- Open Access
Quantitative analysis of late gadolinium enhancement in hypertrophic cardiomyopathy
© Aquaro et al; licensee BioMed Central Ltd. 2010
- Received: 8 October 2009
- Accepted: 7 April 2010
- Published: 7 April 2010
Cardiovascular Magnetic resonance (CMR) with the late gadolinium enhancement (LGE) technique allows the detection of myocardial fibrosis in Hypertrophic cardiomyopathy (HCM). The aim of this study was to compare different methods of automatic quantification of LGE in HCM patients. Methods: Forty HCM patients (mean age 48 y, 30 males) and 20 normal subjects (mean age 38 y, 16 males) underwent CMR, and we compared 3 methods of quantification of LGE: 1) in the SD2 method a region of interest (ROI) was placed within the normal myocardium and enhanced myocardium was considered as having signal intensity >2 SD above the mean of ROI; 2) in the SD6 method enhanced myocardium was defined with a cut-off of 6 SD above mean of ROI; 3) in the RC method a ROI was placed in the background of image, a Rayleigh curve was created using the SD of that ROI and used as ideal curve of distribution of signal intensity of a perfectly nulled myocardium. The maximal signal intensity found in the Rayleigh curve was used as cut-off for enhanced myocardium. Parametric images depicting non enhanced and enhanced myocardium was created using each method. Three investigators assigned a score to each method by the comparison of the original LGE image to the respective parametric map generated.
Patients with HCM had lower concordance between the measured curve of distribution of signal intensity and the Rayleigh curve than controls (63.7 ± 12.3% vs 92.2 ± 2.3%, p < 0.0001).
A cut off of concordance < 82.9% had a 97.1% sensitivity and 92.3% specificity to distinguish HCM from controls. The RC method had higher score than the other methods. The average extent of enhanced myocardium measured by SD6 and Rayleigh curve method was not significant different but SD6 method showed underestimation of enhancement in 12% and overestimation in 5% of patients with HCM.
Quantification of fibrosis in LGE images with a cut-off derived from the Rayleigh curve is more accurate than using a fixed cut-off.
- Cardiovascular Magnetic Resonance
- Late Gadolinium Enhancement
- Normal Myocardium
- Late Gadolinium Enhancement Image
- Remote Myocardium
Late gadolinium enhancement (LGE) cardiovascular magnetic resonance (CMR) allows detection of myocardial fibrosis in patients with hypertrophic cardiomyopathy (HCM) . Previous studies showed the presence of LGE in approximately 75-80% of patients with HCM [2, 3]. Quantification of LGE can be relevant for clinical purpose if we consider that myocardial fibrosis has been postulated to be an important arrhythmogenic substrate of HCM [4, 5]. The association between the extent of delayed enhancement and the number of risk factor for arrhythmic event was demonstrated in younger patients. However, quantification and characterization of LGE in HCM patients is difficult because of the intramyocardial patchy distribution of LGE and the presence of myocardial areas mildly enhanced, that may represent a sign of initial, non confluent, myocardial fibrosis at interstitial level (plexiform fibrosis). Plexiform fibrosis has been shown to be more evident in patients with higher arrhythmic risk . Several methods assessing the extent of LGE have been proposed. In the qualitative methods the number of myocardial segments involved are visually assessed [8, 9]; in semiquantitative methods an operator manually traces the contours of the enhanced area. These methods are strictly operator-dependent causing unavoidable intra- inter-observer variability. The most used quantitative method is characterised by placing a region of interest (ROI) in the normal myocardium and using a cut-off for delayed enhancement of mean intensity plus 2 standard deviations . Recently mean of remote myocardium plus 6 standard deviations was used as cut-off . However these methods have many limitations: the site of ROI, the assumption of a Gaussian distribution of the signal intensity in the nulled myocardium, the fixed cut-off value for identifying enhanced areas. We proposed a new method of quantification of LGE in patients with HCM without these limitations. Therefore, aim of this study was to compare methods of quantification of LGE in patients with HCM.
Forty consecutive patients (30 male, mean age 40 ± 14 year) with a known diagnosis of HCM entered the study. Diagnosis of HCM was based on previous described criteria . Twenty healthy normal subjects (16 males, mean age 38 ± 10 years) were enrolled as control group. As inclusion criteria controls had not familiar history of HCM or sudden cardiac death. The study was approved by the internal Ethical Committee of Clinical Physiology Institute.
