Influence of small caliber coronary arteries on the diagnostic accuracy of adenosine stress cardiac magnetic resonance imaging
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- Pilz, G., Heer, T., Graw, M. et al. Clin Res Cardiol (2011) 100: 201. doi:10.1007/s00392-010-0229-4
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Background and aims
Positive predictive value (PPV) of adenosine stress cardiac magnetic resonance (CMR) for coronary artery disease (CAD) is unsatisfactory. We investigated the impact of coronary caliber variability on this limitation in CMR performance.
Methods and results
206 consecutive patients with myocardial ischemia during CMR and subsequent coronary angiography (CA) were studied. Patients were examined in a 1.5-T scanner. After adenosine infusion, myocardial first-pass sequence using gadolinium-based contrast agent was performed and compared with rest perfusion. CAD was invasively confirmed in 165 [true positive (TP); PPV, 80.1%] and ruled out in 41 patients [false positive (FP)]. TP and FP were comparable for pre-test risk and CMR findings. We found a significant association between FP CMR and the presence of a small caliber coronary vessel (proximal diameter < one standard deviation below the mean) supplying the area of ischemia (chi-square 42.6, p < 0.0001). A small caliber artery ipsilateral to the ischemic region was a predictive parameter for FP versus TP discrimination (ROC area, 0.84 ± 0.04 vs. 0.59 ± 0.05; p < 0.0001). Further increment in diagnostic accuracy was achieved by including proximal ipsilateral/contralateral coronary diameter ratios (ROC area, 0.90 ± 0.03; p < 0.03).
Small caliber coronary arteries found as normal variations in right-dominant or left-dominant circulation may account for hypoperfusion in the absence of coronary stenosis and thus may cause FP adenosine stress CMR results. Non-invasive assessment of proximal coronary diameters in the vessel supplying the area of ischemia could reduce FP rates, raise the diagnostic accuracy of CMR for CAD and minimize subsequent superfluous CA.
KeywordsCardiac magnetic resonance imaging Adenosine stress Myocardial perfusion Coronary artery disease Coronary artery caliber
Adenosine-stress cardiac magnetic resonance (CMR) imaging is increasingly proposed for non-invasive assessment of relevant coronary artery disease (CAD). Its high diagnostic sensitivity for the detection of significant CAD has been demonstrated in multiple studies [1, 2, 3, 4, 5]. Likewise, in patients with suspected CAD, normal adenosine stress CMR exams predict an excellent prognosis [6, 7, 8]. In contrast, the overall accuracy of adenosine stress perfusion CMR is presently limited by a lower specificity due to false positive (FP) results [1, 2], and the causes of this limitation are uncertain.
FP myocardial perfusion results have been correlated with variations in coronary anatomy for nuclear medicine single photon emission computed tomography (SPECT) imaging . So far, little is known about the impact of the normal variability of coronary caliber and anatomy on the diagnostic performance of adenosine stress CMR. Aim of our study was to examine whether small caliber coronary arteries found as normal variations in right-dominant or left-dominant circulation may account for visualization of hypoperfusion in the absence of coronary stenosis and thus may result in FP results of CMR in the assessment of CAD.
From 5/2007 to 01/2008 we included 206 consecutive patients with suspected CAD and myocardial ischemia during adenosine-stress CMR (=positive CMR) who subsequently underwent coronary angiography (CA). According to the correlation of CMR and CA, patients were classified as true-positive CMR (TP): positive CMR and relevant CAD in CA or false-positive CMR (FP): positive CMR and no relevant CAD in CA.
Exclusion criteria were a history of myocardial infarction or a visualization of late gadolinium enhancement (LGE) in CMR. All anti-anginal medication and caffeine containing beverages were stopped ≥24 h before the CMR examination. Patients’ pre-test risk was classified according to Morise et al. . The study was carried out in compliance with the Declaration of Helsinki, and written informed consent was obtained from all patients. The protocol of study was approved by the local ethics committee.
CMR studies were performed with a 1.5-T magnetic resonance system (Signa Excite®, GE Medical Systems, Milwaukee, USA) using a 8-element phased array surface coil (cardiac coil, GE Medical Systems). In case of claustrophobia a mild sedation with midazolam was offered. Cardiac function was assessed at rest in three long (two-chamber, three-chamber and four-chamber) and contiguous short axes using steady-state free precession sequences.
