our risk prediction model has high quality. The threshold for significant risk was found at sNGAL ≥ 1.046 ng/ml, which was associated with a complicated hospitalization course of myocardial infarction.
Discussion
The value of sNGAL as a marker of acute kidney injury is well established, [5] as is its role in the assessment of the severity of kidney injury. Thus, according to some authors, increased levels of this marker can be regarded as one of the indications for hemodialysis [6]. Moreover, the independent association of sNGAL with renal failure and progression of CKD was also noted, which likely underlies the high prognostic value of this marker [7]. The relationship between CKD and cardiovascular diseases is known; specifically, the maximum risk of developing cardiovascular disease, as well as the risk of experiencing an unfavorable course of the ongoing cardiovascular disease have been determined among patients with end-stage renal disease [8]. Furthermore, there is evidence regarding the association between increased sNGAL and total mortality rates in elderly individuals [9].
NGAL is secreted by the epithelium of renal tubules in response to kidney injury, and this process precedes the increase in serum creatinine concentration [8]. On the basis of this feature, NGAL is regarded as a specific and sensitive marker of AKI, in particular after cardiosurgical interventions and administration of radiopaque agents [10]. The prognostic value of sNGAL, previously demonstrated as an accurate marker of kidney damage in terms of unfavorable 30-day prognosis in AHF patients, significantly exceeds that of creatinine; thus, sNGAL may be used as an indicator to complement assessments of the levels of brain natriuretic peptide [11]. The predictive role of NGAL was also shown in patients admitted to the emergency department with AKI, but who did not have any history of kidney disease [12]. However, the role of sNGAL in the prediction of STEMI prognosis remains under discussion. In our present study, sNGAL on hospitalization day 12, but not that on day 1, correlated with in-hospital outcomes; specifically, higher sNGAL on hospitalization day 12 was associated with dramatically increased occurrence of at least one adverse outcome during hospitalization.
Moreover, the unfavorable outcome group contained a greater proportion of patients with significant reduction in GFR over the course of hospitalization, which is consistent with the findings of Bolignano et al. [13]. and suggests that sNGAL may serve as an indicator of residual renal function. According to the “forest fire” theory, the relationship between higher sNGAL and decrease in GFR is related to the fact that NGAL production takes place in viable cells of the inflammatory-modified tubular epithelium, whereas the increase in creatinine concentration and decrease in GFR reflect only the total, irreversible loss of functional nephrons [14]. Viewed from this perspective, sNGAL can be considered to characterize the residual volume of functional nephrons.
In addition, the correlations noted between sNGAL on hospitalization day 12 and other indicators of severe cardiovascular dysfunction including LVEF < 40% and presence of early post-infarction angina, as well as the absence of similar associations concerning sNGAL on hospitalization day 1, highlights the role of sNGAL as a marker of unfavorable course during hospitalization for STEMI. The complications noted during the hospitalization period may represent an independent cause of AKI, and may lead to additional secretion of NGAL.
Conclusions
Using the one-dimensional and multidimensional models, we also demonstrated the value of sNGAL as a factor reflecting the unfavorable course of myocardial infarction. The identified trends suggest that sNGAL can serve as a marker of infarction severity and unfavorable course in the early period of hospitalization for STEMI, and that an increase in sNGAL should be considered a serious development even in patients with absent or minimal clinical manifestations.
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