http://orcid.org/0000-0001-7419-1899
Correction
6 Mar 2019: The PLOS ONE Staff (2019) Correction: MR findings of microvascular perfusion in infarcted and remote myocardium early after successful primary PCI. PLOS ONE 14(3): e0213636. https://doi.org/10.1371/journal.pone.0213636 View correction
Figures
Abstract
Objectives
The aim of the study was to evaluate CMR myocardial first-pass perfusion in the injured region as well as the non-infarcted area in ST-elevation myocardial infarction (STEMI) patients few days after successful primary percutaneous coronary intervention (PCI).
Materials and methods
220 patients with first time STEMI successfully treated with PCI (with or without postconditioning) were recruited from the Postconditioning in STEMI study. Contrast enhanced CMR was performed at a 1.5 T scanner 2 (1–5) days after PCI. On myocardial first-pass perfusion imaging signal intensity (SI) was measured in the injured area and in the remote myocardium and maximum contrast enhancement index (MCE) was calculated. MCE = (peak SI after contrast—SI at baseline) / SI at baseline x 100.
Results
There were no significant differences in first-pass perfusion between patients treated with standard PCI and patients treated with additional postconditioning. The injured myocardium showed a significantly lower MCE compared to remote myocardium (94 ± 55 vs. 113 ± 49; p < 0.001). When patients were divided into four quartiles of MCE in the injured myocardium (MCE injured myocardium), patients with low MCE injured myocardium had: significantly lower ejection fraction (EF) than patients with high MCE injured myocardium, larger infarct size and area at risk, smaller myocardial salvage and more frequent occurrence of microvascular obstruction on late gadolinium enhancement. MCE in the remote myocardium revealed that patients with larger infarction also had significantly decreased MCE in the non-infarcted, remote area.
Citation: Bethke A, Shanmuganathan L, Shetelig C, Swanson D, Andersen GØ, Eritsland J, et al. (2018) MR findings of microvascular perfusion in infarcted and remote myocardium early after successful primary PCI. PLoS ONE 13(11): e0206723. https://doi.org/10.1371/journal.pone.0206723
Editor: Elisabetta Ricottini, Campus Bio-Medico University of Rome, ITALY
Received: March 20, 2018; Accepted: October 9, 2018; Published: November 9, 2018
Copyright: © 2018 Bethke 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: All relevant data are within the paper and its Supporting Information files.
Funding: The authors received no specific funding for this work.
Competing interests: The authors have declared that no competing interests exist.
Introduction
In patients with acute ST-elevation myocardial infarction (STEMI) the recommended treatment to restore coronary blood flow is percutaneous coronary intervention (PCI) within the first 120 minutes after the STEMI diagnosis has been made [1]. After successful PCI, normal TIMI (Thrombolysis in Myocardial Infarction) flow in the infarct related artery (IRA) post procedure does not always translate into sufficient microcirculation at the myocardial level [2, 3]. Thus, visualization of the patency of the IRA alone is not sufficient for scheduling treatment and physiological aspects are essential. Previous studies have shown that TIMI myocardial perfusion (TMP) may provide additional prognostic information to TIMI flow grade [2, 4, 5].
Cardiac magnetic resonance (CMR) imaging is a sensitive method for evaluation of the microcirculation with high spatial resolution [6, 7]. Over the last two decades CMR imaging has been used in STEMI patients to evaluate treatment and to predict and measure final outcome after the infarction [8–10]. Common CMR parameters reported are left-ventricular end-diastolic volume (EDV), end-systolic volume (ESV) and ejection fraction (EF), infarct size (IS) by late gadolinium enhancement (LGE), microvascular obstruction (MVO), area at risk (AaR) and myocardial salvage [11]. LGE is regarded as the gold standard to predict left ventricular remodeling [12–14] and MVO is associated with the outcome in STEMI patients [15]. First-pass perfusion has been shown to be more sensitive to detect alteration of the microvascular perfusion than early and late gadolinium enhancement [16, 17]. First-pass perfusion is therefore suitable as a supplementary method to LGE and MVO as it might also detect less pronounced microvascular damage missed by other methods [18].