Cardiovascular Magnetic Resonance
CMR was performed using a 1.5T whole body scanner (CVi, HD release, GE Healthcare, Milwaukee, USA). An 8-element (4 anterior and 4 posterior) cardiac phased-array receiver surface coil was utilized for signal reception. Functional parameters of the left ventricle were obtained by acquiring cine short axis images from mitral valve plane to the apex with a steady-state free precession (FIESTA) pulse sequence with the following parameters: 400 mm field of view, 8 mm slice thickness, no gap, 1 NEX, 12 views per segment, TE/TR 1.6/3.2, flip angle 45°, matrix 224 × 192, and reconstruction matrix 256 × 256. End-diastolic wall thickness was measured in all the myocardial wall segment in order to confirm the diagnosis of HCM. LGE images were obtained by an Inversion Recovery Gradient Echo pulse sequence with an inversion time optimized to null signal from normal myocardium. Images were acquired 10 minutes after contrast medium (Gadolinium-DTPA, 0.2 mmol/kg) in the short axis views from the mitral valve plane to the ventricular apex. The following parameters were used: field of view 400 mm, slice thickness 8 mm, no gap between each slice, repetition time 4.6 msec, echo time 1.3, flip angle 20, field of view 360 mm, acquisition matrix 224 × 192, reconstruction matrix 256 × 256. The inversion time was optimized in order to nullify the signal from normal myocardium (range 240-300 msec).
Myocardium signal model
where m represents the measured signal, K the number of phased array coils, and the unit step function ε (m) is used to indicate that the expression is valid only for nonnegative m values. σ is the standard deviation of noise that can be estimated from image background.
A normalized histogram of the signal intensities in ROIs was evaluated for each normal subject and HCM patient. A curve of the distribution of pixel intensity in the whole myocardium was obtained. Each curve distribution was normalized respect to the total number of pixel measured and expressed in percentage. Figure 1B shows the measured distribution of the myocardial signal in normal patients as a normalized histogram, obtained by the methodology described in the next paragraph. The best Gaussian fitting obtained by the Levenberg-Marquardt fitting algorithm is showed as well. The measured fitting error is 3.5%. The measured and Gaussian estimate distribution are significantly different (t = 3.943, p < 0.0001).
We compared two approaches to quantify the extent of higher and mild enhancement in patients with HCM. In the first approach (SD2 method), mean SI and SD measured in the myocardial-ROI were used: higher enhancement was defined as myocardium with SI >mean of myocardial-ROI plus 2 SD.
In the second approach (SD6 method), mean SI and SD measured in the myocardial-ROI were used: higher enhancement was defined as myocardium with SI >mean of myocardial-ROI plus 6 SD.
We proposed a method of quantification of LGE using the Rayleigh curve (RC method). Briefly, as evidenced in figure 2A, LGE was defined as myocardium having signal intensity > the maximal signal intensity measurable in the Rayleigh curve (red line).
Using the different thresholds of signal intensity derived from the three methods simplified parametric maps were created from each original LGE image depicting with different colours areas of normal myocardium and enhanced myocardium.
In order to compare the two methods of analysis the parametric map obtained from each methods was compared with the respective original image by three independent expert investigators (GDA, ES, GD) and a score ranging from 1 to 4 (1 = not suitable, 2 = sufficient, 3 = good, 4 = excellent) was given. The mean score for each method was calculated in each patient. If a score of ≥ 3 was not assigned, the investigators specified if an underestimation of overestimation was performed by the methods by the visual comparison of the original image and the respective parametric map. Overestimation was defined when the area of enhanced myocardium (pink region) in the parametric map exceeded the visual appreciation of the enhanced myocardium in the original image. At the opposite, underestimation was defined when the area of enhanced myocardium depicted in the parametric map was smaller than the corresponding area of enhancement in the original image.
The extent of higher enhancement and mild enhancement in percentage respect to the ventricular mass was automatically measured using both the methods of analysis in each patient.
Contrast-to-noise ratio and signal-to-noise ratio were measured in the non-enhanced myocardium in order to evaluate the myocardium nulling. Contrast-to-noise ratio was measured with the formula: 2 × (mean myoI - mean bkI)/(SD myoI + SD bkI), where myoI is the mean signal intensity of an ROI placed in non-enhanced myocardium and bkI is the signal intensity of an ROI placed in the background . By the above formula, in perfectly nulled myocardium Contrast-to-noise ratio should be equal to 1.