After infusion of adenosine at a constant rate of 140 μg/kg per minute over 3 min (Spectris MR injector, Medrad, Indianola, USA), first-pass kinetics of a gadolinium-based contrast agent (Gadodiamide, OmniscanTM, GE Healthcare Buchler, Munich, Germany; 0.1 mmol/kg) was measured during breath-hold in 4–5 contiguous short axis orientations at every heart beat using a hybrid gradient echo/echo-planar pulse sequence (echo time 1.2 ms, flip angle 25°, slice thickness 8 mm, field of view 32–34 × 24–25.5 cm, matrix 128 × 96) as previously described . Ten minutes after stress perfusion a second perfusion study with the same setting was performed at rest. Ten minutes after this second bolus, LGE images were acquired using an inversion-recovery prepared gated fast-gradient echo-pulse sequence (repetition time 6.7 ms; echo time 3.3 ms; flip 20°; inversion time individually adjusted; slice thickness 8 mm; rectangular field of view 30–34 cm; matrix 256 × 160). Again, 3 long and 4–5 short axes as planned in the perfusion study were acquired.
Two experienced investigators evaluated all CMR studies in consensus. Perfusion images were assessed visually. We compared stress to rest perfusion to reduce the potential rate of artefacts . If a deficit was equally present at stress and rest, if it did not follow the subendocardial border, if ghosting artefacts could be seen or if it “blinked” bright and dark it was not regarded as an evident hypoperfusion, but a potential artefact. Such cases were not included into the study. As previously reported , a perfusion deficit was regarded as relevant if affecting >1/3 of myocardial wall thickness in ≥2 neighboring segments (classified according to AHA recommendations ) and persisting >5 heart beats after maximal signal intensity in the cavity of the left ventricle (LV). Patients with a lesser degree of hypoperfusion were not included. The following parameters were measured: LV ejection fraction (%), LV diastolic volume (ml), LV mass (g), LV wall stress (N/m2), transmural extent of ischemia (%), temporal persistence of ischemia (beats). For classification of TP versus FP CMR the area of maximal hypoperfusion was compared for presence or absence of stenosis in CA.
All patients underwent CA within 72 h after CMR examination. Significant CAD was defined as luminal narrowing of ≥70% in CA. Classification of dominance was done using the origin of the posterolateral branch as previously described [9, 13, 14]. If it was dominant and originating from the RCA, we classified the coronary tree as right-dominant, if it was dominant and originating from the LCX, we classified it as left-dominant, and if the coronary trees were equally supplied, we denoted the system balanced. Proximal diameters of LAD, LCX and RCA were assessed by quantitative coronary analysis (QCA). Diameters smaller than one standard deviation (SD) below the mean proximal coronary diameters in our study population were classified as “small caliber”. This analysis was performed by the physician in charge with CA independently of CMR evaluation. Subsequently, ipsilateral/contralateral proximal coronary diameter ratios were calculated (vessel supplying the region of maximal hypoperfusion in CMR divided by the contralateral territory coronary artery diameter: LCX/RCA, LAD/RCA or RCA/LCX, respectively).
Categorical variables are presented as percentage of incidence, continuous variables as mean ± SD. Continuous variables were compared by analysis of variance. Association between groups was assessed by means of chi-square analysis. Relative contribution of the parameters for diagnostic accuracy was calculated by logistic regression analysis and receiver operating characteristic (ROC) curves were generated. Analyses were performed with commercially available statistic software (XLSTAT Version 2008.6.01, AddinsoftTM, Paris, France). For comparison for the areas under the ROC curves (AUC) we used Analyse-it® version 2.11, Analyse-it Software Ltd, Leeds, United Kingdom. A p value <0.05 was considered statistically significant.
Significant CAD was invasively confirmed in 165 (=TP CMR results) out of 206 patients [CMR positive predictive value (PPV), 80.1%] and ruled out in 41 out of 206 patients with previous ischemia in magnetic resonance myocardial perfusion imaging (=FP CMR results). In the 17 FP patients with other stress tests performed prior to CMR, 16 had also shown FP findings indicative of ischemia in these exams: 14 pathological stress electrocardiograms (ECG) and 2 pathological stress echocardiograms.
