Background
Conditions causing chest pain or discomfort, such as an acute coronary syndrome or angina, have a potentially poor prognosis, emphasizing the importance of a prompt and accurate diagnosis [
1]. For patients with acute coronary syndrome (ACS), 12-lead-electrocardiography (ECG), cardiac biomarkers, and echocardiography are used to confirm the diagnosis in combination with the characteristics of chest pain and conventional risk factors [
1,
2]. Echocardiography is a good imaging modality for detecting a new loss of viable myocardium or new regional wall motion abnormality (RWMA) [
1]. However, stable angina cannot be diagnosed or excluded by clinical assessment alone, and non-invasive functional imaging for myocardial ischemia, coronary computed tomography (CT) calcium scanning or angiography, and coronary angiography (CAG) are often needed. Non-invasive functional imaging for myocardial ischemia uses myocardial perfusion scintigraphy with single-photon emission computed tomography (MPS with SPECT), stress echocardiography, first-pass contrast-enhanced magnetic resonance (MR) perfusion or MR imaging for stress-induced wall motion abnormalities [
3]. Using research by Genders et al. [
4], the ESC 2013 guideline contains a similar table of estimated risk percentages to the NICE 2010 guideline. Those with an estimated risk of <15% should be presumed to not have coronary artery disease (CAD). If the estimated risk is >15%, the patient’s left ventricular ejection fraction (LV EF) is a key determinant factor. Therefore, cardiac imaging plays a pivotal role in this type of decision- decision-making through determination of the LV systolic function and subsequent selection of a relevant intervention. However, EF cannot be used as an independent parameter to estimate the probability of the presence of CAD, but it can be used to help choose further studies to detect CAD in combination with clinical assessments. Therefore, routine 2-D echocardiography is less useful in patients with stable angina than in patients with ACS.
An echocardiographic study published in 1972 showed abnormal motion of the LV posterior wall during angina pectoris [
5]. Recently, a non-invasive, load-independent, and reproducible estimator of LV stiffness using 2-dimensional (2D) echocardiography, namely, diastolic wall strain (DWS), has been used to assess wall distensibility in the absence of LV systolic dysfunction [
6]. Decreased DWS is associated with poor prognosis in patients with heart failure with preserved LV ejection fraction (HFpEF) [
7] as well as in those with HF with reduced LVEF (HFrEF) [
8] and is associated with adverse LV remodelling even in patients with normal LV systolic and diastolic function [
9]. Therefore, the aims of this study were to evaluate the relationship between DWS and coronary revascularization as well as to evaluate echocardiographic and other parameters in patients with stable angina who underwent CAG.
Methods
Study design and participants
Of 2375 patients who underwent CAG from January 2013 to December 2015, 440 patients (57% male, average age = 60 years) who were diagnosed with or suspected to have stable angina were studied retrospectively. Patients were referred for evaluation of chest pain or dyspnoea by their general practitioner or by themselves. The character of the chest pain (typical, atypical, or nonanginal) was evaluated, and we excluded any patient with resting pain or suspected unstable angina. A variety of risk factors were recorded during the clinical assessment. Patients who had a prior history of CAD were excluded from this study regardless of their history of coronary stenting. All patients underwent CAG and pre-procedural EF by transthoracic echocardiography (TTE) and were sorted into two groups – the revascularization group (n = 128) and no revascularization group (n = 312). Patients with ACS, chronic kidney diseases, LV EF < 50%, regional wall motion abnormalities, arrhythmia, severe valvular heart diseases, pericardial diseases, thyroid disease, moderate to severe pulmonary hypertension, sepsis, or haemodynamic instability were excluded from this study. We also collected participant data regarding demographic, anthropometric, and laboratory parameters including cardiac biomarkers.
Echocardiography
TTE was performed using standard techniques with a 2.5-MHz transducer. Standard 2-D and Doppler echocardiography was performed using a commercially available echocardiographic machine (Vivid 7R GE Medical System, Horten, Norway) with the same setup interfaced and a 2.5-MHz phased-array probe. With the study participants in the partial left decubitus position and breathing normally, the observer obtained images from the parasternal long and short axes as well as from the apical four chamber and two-chamber and long-axis views. The depth setting was optimized to display the LV on the screen as large as possible and the same field depth was kept for both the four and two-chamber apical views. The sector width was reduced to increase the spatial and temporal resolution. The LV end-diastolic dimensions (LV EDD), end-diastolic interventricular septal thickness (IVSTd), and end-diastolic LV posterior wall thickness (PWTd) were measured at end-diastole according to the standards established by the American Society of Echocardiography [
10]. LV EF was determined by the biplane Simpson’s method. The maximal left atrial (LA) volume was calculated using the Simpson method and indexed to the body surface area. The LV mass was calculated using the Devereux formula: LV mass = 1.04[(LVEDD + IVSTd + PWTd)
3 − (LVEDD)
3] − 13.6. Thereafter, the LV mass index (LVMI) was calculated and indexed to the body surface area. DWS was calculated as [(PWTs) - (PWTd)/(PWTs)] using M-mode echocardiography [
6,
7].
