Oxidized low-density lipoproteins (oxLDL) and oxidized low-density lipoprotein autoantibodies (OLAB) have been detected in human plasma and atherosclerotic lesions. OLAB appear to play a role in the clearance of oxLDL from circulation. Higher levels of OLAB appear to be associated with a reduced risk of a wide range of cardiovascular diseases. We investigated the prognostic value of plasma oxLDL and OLAB in patients undergoing primary coronary balloon angioplasty for acute ST-elevation myocardial infarction (STEMI).
Plasma oxLDL and OLAB concentrations were measured in 56 patients with acute STEMI before primary angioplasty, and then 3 days, 7 days and 1 month after the acute event. Follow-up angiography was repeated 6 months later to detect the presence of restensosis (defined as >50% luminal diameter stenosis). The thrombolysis in myocardial infarction (TIMI) risk score was calculated to determine the relationship between OLAB/oxLDL ratio and TIMI risk scores.
Of the 56 patients, 18 (31%) had angiographic evidence of restenosis. Plasma OLAB concentrations were significantly lower in the restenosis group before angioplasty (181±114 vs. 335±257 U/L, p = 0.003), and at day 3 (155±92 vs. 277±185 U/L, p<0.001) and day 7 (177±110 vs. 352±279 U/L, p<0.001) after the acute event. There was no difference in oxLDL concentration between the two groups. The ratio of OLAB/oxLDL positively correlated with TIMI risk scores before angioplasty (p for trend analysis, p = 0.004), at day 3 (p = 0.008) and day 7 (p<0.001) after STEMI.
Citation: Huang C-H, Chang C-C, Huang C-S, Kuo C-L, Chen C-P, Hsia C-H, et al. (2013) Using Oxidized Low-Density Lipoprotein Autoantibodies to Predict Restenosis after Balloon Angioplasty in Patients with Acute Myocardial Infarction. PLoS ONE 8(10): e74726. https://doi.org/10.1371/journal.pone.0074726
Editor: Ronald J. Korthuis, University of Missouri, United States of America
Received: June 6, 2013; Accepted: August 5, 2013; Published: October 3, 2013
Copyright: © 2013 Huang 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.
Funding: The work was funded by grants 100-CCH-IRP-08 from the Changhua Christian Hospital Research Foundation. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
The main cause of acute myocardial infarction (AMI) is the rupture of vulnerable plaques and the subsequent formation of thrombi . The lipid component of vulnerable plaques is highly enriched with oxidized low-density lipoproteins (oxLDL) , which are released from atherosclerotic plaques into the circulation on rupture . Circulating oxLDL is atherogenic and immunogenic, thereby triggering innate and humoral immune responses . As oxidized low-density lipoprotein autoantibodies (OLAB) play a role in the clearance of oxLDL from the circulation, it has been hypothesized that they may protect against the risk of atherosclerosis . However, whether OLAB is proatherogenic or antiatherogenic has not been established in vivo.
The presence of circulating OLAB may, however, simply reflect the oxidative burden of low-density lipoprotein cholesterol (LDL-C). It is also possible that circulating OLAB might directly or indirectly contribute to atherogenesis . In our previous study of healthy volunteers, we found that a low ratio of serum OLAB to oxLDL concentration was associated with thickening of the intima of the carotid artery and elevated serum LDL concentration. Conversely, subjects with a high OLAB to oxLDL ratio had the lowest carotid artery intimal thickness (CCA-IMT) and lowest LDL levels. These findings suggest that both a high plasma oxLDL and low plasma OLAB contribute to the development of atherosclerosis . Pawlak et al recently found that the ratio of serum OLAB to oxLDL influenced the extent of carotid atherosclerosis and risk of cardiovascular complications in dialyzed patients with renal impairment , leading the authors to hypothesized that the ratio reflects the balance between the modification of LDL induced by oxidative stress and the rate of clearance of oxLDL from the circulation. However, the hypothesis remains to be explored.