This study included patients from the Postconditioning in STEMI (POSTEMI) study. Compared with conventional primary PCI, PCI combined with ischemic postconditioning did not influence the primary endpoint of infarct size nor the secondary endpoints of MVO, myocardial salvage and ejection fraction, as determined by CMR [19]. The aim of the present study was to evaluate CMR myocardial first-pass perfusion in the injured as well as the non-infarcted area in STEMI patients few days after successful primary PCI.
Material and methods
Study population and treatment protocol
The study population was recruited from the POSTEMI study (ClinicalTrials.gov Po1506) on patients with acute STEMI treated with PCI with or without a postconditioning procedure [20]. The study protocol was approved by the Regional Committee for Medical Research Ethics, South-East Norway and all patients gave written informed consent to participate in the study.
The study protocol is described in detail elsewhere [19, 20]. In brief, patients with acute STEMI with symptoms of less than 6 hours duration and occlusion of a proximal or mid-coronary artery with TIMI flow 0 or 1 before PCI were included in the POSTEMI study. Main exclusion criteria were previous myocardial infarction, occlusion of other coronary arteries than the IRA, ongoing treatment for angina pectoris, thrombolysis given as primary reperfusion treatment, cardiogenic shock, pulmonary congestion, severe hypotension, renal failure (serum creatinine >200 mmol/L) and general contraindication to MRI.
Patients were treated with primary PCI (standard treatment) or primary PCI with postconditioning. The postconditioning was performed with balloon inflations, 4 cycles of 1 min reocclusion and 1 min reperfusion, starting 1 min after opening of the occluded coronary artery [21].
All patients were treated with a stent in the IRA and received a GPIIb/IIIa inhibitor.
Of the 272 patients randomized in the POSTEMI trial, 220 patients were included in the present study (Fig 1). Reasons for not performing an early CMR examination (n = 32) were: not scanner capacity before patient discharge (n = 14); claustrophobia (n = 4); reduced clinical presentation (n = 3); reduced compliance (n = 3); death (n = 2); MRI contraindications (n = 2), high body weight (n = 1) or unknown (n = 3). Of the remaining 240 patients five patients had TIMI flow 0–1 post PCI or non diagnostic first-pass perfusion imaging (n = 15) and were excluded. 220 patients with a CMR examination of diagnostic quality were included in this substudy.
CMR (cardiac MRI), PCI (percutaneous coronary intervention), TIMI (Thrombolysis in Myocardial Infarction).
Clinical follow-up data
Clinical data were collected at one year and a composite endpoint was defined as death, myocardial infarction, unscheduled revascularization >3 months after the index infarction, rehospitalization for heart failure, or stroke.
CMR protocol
CMR was performed within 2 (1–5) days after the STEMI on a 1.5 T scanner (Philips Intera, release 11 or Philips Achieva, release 3.2.1.1; Philips Healthcare, Best, The Netherlands), using five-element synergy-cardiac coil or Sense-cardiac coil, respectively, and vector-based electrocardiography (ECG).
For cine imaging the left ventricle was scanned in two-, three- and four-chamber long axis view using balanced fast-field echo sequences for functional analysis, and short axis images were acquired for complete left ventricular volume analysis. T2-weighted imaging was performed with five short axis slices, covering the ventricle from basis to apex using black blood inversion recovery fast spin echo sequences. The most apical and the most basal slices were rejected and the three mid slices were used for analyses.
First-pass perfusion at rest was performed using ECG triggered fast T1 enhanced gradient-echo technique with segmented K-space and saturation pre-pulse. Three short axis slices were acquired during breath hold, scanning for one minute. The parameters were: TR (time to repeat) 3.2 ms, TE (time to echo) 1.26 ms, flip angle 20° and saturation prepulse delay 200 ms, trigger delay approximately 210 ms, matrix 128 and field of view 350 mm, slice thickness 10 mm, gap 20 mm.
The LGE study was performed 15 minutes after the first-pass study in short axis and two- and four-chamber long axis view, using 3D turbo-field-echo technique with inversion pre-pulses, covering the whole left ventricle. The imaging parameters were: TR 4.5 ms, TE 1.44 ms, flip angle 15° and trigger delay 375–1226 ms, chosen according to the ECG RR interval to fit end-diastole. The optimal T1 for suppression of the myocardium was achieved by the Look-Locker sequence before the diagnostic sequences was performed [22].