The mitral flow velocities were recorded in the apical four-chamber view. The mitral inflow measurements included the peak early (E) and peak late flow velocities (A) as well as the E/A ratio. The tissue Doppler of the mitral annulus movement was also obtained from the apical four-chamber view. A 1.5-mm sample volume was placed sequentially at the septal annular sites. An analysis was performed for the early diastolic (E’) and late diastolic (A’) peak tissue velocities. As a noninvasive parameter for LV stiffness, the LV filling index (E/E’) was calculated by the ratio of the transmitral flow velocity to the annular velocity. Adequate mitral and tissue Doppler image (TDI) signals were recorded in all patients.
The mean longitudinal global strain (GS) of LV was calculated from the apical 4,3,2-chamber views by speckle-tracking 2D–strain imaging [
11].
Carotid ultrasound
A high-resolution B-mode ultrasound (Vivid 7R GE Medical Systems, Horten, Norway) equipped with a 7.5-MHz linear array transducer was used for carotid ultrasonography. In the longitudinal view, the carotid intima-media thickness (IMT) was determined as the distance from the media adventitia interface to the intima lumen interface on the far wall in a region free of plaque [
12]. The examiner assessed the presence of carotid plaques, which were defined as focal structures that encroached into the lumen by at least 100% of the surrounding IMT value. The common carotid artery IMT (CCA-IMT) was measured between the origin of the carotid bulb and a point 10 mm proximal to the CCA, and the carotid bulb IMT (CB-IMT) was measured in the carotid bulb region. The CCA-IMT and CB-IMT values were determined as the average of the maximum IMT of the left and right CCA and CB.
Statistical analysis
All of the continuous data are expressed as the mean ± SD, and all of the categorical data are presented as percentages or absolute numbers. Continuous variables were analysed using Student’s t-test, and dichotomous variables were analysed using the chi-square test. In addition, multivariate analysis (logistic regression, SPSS for Macintosh, version 10.0.7a, SPSS, Inc., Chicago, Ill., USA) was performed. All variables that had a p value of 0.05 or less were considered statistically significant. The performance of continuous tests was assessed by receiver-operating-characteristic (ROC) curve.
Discussion
The novel finding of this study is that decreased DWS was associated with coronary revascularization in patients with stable angina. The important clinical implication of this finding is that lower DWS may be helpful to predict the need for coronary revascularization in patients with normal pre-procedural LVEF. This suggests a possible role of echocardiography in the diagnosis of stable angina.
Several conditions of either traumatic or atraumatic aetiologies can cause chest pain. To diagnose or exclude ACS, which is a life-threatening condition, prompt evaluation of chest pain using an algorithmic approach is important [
2]. The most common causes of chest pain in outpatients are musculoskeletal and gastrointestinal causes; 10% have stable angina, 5% have respiratory conditions, and approximately 2 to 4% have acute myocardial ischaemia [
14]. The target population of this study was the 10% of patients with stable angina. Among patients with suspected stable angina according clinical, laboratory, and imaging studies, 29% (128/440) of patients needed coronary revascularization (percutaneous intervention: 113; bypass surgery: 14). However, stable angina could not be ruled out in all patients who did not undergo coronary revascularization. CAG was not an absolute indication in at least 312 study subjects. However, sometimes it is not feasible to perform non-invasive functional tests, such as the treadmill test or imaging tests (MPS with SPECT, stress echocardiography or MR perfusion) [
3], in clinical practice. Hence, it is the standard practice at our centre to perform CAG if the suspicion of stable angina is high after clinical, laboratory and imaging studies (chest X-ray, ECG, or echocardiography). If pre-procedural echocardiography in patients with stable angina had some predictable parameters, it would be helpful to determine the patients in whom CAG is indicated. Retrospectively, 312 (71%) of our subjects did not require CAG. Non-invasive imaging plays a multifactorial role in patients with a known or suspected myocardial infarction. In particular, the advantages of echocardiography are to assess the cardiac structure and function and to detect RWMA (myocardial thickness, thickening and motion) [
1]. Echocardiographic contrast agents can improve the visualization of the endocardial border and assess myocardial perfusion [
15]. Tissue Doppler and strain imaging are very helpful tools for the quantification of global and regional function of LV [
11,
15]. However, these modalities have been primarily used in the setting of myocardial infarction. Therefore, we investigated echocardiographic parameters other than LV function or RWMA in the setting of stable angina.