In this study, therefore, we hypothesized that the ratio of circulating OLAB to oxLDL (OLAB/oxLDL ratio) concentration may be associated with an atheroprotective phenotype and that thrombolysis in myocardial infarction (TIMI) risk score, a well-known prognostic marker , , may be associated with the OLAB/oxLDL ratio. Certain promising biomarkers have been shown to provide prognostic information about restenosis in patients undergoing balloon angioplasty for AMI . The use of biomarkers in the early detection of patients at high risk of restenosis may be clinically relevant as it may help identify patients who might benefit from targeted pharmaceutical intervention or alternative therapies to reduce restenosis.
Subjects and study protocol
This was a prospective study of 65 consecutive patients with a de novo ST elevation AMI who underwent primary percutaneous coronary intervention (PCI) and thromboaspiration between May 2009 and May 2010. Nine patients who underwent direct stenting were excluded, but the other 56, who underwent a balloon angioplasty, were enrolled into the study. During the study period, guidelines stated that the primary aim of PCI was to achieve revascularization without direct stenting . Venous blood was obtained prior to PCI and at day 3, day 7 and 1 month after the acute event. Blood sampling was undertaken after an 8-hour fast, with the exception of the sample taken prior to PCI. Diagnosis of STEMI was primarily based on the Joint Taskforce universal definition of myocardial infarction . The diagnostic criteria used were: ST segment elevation of >0.2 mV in two or more contiguous electrocardiography (ECG) leads and an increase in cardiac biomarkers (for example troponin I and creatinine kinase (CK) MB fraction) with at least one value above the 99th percentile of the upper reference limit within 24 hours of the onset of pain. The culprit vessel was identified based on clinical, ECG and angiographic findings. All patients were placed on aspirin and clopidogrel prior to PCI, which is the standard regimen in Taiwan. Angiography was repeated for patients who developed angina within 6 months, or after 6 months in asymptomatic patients. The TIMI risk score was calculated for all patients. It was calculated as the weighted sum of several clinical predictors including age ≥75 years (3 points); age 65 to 74 (2 points); history of angina, diabetes, or hypertension (1 point); Killip class II to IV (2 points); heart rate >100 beat/min at the time of presentation (2 points); systolic blood pressure <100 mm Hg at the time of presentation (3 points); anterior myocardial infarction or left bundle branch block (1 point); time to treatment >4 hours from symptom onset (1 point); and weight <67 kg (1 point) . Data obtained from the AMI group included age, sex and the presence of risk factors (for example cigarette smoking, diabetes mellitus, hypertension and hypercholesterolemia), clinical variables and medication history. Smoking index was defined as the number of packs smoked per day × years smoked. The protocol was approved by the Institutional Review Board of the Changhua Christian Hospital, Taiwan, and all subjects gave written and informed consent to participate.
Measurement of plasma biochemical parameters
The plasma oxLDL concentration was determined by a competitive enzyme-linked immune-absorbent assay (ELISA)  with a specific murine monoclonal antibody, mAb-4E6 (Mercodia, Sylveniusgatan, Sweden). The plasma OLAB concentration was measured using a specific ELISA kit (Biomedica, Wein, Austria). The assay was performed according to the manufacturers' instructions.
Plasma total cholesterol, high-density lipoprotein cholesterol (HDL-C), and triglyceride levels were determined using an enzymatic technique as previously described . LDL-C concentration was calculated according to the formula developed by Friedewald et al. , which is as follows: LDL-C = (total cholesterol – high-density lipoprotein-C-triglyceride)/5.
Quantitative coronary angiographic measurements were made by a cardiologist blinded to the patients' OLAB/oxLDL status. Restenosis was defined as a >50% diameter stenosis on a repeat angiography at or within 6 months of the acute event. The TIMI flow  and myocardial blush  grades for assessing microvascular perfusion were also reviewed by the same cardiologist. Characteristic coronary lesions were classified according to the American College of Cardiologists/American Heart Association classification .