All data were analysed with the use of JMP version (4.0). The inter-observer variability for the assigned score was evaluated by the Kappa test. Data are presented as continue variable and proportions (percentages). Continuous variables are expressed as mean ± 1 SD. Two-way analysis of variance (ANOVA) analysis was used to compare tysis. A p value < 0.05 was considered statistically significant. A receiver operating characteristics (ROC) curve was used to evaluate the sensitivity and specificity of the concordance between the measured distribution curve of signal intensity and the Rayleigh curve to differentiate between patients with HCM and the other groups (control group and athletes).
Summary of clinical data for the entire population
40 ± 14
38 ± 10
LV mass index (g/m2)
107 ± 36
64 ± 14
77 ± 17
78 ± 12
Maximal ED thickness (mm)
19 ± 5
9 ± 4
Ejection fraction (%)
68 ± 10
65 ± 8
Method comparison in HCM and controls
p value (vs RC)
3.75 ± 0.4
1.45 ± 0.5
3.12 ± 0.5
Extent of enhancement (% mass)
3.66 ± 5.1
12.2 ± 5.4
5.52 ± 7.2
3.8 ± 0.5
1.05 ± 0.5
3.6 ± 0.5
Extent of enhancement(% mass)
5.4 ± 5.9
SD6 methods committed overestimation in 2 (5%) patients with HCM and in 1(5%) patients in the control group, underestimation in 5 (12.5%) patients with HCM.
RC method did not commit "underestimation" in patients with HCM but showed "overestimation" in 1 patients (5%) in the control group.
As evidenced in table 2, the average extent of enhanced myocardium was significantly higher in SD2 method than the other methods while no significant differences were found between SD6 and RC methods.
In the present study, three different quantitative methods to detect and quantify enhanced myocardium in LGE images in HCM patients have been compared. The results showed significant differences between the methods. This may result from two main factors: 1) the threshold values of SD above the mean signal intensity of the reference ROI; 2) the site of the reference ROI.
The approach of 2 SD and reference ROI within the myocardium (SD2 method) was largely used as semi-quantitative method for quantification of LGE in literature. In our study, this method showed a larger overestimation of the extent of LGE in comparison with the method we proposed, and resulted unsuitable for an operator independent quantification of LGE. As shown in figures 4 and 5, using as threshold 2 SD above the mean intensity a large amount of normal myocardium is considered as pathologic committing a large overestimation, linked to both the reduced number of SD used and to the low value of the SD found in the remote myocardium. In fact, this method does not consider that the distribution of signal intensity is much closer to a Rician distribution rather then to a Gaussian fitting as showed in methods. Similar result were found by Bodarenko et al.. In that study the extent of delayed enhancement in myocardial infarction was measured using different cut-off (from >2 SD to >6 SD above the mean signal intensity) derived from a ROI placed in remote myocardium. Also in myocardial infarction large overestimation of infarct size was found using a cut-off of >2 SD above the mean. Finally, in HCM patients the detection of area of "normal" myocardium can be unsuccessful due to the presence of large amount of plexiform fibrosis. Instead, choosing ROI in the background had several advantages: the ROI size can be bigger increasing the statistic counting; signal artefacts originated by the partial volume effect and unnoticed presence of fibrosis in myocardium are avoided; finally signal intensity distribution in the image background and in perfectly nulled myocardium are exactly the same.
A cut off of >6 SD above the mean of remote ROI was used in previous studies [11, 19] as fixed threshold to quantify enhanced myocardium. In this study this SD6 method had higher mean score than the SD2 method in HCM and control groups. Yet, mean score of SD6 method was not significant different to RC method in control group but it was significant lower in HCM group.
Although the mean extent of enhanced myocardium measured by SD6 method was not significantly different from the extent measured by the RC methods, SD6 committed overestimation of enhanced myocardium in 12% and underestimation in 5% of patients with HCM.