In all patients, gadolinium-DTPA (Magnevist, Schering AG, Germany) was injected using Spectris power injector. For the first-pass perfusion imaging, 0.05 mmol/kg body weight was injected at the rate of 3 ml/s into the left brachial vein, followed by 25 ml of saline infused at the same speed [23]. For LGE imaging, an additional dose of 0.1 mmol/kg of Magnevist was injected 15 minutes before acquisition.
CMR analysis
All image analysis was performed offline on a View Forum workstation, Philips Intera extended MR workspace R2.6.3.1. (Philips Medical Systems, The Netherlands). First-pass perfusion imaging was analyzed by one reader (AB) with 5 years experience. All other parameters were analyzed by another reader (PH) with an experience >10 years within the field.
EF was calculated by assessment of the volumes of the endocardial contours in diastole and systole of the short axis images as per standard practice [11].
AaR was assessed in the T2 images as myocardium with a SI of more than 2 standard deviations above the signal intensity (SI) in remote myocardium. The contour of the area with hyperintense signal was than manually drawn in the central 3 of the 5 short axis slices. As the remote area, myocardium supplied by other arteries than the IRA remote to the infarction was chosen. High-grade stenosis in the remote area was ruled out via coronary angiography findings. Myocardial hemorrhage was assessed visually as a hypoenhanced region within the AaR on T2 imagages. The size of the hemorrhage was not assessed.
Myocardial first-pass perfusion was analyzed semi-quantitatively by measuring the SI versus time [11]. SI was measured with manually traced regions of interest in the lumen of the left ventricle, the area of the injured myocardium and in a myocardial area remote to the infarction [6] (Fig 2). The region of the injured myocardium was specified by visual comparison with the LGE study, also including the MVO area. The short axis slice with the greatest infarct extension was considered being the most representative of the infarction. For the lumen of the left ventricle maximum SI was given. The following parameters were calculated for injured and remote myocardium: [24–26]. Time to peak contrast enhancement (TTP) was visually assessed and measured from entry of the contrast medium into the left ventricle to peak myocardial SI [27]. Additionally,
was calculated for each region.
Fig 2A shows perfusion analysis of a patient with an inferior wall infarction with high MCE in the injured and remote myocardium. Fig 2B shows decreased perfusion in the injured myocardium in the inferior wall compared to the remote area. On the LGE study a hypointens area in the endocardium indicates MVO. Green line: ROI blood pool in the left ventricle, blue line: ROI injured myocardium, red line: ROI remote myocardium. Because of the different magnitude of the signal in the blood pool and myocardium a secondary vertical axis has been implemented.
The IS was assessed as a volume in the LGE images by manually drawing the contour of the hyperenhanced area in short axis slices [11]. The volume of the infarction was also related to the total left ventricular myocardial volume and given in percentage. Presence of MVO was defined as a hypointense area in the center of the hyperintense area representing infarcted myocardium, assessed in LGE images. The size of MVO was not measured. Myocardial salvage was defined as [28].
The readers were blinded to treatment strategy and clinical outcome. The intraobserver reliability estimated by the intraclass correlation coefficients for myocardium at risk and infarct size were 0.876, 95% CI (0.628 to 0.963) and 0.985, 95% CI (0.963 to 0.994), respectively [19].
Within observer consistency and agreement was 0.902, 95% CI (0.716–0.972) and 0.906, 95% CI (0.705–0.972) for MCE injured myocardium and 0.878, 95% CI (0.782–0.962) and 0.883, 95% CI (0.774–0.963) for MCE remote myocardium. The Pearson`s correlation coefficient between observers was 0.960, 95% CI (0.903–0.984) for MCE injured myocardium and 0.759, 95% CI (0.488–0.897).
Consistency and agreement between observers was: 0.958, 95% CI (0.919–0.981) and 0.960, 95% CI (0.915–0,980) for MCE injured myocardium and 0.741, 95% CI (0.395–0.981) and 0.741, 95% CI (0.381–0.981) for MCE remote myocardium, respectively.
Design and statistical analysis
This substudy was a cohort study of exposed (standard treatment and postconditioning) versus unexposed (standard treatment) patients.