Statistical analyses were undertaken using the SPSS statistical software package (SPSS v15.0; Chicago, IL, USA). All parameters are presented as the mean with the standard deviation. Statistical differences between the subgroups with and without restenosis within the AMI group were evaluated using the Mann-Whitney U test. A p value <0.05 was considered statistically significant. A Spearman's rho correlation was used to analyze the relationships between OLAB and patient characteristics. Receiver operator characteristic (ROC) curves were constructed to assess the predictive accuracy of OLAB for restenosis. The areas under the curves (AUC) for predicting restenosis with OLAB were calculated. A general linear model technique was used to evaluate independent associations between OLAB and other measured variables. The Jonckheere-Terpstra test was used to analyze the association between the OLAB/oxLDL ratio and TIMI risk scores. The Jonckheere-Terpstra test is similar to the Kruskal–Wallis test but is applied to samples with a priori ordering, e.g., TIMI risk scores. When there is an a priori ordering, the Jonckheere test has more statistical power than the Kruskal–Wallis test. Since our study was a pilot study, there was no reference data for OLAB in AMI patients. Therefore, it was difficult to estimate sample size and study power.
Baseline clinical characteristics, biochemical data, medication history, and angiographic characteristics of patients with AMI
The AMI group was divided into two subgroups based on the presence or absence of restenosis (a ‘No-Restenosis’ group and ‘Restenosis’ group) in the 6 months after the acute event. Restenosis was evident on angiography in 18 patients (31%). Their baseline characteristics are summarized in Table 1. Serum OLAB concentration was significantly lower in the Restenosis group than in the Non-Restenosis group. There were no significant differences in the cardiac muscle enzyme level, lipid profile, location of the infarct-related artery, ECG findings, lesion characteristics, or quality of initial reperfusion.
Serial circulating oxLDL levels in patients with and without restenosis
There were no significant differences in oxLDL levels before PCI (66±20 mg/dL vs. 68±22 mg/dL, p = 0.716), on day 3 (60±7 mg/dL vs. 65±19 mg/dL, p = 0.326), day 7 (50±12 mg/dL vs. 54±16 mg/dL, p = 0.348), or 1 month (55±23 mg/dL vs. 60±30 mg/dL, p = 0.541) after the acute event (Figure 1).
Serial circulating OLAB levels in patients with and without restenosis
Compared with patients without restenosis, OLAB levels were significantly lower in those who developed restenosis, before PCI (181±114 U/L vs. 335±257 U/L, p = 0.003), on day 3 (155±92 U/L vs. 277±185 U/L, p<0.001), day 7 (177±110 U/L vs. 352±279 U/L, p<0.001), and at 1 month (266±245 U/L vs. 339±340 U/L, p = 0.416) after the acute event (Figure 2).
Serial ratios of OLAB/oxLDL in patients with and without restenosis
Compared with patients without restenosis, the ratio of OLAB to oxLDL was significantly lower in those who developed restenosis before PCI; however, there was no significant difference in ratio between the groups 3 days, 7 days or 1 month after the acute event (Table 2).
Prognostic value of serial OLAB levels in AMI patients after primary balloon angioplasty
The areas under the curves (AUC) for OLAB as a predictor of restenosis were 0.697 before PCI (95% CI, 0.557–0.838, p = 0.018), 0.708 on day 3 (95% CI, 0.570–0.845, p = 0.013), and 0.712 on day 7 (95% CI, 0.576–0.848, p = 0.011) (Figure 3).
The relationship between TIMI risk score and the OLAB/oxLDL ratio
Trends analysis showed that the ratio of OLAB to oxLDL was positively correlated with the TIMI risk score in the subacute stages, namely at baseline, at 3 days and 7 days after the acute event (p = 0.004, p = 0.008 and p<0.001, respectively); however, this relationship was no longer evident 1 month after the acute event of STEMI (Table 3).
Factors correlating with OLAB
The serum OLAB concentration negatively correlated with age, body mass index, waist circumference, oxLDL, LDL-C and total cholesterol, and positively correlated with high-density lipoprotein cholesterol (HDL-C) and TIMI risk score (Table 4).