Baseline patient characteristics
All positive CMR results (n = 206)
FP CMR results (n = 41)
TP CMR results (n = 165)
p value (multivariate)
Age (years), mean ± SD
67.1 ± 9
62.5 ± 11
68.9 ± 8
Morise score (mean ± SD)
15.4 ± 3
15.0 ± 3
15.5 ± 3
Systemic hypertension (%)
Diabetes mellitus (%)
Family history of CAD (%)
Body mass index (kg/m2)
27.2 ± 9
26.8 ± 4
27.3 ± 4
Coronary dominance and coronary artery caliber
Correlation of FP CMR results and coronary caliber
CMR parameters in FP and TP perfusion results
FP CMR results (n = 41)
TP CMR results (n = 165)
LV ejection fraction
65.8% ± 0.03
65.6% ± 0.09
LV enddiastolic volume (ml)
126 ± 27
129 ± 31
LV mass (g)
130 ± 30
137 ± 37
LV wall stress (N/m2)
35.7 ± 5.5
34.7 ± 6.8
Transmural extent of ischemia
41.1% ± 6.8
41.3% ± 7.8
Temporal persistence of ischemia (beats)
8.9 ± 1.1
8.7 ± 1.0
Ischemia in area with small caliber vessel
If adjusted for the disproportion of age and gender by means of matched pair analysis, these results were comparable (ROC curve areas: CMR alone 0.62 ± 0.06; CMR plus coronary caliber, 0.86 ± 0.03; p < 0.001; plus diameter ratio, 0.91 ± 0.04; p < 0.05).
For the 19 FP CMR cases with regular coronary caliber, none of the baseline and CMR parameters shown in Tables 1 and 2 allowed significant discrimination (all p n.s.). The proportion of other pathological previous stress tests was similar in the small caliber (9/22) and regular caliber (7/19) FP CMR subgroup (p = 0.79).
Regardless of a FP or TP result, all patients with ischemia in the area supplied by a small caliber coronary artery were treated conservatively.
Diagnostic performance of stress perfusion CMR for CAD evaluation is presently limited primarily by a lower specificity (FP results). In a large meta-analysis on 24 studies using perfusion CMR imaging mean specificity was 81%. Our study on 206 consecutive patients yielded a PPV of (80.1%), despite adding rest to stress perfusion imaging for recognition of artefacts as proposed by Thomson et al. . Hence our population was representative for current CMR performance.
To the best of our knowledge, the present study is the first to describe an interrelationship between small caliber coronary vessels and CMR visualization of hypoperfusion in the absence of coronary stenosis (FP results regarding CAD). As the main finding of our study, we observed a correlation between FP CMR perfusion results and the presence of a small caliber coronary vessel supplying the area of ischemia in CMR, opposite to the dominant vessel. Of note, in the subgroup of patients with other stress tests performed prior to CMR these exams had similarly yielded pathological findings indicative of ischemia.
Our analysis showed the presence of such a small caliber vessel to be a possible predictive parameter for discrimination of false versus true positive. By adding this information to CMR perfusion, diagnostic performance improved by potentially avoiding up to half of FP CMR results. ROC curve analysis of a combined approach (CMR perfusion and proximal coronary diameter) yielded a significantly better result compared to CMR perfusion alone. This concept is strengthened by the further increment in CMR diagnostic accuracy achieved when additionally including the ratios of ipsilateral/contralateral coronary diameter for FP versus TP discrimination. In contrast, standard CMR function and perfusion criteria were not discriminatory (LV ejection fraction, LV enddiastolic volume, LV mass, LV wall stress, transmural extent of ischemia and temporal persistence of ischemia).
Anatomic studies have shown that while the irrigation of the sternocostal surface of the heart is extremely regular, the inferior or diaphragmatic surface supplied by the circumflex and right coronary arteries is highly variable and gives each heart its own “distinctive physiognomy” . In this respect, the presence of small caliber coronary arteries has been described early. Concerning perfusion physiology, a study in healthy humans found heterogeneity of resting and hyperaemic myocardial blood flow with a broad range of regional distribution .
Although our description of an impact of small caliber coronary arteries for stress perfusion CMR evaluation may be considered disputable, the importance of coronary variability is well known in other cardiovascular imaging conditions. Most recently, Ortiz-Pérez et al.  have shown the impact of variations in coronary anatomy on the assignment of LGE viability assessment by CMR imaging to the specific coronary territory. Their study highlighted that in a per-segment analysis, only 76% of segments followed the distribution of coronary arteries empirically attributed and the discordance reached 67% of cases in a per-patient analysis. In the case of nuclear cardiac imaging, Segall et al.  concluded that the accurate assessment of coronary stenoses by thallium SPECT imaging requires close correlation with arteriography owing to the significant variability in normal coronary anatomy. A main finding of their study was the great variability in blood supply to the inferior and lateral wall, but also in the apex, which is one of the most variable regions with regard to myocardial perfusion . The impact of coronary variability on ECG findings in acute myocardial infarction was first analyzed by Birnbaum et al. Thus, the occlusion in the same site of a coronary artery in different patients may result in a different size and location of the ischemic area at risk and hence the ECG pattern may not be the same in all cases with similar coronary artery occlusion . These findings were confirmed by means of direct CMR scar visualization (LGE) by Rovai et al. .