We proposed a more complex method of quantification combining the use of Rayleigh curve and the measured curve of distribution of signal intensity. Rayleigh curve, created using the SD of the background ROI, was considered a model of the ideal distribution of signal intensity in a perfectly nulled myocardium. In fact, when myocardium is perfectly nulled, its signal derives only from the signal noise and it should be absolutely identical to the background signal. Thus, in perfectly nulled myocardium the signal intensity ratio between background and myocardium evaluated by the contrast-to-noise ratio should be equal to 1. It was previously demonstrated that the distribution of noise in of MRI image is Rician and it could be approximated to a Rayleigh curve [13–17]. Because the signal in the nulled myocardium should be only the noise, its curve of distribution of signal intensity should necessarily resemble a Rayleigh curve. Thus, the higher the concordance between the Rayleigh curve calculated from the signal of background and the curve of distribution of myocardial signal intensity, the higher is the probability that the myocardium is normal. Thus an enhanced, probably diseased, myocardium have a curve of signal distribution very different from the Rayleigh curve. In this study patients with HCM had a mean concordance of 64%, whereas controls had a mean concordance of 92% between Rayleigh and distribution of SI curve.
Furthermore, regions of myocardium with signal intensity higher than the maximal value of the Rayleigh curve have very high probability to be enhanced. With this assumption, any signal intensity higher than the maximal signal intensity derived from the Rayleigh curve was considered pathologic (enhanced myocardium). This new method for quantification of enhanced tissue in LGE images had higher average score than the other methods without committing any over- or underestimation in the HCM group.
Results of this study suggest that the measurement of the degree of concordance between the Rayleigh curve and the measured curve of distribution of signal intensity could be a valuable approach to distinguish between HCM and controls.
The higher the involvement of myocardium, the lower the concordance between the ideal and measured curve. A cut off of 82.9% of concordance had higher sensitivity and specificity to distinguish between HCM and controls. This could be potentially useful for the differential diagnosis between HCM and other causes of left ventricular hypertrophy as athletes heart, acromegaly. The value of this parameters in the clinical setting should be evaluated by further studies.
Another advantage of this method respect to the others is the absence of a fixed cut-off. In fact the cut-off derived from the Rayleigh curve is variable and depends from the mean signal intensity and SD of the background-ROI. Thus, when the signal intensity and SD of the background is higher because of a higher signal noise, the generated Rayleigh curve modifies its morphology and the cut-off is shifted to higher value. In this way the risk of under- and overestimation of the enhanced myocardium is minimized. Contrarily, using a fixed cut-off, when the images are noised the detection and the quantification of the enhancement myocardium could be underestimated in HCM because the remote myocardium could have higher signal intensity due to the higher noise.
In our study DICOM images were normalized to a 8 bit scale. This conversion allowed to obtain a curve of distribution of pixel intensity in a fixed scale from 0 to 255 in every patients. A larger grayscale (i.e. 16 bits) of pixel probably leads to more variable mean intensity and to a larger SD in ROI. However, since the curve of distribution of intensity is larger in DICOM but with a preserved proportionality the final result in image analysis is similar. Moreover, whereas the grayscale of signal intensity in DICOM image changes from patient to patient due to difference in shimming and magnetic field distortion, the conversion to a 8 bit scale permits to avoid this disadvantage and to compare signal histograms in all the patients independently from the adopted method. Using a "fixed" minimum-maximum algorithm and transforming the grayscale of intensity from 0 to 255, differences of windowing are nulled. In fact the signal intensity information stored in DICOM image were transformed in all the patients in a common grayscale: to the maximal signal intensity was always assigned a value of 255, to the minimal signal intensity a value of 0. Thus, windowing ca not influence the analysis of images and cannot modify the value of signal intensity of the voxel.
In this study LGE images were acquired with a fixed matrix and slice thickness. Different result in terms of quantification of myocardial enhancement could be found using different protocol with different slice thickness, matrix and pulse sequence. LGE images in this study showed a very low myocardial contrast-to-noise ratio as result of an appropriate choice of inversion time and suppression of myocardial signal. A worse myocardial suppression could permit to obtain higher mean signal intensity probably alter these results.
In normal patients the distribution of signal intensity in a perfectly nulled myocardium is very similar to a Rayleigh curve. In HCM the concordance between the measured curve of distribution and the Rayleigh is significantly lower. Using the maximal value of signal intensity found in the Rayleigh curve as threshold is more effective than methods that imply a fixed cut-off (SD2 and SD6 methods) for the quantification of enhanced myocardium in LGE images.
We thank all technicians of our magnetic resonance unit for technical and organisational assistance.
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