General linear model analysis of factors affecting OLAB
General linear model analysis was performed to examine the factors that are independently associated with OLAB in the AMI group. We found that the TIMI risk score <3 compared to TIMI risk score ≥3 showed a negative correlation with OLAB (p = 0.045) (Table 5).
In spite of the establishment of guidelines for secondary prevention of coronary artery diseases, many patients still develop restenosis after PCI. Therefore, circulating biomarkers that can help predict restenosis-prone conditions are necessary to improve the follow-up and treatment of the patients who have received PCI for coronary artery disease. In this study, we found that higher OLAB to oxLDL ratio was associated with an atheroprotective phenotype in patients who have undergone primary PCI for STEMI. To the best of our knowledge, this is the first study to comprehensively analyze the significance of circulating OLAB and oxLDL in STEMI. We found that OLAB/oxLDL ratio can be used to predict the likelihood of restenosis in patients who received PCI for STEMI.
In a previous study , we found that healthy volunteers with a low OLAB to oxLDL ratio had greater common carotid artery intima-media thickness (CCA-IMT) and higher LDL levels. Conversely, the subjects with a high OLAB to low oxLDL ratio had the smallest CCA-IMT and lowest LDL levels. These findings suggest that a high plasma oxLDL and low plasma OLAB contribute to the development of atherosclerosis. The same hypothesis has also been evaluated in uremic patients. Pawlak and colleagues  found that patients with no history of cardiovascular disease (CVD) undergoing renal dialysis had lower serum oxLDL and higher OLAB concentrations than dialyzed patients with CVD and that CCA-IMT was positively associated with oxLDL/OLAB ratio. Children and young adults, who typically are at very low risk of atherosclerosis, have significantly higher levels of circulating OLAB and very low levels of oxLDL compared with healthy older adults , . Shoji et al. have also reported an inverse relationship between circulating oxLDL and OLAB levels in healthy subjects, which is consistent with our findings in our previous study .
OLAB binds oxLDL and, in turn, decreases circulating oxLDL levels . Additionally, OLAB levels appear to be negatively correlated with indices of oxidative stress  and negatively associated with the severity and extent of stenotic coronary lesions . Therefore, OLAB may protect against atherosclerosis by attenuating oxidative stress. We hypothesize that under normal physiological conditions, there is a dynamic balance between circulating oxLDL and OLAB, where OLAB prevents an increase in circulating oxLDL.
This hypothesis is based on the results of several studies. For example, apolipoprotein E (apoE)-deficient mice demonstrate an ectopic overexpression of liver lectin-like oxLDL receptor-1 (LOX-1), which in turn enhances the hepatic uptake of oxLDL . As a result, these animals have decreased levels of plasma oxLDL and show a slower progression of atherosclerosis . These findings clearly demonstrate that a lower level of oxLDL is beneficial in preventing atherosclerosis. Furthermore, it has been reported that treatment with recombinant antibodies against aldehyde-modified apoB-100, a component of oxLDL, reduces plasma levels of oxLDL by 34%, dramatically reduces atherosclerosis, and inhibits restrictive vascular remodeling in mice expressing human apoB-100 . These observations support the notion that OLAB levels not only reflect the extent of atherosclerosis, but also play a role in maintaining lower levels of circulating oxLDL. Our study concurs with the conclusions of Pawlak and colleagues, who proposed that the OLAB to oxLDL ratio should be seen as a new biomarker that reflects the balance between in vivo oxidative stress burden and the clearance rate of oxLDL from the circulation . Based on these findings, it is clear that measuring the levels of either oxLDL or autoantibodies alone is insufficient. Instead, clinicians should assess the reciprocal changes between circulating oxLDL and OLAB levels.