The coronary distribution and calibers found in our study are in accordance with the literature. Thus, proximal coronary artery calibers measured in our study are in the magnitude of previous studies . Similarly, the higher incidence of right dominant pattern in our study confirms former data .
Given the increasing demand for non-invasive assessment of suspected coronary artery disease , a method with higher sensitivity and specificity compared to the present approaches is strongly needed. A recent study using myocardial perfusion scintigraphy showed that a non-invasive “gatekeeper” approach could make about half of catheterizations redundant . Furthermore, even in high-risk groups substantial savings were possible, and the risk of overlooking patients with severe disease seemed negligible. Besides clinical relevance, the approach of an ischemia-guided selective catheterization has been shown to potentially contribute to saving increasing health expenses , as has been most recently confirmed also for CMR perfusion imaging .
As a valuable alternative to perfusion scintigraphy for non-invasive CAD detection, perfusion stress CMR currently has reached very high sensitivity values, but is still limited by a lack in specificity [1, 2]. Our results suggest that the knowledge of proximal coronary diameter provides added diagnostic value and may increase PPV of perfusion CMR up to 90% without relevant loss of sensitivity. Our data provide preliminary support for an extended CMR algorithm in CAD by adding proximal coronary artery diameter information to the current standard approach of Klem et al. (combination of stress perfusion and LGE ). Applied as a non-invasive gatekeeper, such an extended CMR approach could further reduce FP CMR results, and consequently, the rate of superfluous diagnostic CA. We are aware that the major limitation for implementation of this CMR concept into clinical routine is the fact that magnetic resonance CA (MRCA) to date is still experimental and inferior to coronary computed tomographic angiography (CCTA) [25, 26]. Thus, a most recent attempt to integrate MRCA and CMR perfusion imaging was not successful . Summarized, the usefulness of this extended CMR approach for clinical practice is limited as long as the vessel caliber is not known at the time of CMR. Currently, it is primarily CCTA that could be applied to achieve this goal, particularly if radiation concerns [28, 29] are addressed with development of techniques leading to significant reduction in CCTA radiation exposure [30, 31].
In our study, nearly half of the FP CMR patients showed no association with coronary caliber variations. The reasons for these FP results were not identifiable either by standard CMR parameters, or by knowledge of the proximal diameters. Possible explanations are hypoperfusion due to variations in regional blood flow distribution  or to severe small vessel disease, a known cause of FP CMR results [32, 33]. In addition, the findings might have been caused by unrecognized susceptibility, motion, or ringing artefacts, difficult to distinguish from perfusion deficits despite use of rest perfusion images as in reference . Recent work has shown that one possibility to minimize “dark rim artefacts” was using higher field strength and parallel imaging strategies [34, 35].
The following limitations need to be mentioned for our study. It represents a single center experience with retrospective analysis of prospectively obtained data. Most important, we are aware that the finding of an association between FP CMR results and coronary caliber variations does not prove causal relationship, particularly since we did not perform quantitative perfusion analysis or invasive flow measurements. However, the pathological findings indicative of ischemia encountered in other stress tests support the interpretation of hypoperfusion as a potential cause of the FP results and argue against pure CMR artefacts. Further, we acknowledge that our criterion for classification of a vessel as small caliber may be considered arbitrary. Yet, in the absence of well established definitions the use of the range lesser than one SD below the mean seems plausible. The inclusion criterion of a positive CMR may cause selection bias and thus our results may not reflect the incidence of small caliber coronary arteries in the general population. Finally, since coronary diameter was measured by invasive CA, it remains to be shown whether non-invasive MRCA and CCTA can yield equal results. Thus, our single-center experience should presently be considered as hypothesis-generating result requiring prospective multicenter verification of our findings and evaluation of MRCA’s potential in this concept.
Small caliber coronary arteries found as normal variations in right-dominant or left-dominant circulation may account for visualization of hypoperfusion in the absence of coronary stenosis and thus may cause FP adenosine stress CMR results in the assessment of CAD. Additional non-invasive assessment of the proximal coronary diameter in the vessel supplying the area of ischemia could reduce the rate of FP CMR results and increase PPV for CAD. Our data provide preliminary support for an algorithm which adds information about proximal coronary calibers to stress perfusion CMR imaging to raise the diagnostic accuracy of CMR in the evaluation of CAD and to minimize subsequent superfluous diagnostic CA.
Conflict of interest
The present study was carried out without external funding. G. Pilz discloses consultancy fees and research grants received from GE Healthcare for other clinical studies. The other authors have no competing interests to disclose.
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