Peak troponin is given as median (interquartile range) as the distribution was right skewed. Other continuous data were approximately normally distributed and are presented as mean ± standard deviation, binary data as distribution of categories.
To compare patients with different perfusion levels, MCE data of injured myocardium (MCE injured myocardium) were divided into 4 quartiles where quartile 1 represents the highest and quartile 4 the lowest perfusion level. The one-way ANOVA or the chi-square test for categorical variables were used to compare the means of the groups.
Normality and homoscedasticity of the residuals was confirmed for MCE injured myocardium (S1 Fig). Therefore, linear regression analysis was performed for continuous outcomes (dependent variable: EF, ESV, EDV, IS, AaR, myocardial salvage) and logistic regression for binary outcomes (dependent variables: MVO, myocardial hemorrhage). We additionally adjusted for confounding by including age, sex, symptom-to-balloon time, IRA, smoking status, diabetes, treatment for dyslipidemia into all our models. Examination of residual plots of MCE show approximately normally distributed and homoskedastic errors as well as linearity in the explanatory variable, making further variable transformation unnecessary.
Correlation between MCE injured myocardium and the composite endpoint was done with Spearman´s rho.
A p-value <0.05 was considered statistically significant. We used IBM SPSS Statistics 24 for all analysis.
Results
Baseline characteristics of the 220 patients included in this substudy are shown in Table 1. Except for patient age (standard treatment 58.4 ± 10.1; postconditioning 61.6 ±11, p = 0.026) there were no significant differences in baseline parameters, or in CMR parameters, including first-pass perfusion, between the two treatment groups (MCE injured myocardium: standard treatment 92 ± 84; postconditioning 95 ± 74, p = 0.659). Therefore, groups were merged for further analysis.
CMR first-pass perfusion revealed significantly reduced MCE and delayed TTP in the injured myocardium compared to remote myocardium (MCE: 94 ± 55 vs. 113 ± 49, p< 0.001; TTP 15.8 ± 4.9 sec vs. 14.8 ± 4.1 sec, p< 0.001).
When MCE data of the injured myocardium were divided into four quartiles, peak troponin T was higher for patients with lower MCE. However, there were no significant differences in the angiographic data like symptom-to-balloon time, door-to-balloon time, IRA, multi vessel disease, TIMI flow post PCI or the use of thrombectomy related to the level of MCE (Table 2).
Quartile 1 represents the highest MCE and quartile 4 the lowest MCE level.
Comparing the level of MCE to the functional CMR parameters, patients with high MCE injured myocardium (1. quartile) had significantly smaller EDV and ESV and higher EF compared to patients with low MCE injured myocardium (4. quartile) (Table 3). Comparing the level of MCE injured myocardium to the other CMR parameters of infarction, patients with high MCE injured myocardium had smaller IS, smaller AaR and larger myocardial salvage. In patients with high MCE injured myocardium, myocardial hemorrhage and MVO on LGE was significantly less frequent than in patients with low MCE injured myocardium. The differences were significant also when controlled for confounders (age, sex, symptom-to-balloon time, IRA, smoking status, treated dyslipidemia) (Table 4).
Peak SI in the lumen of the left ventricle was not significantly different between the four groups (quartile 1: 2823; quartile 2: 2535; quartile 3: 2524, quartile 4: 2359; p = 0.102).
Analyzes of MCE in the remote myocardium showed that in the 1. quartile MCE in the remote myocardium tended to be lower (not significant) than in the injured myocardium. In all the other quartiles of MCE injured myocardium, MCE remote myocardium was higher than MCE injured myocardium. Data also showed that MCE remote myocardium decreased significantly from the 1. to the 4. quartile (161 ± 47 vs. 76 ± 31, p = < 0.001).
Clinical events were few. Of the 220 patients included in the present substudy 13 patients had a clinical event as defined in the composite endpoint. There was no significant difference between the four groups of MCE injured myocardium (Table 5).
Discussion
In the present study, the results on CMR first-pass perfusion at rest showed no significant differences between patients treated with PCI with or without postconditioning, which is in accordance with the findings in the main study [19, 29].