It follows from the concept of the “ischaemic cascade” [
16] that exercise or pharmacologic stress tests (ECG, echocardiography, nuclear test, etc.) are the major tests for evaluating coronary artery stenosis with a high accuracy and prognostic value in patients with clinical suspicion of myocardial ischaemia [
17‐
20]. However, performing these tests before deciding to perform CAG is not always possible in clinical practice due to limitations of time and cost or due to contraindications. Considering the ischaemic cascade (the onset of ischaemia is followed by LV diastolic dysfunction, LV systolic dysfunction, ECG changes and angina, in that order) [
16], we hypothesized that the evaluation of LV diastolic dysfunction might be helpful in patients with suspected stable angina. Fogelman et al. compared multiple posterior wall echograms taken before, during, immediately after, and 5 min after exercise in normal subjects vs. patients with angina; the angina patients showed not only a significantly decreased resting diastolic posterior wall velocity but also a remarkable slowing of the diastolic posterior wall velocity during angina [
5]. DWS, a non-invasive, load-independent, and reproducible estimator of LV stiffness using 2D echocardiography, is used to assess wall distensibility in the absence of LV systolic dysfunction [
6]. Decreased DWS means increased diastolic myocardial stiffness and is associated with poor prognosis in patients with HFpEF [
7] and HFrEF [
8]. Hypertension can cause myocardial fibrosis in association with increased deposition of myocardial collagen, and myocardial fibrosis is responsible for myocardial stiffness. Even in patients with treated hypertension, decreased DWS (cut-off value <0.34) is associated with LV diastolic dysfunction [
21]. The cut-off value of DWS for predicting coronary revascularization in our study was also 0.34 (sensitivity: 89%). Takagi et al. reported that DWS is inversely correlated with post-exercise E/E’ in elderly patients without obvious myocardial ischaemia, and DWS ≤ 0.33 was defined as low DWS [
22]. In addition, low DWS (≤ 0.33) is associated with adverse LV remodelling (higher LV end-systolic volume and increased LV mass index) even in patients with normal LV diastolic function [
9].
Atrial fibrillation (AF), the most common cardiac arrhythmia, is associated with the LV diastolic dysfunction [
23]. Kang et al. observed that diastolic dysfunction (elevated E velocity, E/E’) and dys-synchronous LA were associated with the occurrence of stroke in patients with paroxysmal AF, even in those with a similar CHAD (except prior stroke) score [
24]. Uetake et al. reported that patients with AF had lower DWS than controls (0.35 vs. 0.41) and that decreased DWS (<0.380) was a strong determinant of the prevalence of AF in patients with paroxysmal AF and structurally normal hearts [
25].
Therefore, decreased DWS ≤ 0.33 or 0.34 is definitely associated with increased LV stiffness and diastolic dysfunction in various diseases [
7‐
9,
21,
22,
25] and is associated with poor prognosis in patients with HFpEF, HFrEF [
7,
8] and AF [
25].
Limitations
This study has a few limitations. First, few patients showed elevated pre-procedural cardiac biomarkers. Suspected ACS patients (typical chest pain, RWMA by echocardiography, ST elevation, or significant ST change in association with elevated cardiac biomarkers) were excluded from this study. Only a few patients who were very stable did not have resting chest pain and showed normal LVEF by echocardiography without discernible RWMA were included. Despite the insensitive and subjective nature of the echocardiographic evaluation of RWMA, the patients included in this study were not high-risk patients. Rarely, cardiac troponin can be elevated if the angina episode is prolonged in patients with chronic stable angina [
26]. Second, we evaluated only epicardial coronary obstructions that needed revascularization. Therefore, microvascular angina or coronary spasm was not considered in this study. Third, we did not perform functional studies before CAG in all patients. Finally, the relatively small study population was a major limitation.