Within this cohort, oxLDL levels was similar between patients who developed restenosis and those who did not, allowing the direct impact of circulating OLAB levels on restenosis following primary balloon angioplasty to be examined without adjusting for oxLDL. We found that the prognostic value of OLAB in predicting restenosis within 7 days after STEMI is better than the OLAB/oxLDL ratio. As shown in Table 2, serial ratio was only significant before PCI. However, the OLAB levels at different time points differed significantly within 7 days after STEMI. We also found that the maximum area under the curves (AUC) for OLAB/oxLDL ratio was 0.682 at 7 days, which was less than the AUC for OLAB (0.712) (data not shown). A larger sample size is needed to determine the best cut-off value of OLAB in predicting restensosis in patients with STEMI who receive primary angioplasty. We found an inverse relationship between the concentration of circulating OLAB and several markers of atherosclerotic risk (i.e. body mass index, waist circumference, oxLDL, LDL, and age), which is in broad agreement with the findings reported by Che and colleagues . Additionally, the serum concentration of OLAB was found to positively correlate with that of HDL-C.
There is also a temporal element to the importance of OLAB. For example, an early decrease in circulating anti-oxLDL antibodies has been shown to be associated with the severity of coronary artery disease after acute coronary syndrome in patients with metabolic syndrome . We found a high concentration of oxLDL immediately after STEMI, which was presumably released into the circulation by plaque rupture and triggering inflammatory and immune responses, which were neutralized by OLAB after 3 days. Although OLAB levels gradually returned to baseline after the acute episode, circulating oxLDL subsequently remained at lower levels. Other treatments may also influence OLAB concentration, such as control of hypertension , and we found no significant difference in OLAB levels between the restenosis and non-restenosis groups after 1 month.
We also found that the ratio of OLAB to oxLDL positively correlated with TIMI risk score at baseline and on days 3 and 7, but not 1 month, after STEMI. The TIMI risk score is a simple and well-validated clinical risk score, which is used to predict 30 days to 5 years mortality after STEMI , . It also may serve as a risk stratification tool to help clinicians choose the most appropriate therapy. Our findings suggest that a higher OLAB/oxLDL ratio might be protective against the adverse sequelae of the acute insult, highlighting the importance of the dynamic balance between oxidative stress burden and oxLDL clearance rate. General linear model analysis indicated that the association between OLAB and TIMI risk score was independent of other factors, including age, sex, and the extent of heart muscle injury and the location of the infarct related coronary artery. Therefore, STEMI patients with a TIMI risk score ≥3 but with a low OLAB/oxLDL ratio should receive aggressive therapeutic intervention to improve clinical outcome. Manipulating the ratio, either by elevating OLAB levels or decreasing oxLDL concentration, may provide a preventive treatment strategy.
The limitations of this study include the relatively small size of the cohort, and the fact that OLAB and oxLDL were only tested within 7 days and 1 month after the acute event. Therefore, studies with larger numbers of participants and blood samples taken 14 days and 21 days after STEMI are needed to further test our hypothesis. We also excluded patients with STEMI who underwent direct stenting; however, this provided us with the chance to study the influence of oxLDL and OLAB levels on restenosis in patients who have not received direct stenting. Further studies are warranted to clarify the molecular mechanisms that underpin the possible protective effects of autoantibodies against restenosis, including in patients receiving coronary stents.
We found that patients with lower OLAB levels within 7 days after STEMI were significantly more likely to have restenosis in the infarct-related artery after primary angioplasty. The ratio of OLAB to oxLDL positively correlated with the TIMI risk score in the subacute stages of STEMI. Our data support the hypothesis that higher circulating OLAB/oxLDL ratio is associated with an atheroprotective phenotype and that it is a potential prognostic biomarker for post-STEMI complications.
Conceived and designed the experiments: C.-H. Huang, C-CC C.-S. Lin C.-S. Liu. Performed the experiments: C-SH C-LK. Analyzed the data: C-PC C.-H. Hsia Y-MC. Contributed reagents/materials/analysis tools: H-TC C-CF L-SL P-TY C-DT. Wrote the paper: C.-H. Huang C-CC.
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