Normalized flow in the epicardial arteries, in the absence of high-grade stenosis, gives a comparable blood supply to the entire myocardium. Still, microvascular perfusion in the injured myocardium was significantly lower than in the remote area of the left ventricle. The main findings of the present study are, that the level of MCE injured myocardium was associated with EDV, ESV and EF as well as the IS, AaR, myocardial salvage and the occurrence of MVO at LGE imaging. Furthermore, in patients with low perfusion in the injured myocardium also perfusion in the remote myocardium was significantly impaired. Semiquantitative parameters do not depend on the relative difference between injured and remote myocardium and therefore minor changes in remote myocardium can be detected. Recently, research on STEMI patients has focused more on the remote myocardium [30] and parameters evaluating the remote myocardium in an early state after STEMI may be of value when new treatments are tested.
In patients with acute STEMI and restored TIMI 3 flow in the IRA, TMP grade assessed at final angiography has been shown to have prognostic value [2, 4]. The present study focuses on the association between microvascular perfusion assessed with CMR first-pass perfusion and the early outcome in STEMI patients. MVO on CMR is widely regarded as a manifestation of reperfusion injury after STEMI [31, 32]. However, MVO is reported in over 50% of patients post STEMI reperfused by PCI irrespective of post procedural TIMI flow grade [3, 10]. CMR first-pass perfusion is a suitable tool to evaluate microperfusion, as it is more sensitive than MVO on LGE regarding the blood supply to the microvasculature [16, 18].
Despite standardized contrast media dose and infusion rate as well as examination technique and TIMI 3 flow after PCI in the majority of the patients (95.5%), there were significant differences in CMR first-pass perfusion at rest. In the present study, patients with high MCE injured myocardium performed better on functional CMR parameters and presented with significantly smaller IS, and even though they had smaller AaR, they also had higher myocardial salvage. This is in agreement with the findings of Hopp et al. [7], who also found a correlation between peak enhancement in the infarcted myocardium and the presence of MVO at LGE. Ørn et al. also demonstrated larger infarct sizes at six months in the presence of impaired first-pass perfusion [33]. CMR first-pass perfusion might therefore be a more sensitive parameter for evaluation of new treatment strategies [18, 34]. In a recent study Lombardo and coworkers showed a correlation between the extent and transmurality of MVO on first-pass perfusion imaging and left ventricular remodeling [35].
The present study also shows that MCE remote myocardium may be impaired after STEMI treated with PCI. As none of the other CMR parameters in our study, such as T2, LGE or cine sequences showed alterations in the myocardium supplied of other than the target vessel, first-pass perfusion appears to be a more sensitive parameter for evaluating the microvasculature. Also previous CMR studies have found alterations in perfusion of the myocardium adjacent to the infarction and also in the remote myocardium. For instance, Bodi et al. found hypoperfusion in the non-infarcted myocardium in 13% of the myocardial segments adjacent to the infarction [36] and Taylor et al. describes longer TTP in myocardial areas surrounding the infarcted area [37]. Further, Nagao et al. found reduced myocardial perfusion in the remote myocardium in patients with anterior wall infarction [38]. Rogers et al. [39] showed a non-significant improvement of perfusion in the non-infarcted myocardium after myocardial infarction from week one to week seven by 24% in a small study of 17 patients. Stunning might be considered as a possible explanation for these findings [9]. Based on a PET/MRI animal study Lee and colleagues assume a correlation of inflammation in the remote myocardium post STEMI and left ventricular remodeling [40]. Another potential cause could be earlier unnoticed infarction in other vascular territories, although previous infarction and occlusion of a non-infarct related artery was an exclusion criterion in our study. Furthermore, there was no evidence of other infarction on LGE. Non-culprit lesion or collateral flow reduction might cause deprived first-pass perfusion in the remote myocardium [16, 41]. However, coronary stenosis do normally not reduce resting myocardial perfusion [42]. The differences in MCE injured myocardium and MCE remote myocardium were not caused by a more complex coronary disease in patients with lower MCE injured myocardium as the percentage of two- and three-vessel disease was similar between the groups and also TIMI flow post PCI was not significantly different between the groups. As indicated by similar maximum SI in the blood pool in the left ventricle, the differences in MCE between groups were not due to infusion variations or because of individual hemodynamics.
Evolving techniques like T1 mapping have also shown changes in the remote myocardium [30, 43, 44]. Carberry and colleagues demonstrated an association between the extracellular volumes in the remote zone and left ventricular EF [30]. As the changes in ECV in the remote zone were consistent over six months and not accompanied by T2 changes they concluded that underlying replacement fibrosis is a probable explanation. Further, Reinstadler and colleagues found a correlation of native T1 values in the remote zone and major adverse cardiac events [43].
The remote myocardium in patients with STEMI has also been evaluated in a series of studies applying other methods than CMR. In a recent study in patients with acute myocardial infarction, Cheng et al. [45] showed a correlation between impaired coronary flow reserve measured by contrast enhanced echocardiography in the non-infarcted myocardium and left ventricular remodeling and function. Decreased microvascular density and activation of the renin-angiotensin system were proposed as underlying mechanism [45, 46]. Another theory implies that in the situation of an acute infarction the remote myocardium initiates compensatory metabolic reactions [47]. Other studies reveal reduced coronary flow reserve in the infarcted as well as in the remote myocardium in the acute phase of AMI, both with intracoronary measurements [48] and by [15O]H2O positron emission tomography [49]. Impaired vasodilation capacity [47] and dysfunctional autoregulation of the microvasculature caused by neurohumoral activation might in part explain these findings [48].
Echocardiography with circumferential strain could as well show a significant correlation between alterations in the non-infarcted myocardium and diastolic function [50]. It was assumed that compensatory hypercontractility in the remote myocardium in case of STEMI contributes essentially to these findings.
Several histological studies, both in animals and patients found alterations like focal necrosis not only in the infarcted but also in the remote myocardium early after myocardial infarction [51, 52]. Olivetti et al. for instance found apoptosis in 12% of the cardiomyocytes in the AaR and in about 1% in the remote myocardium in a study on patients with large infarctions [53]. These changes in the remote myocardium might contribute to the alterations seen in the present study of CMR first-pass perfusion. However, the data of the present study does not imply a clear explanation and the findings in the remote myocardium remain an observation.
STEMI patients treated with primary PCI do generally have a good prognosis [54, 55]. In our study only 5,9% of the patients had an adverse clinical event within the first year and no significant difference between the MCE groups was found. However, the study was not powered to detect differences in clinical events and one has to be cautious to draw conclusions. As clinical events are rare, reliable surrogate endpoints are needed in studies evaluating treatment regimes in STEMI patients. MCE of the injured and remote myocardium may be used in future trials as a surrogate to reduce sample size.
However, to prevent left ventricular remodeling patients at high risk and in need for intensified therapy need to be identified at an early point in time. The results of the present study indicate that changes in the remote and injured myocardium are related to outcome. As LGE normally does not show alteration in the remote myocardium, we additionally to the standard parameters propose MCE in the injured and remote myocardium as an early marker for risk stratification in STEMI patients treated with primary PCI. However, more standardization of perfusion in the remote myocardium is needed before clinical application. This can be an interesting research area for future investigations.
Limitations
In the present study first-pass perfusion CMR covers only 3 slices and not the entire left ventricle, which can lead to inaccuracy [16]. Great care was taken to standardize contrast infusion, but we cannot completely exclude some variations in infusion and hemodynamics between individual patients.
SI can vary within different distances to the coil. We accounted for that by relating peak SI to baseline SI. Moreover, IRA was evenly distributed between the different groups.
We applied a semiquantitative analysis for the evaluation of first-pass perfusion imaging instead of analyzing the absolute values. However, semiquantitative approaches have been shown to be valuable in STEMI patients [7, 37].
Conclusion
CMR first-pass perfusion can be impaired in both injured and remote myocardium in STEMI patients treated with primary PCI. Impaired first-pass perfusion in the remote myocardium was particularly seen when impairment was larger in the injured myocardium. First-pass perfusion provided additional information to TIMI flow at angiography.
Supporting information
S1 Fig. Residuals plot MCE injured myocardium.
https://doi.org/10.1371/journal.pone.0206723.s001
(TIF)
Acknowledgments
The authors thank the radiographers and staff of the Department of Cardiology and Radiology at the Oslo University Hospital, Ullevål and professor Harald Arnesen for revising the manuscript.
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