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Segmental Wall Motion Classification in Echocardiograms Using Compact Shape Descriptors

Rationale and Objectives

Parametric shape representations of endocardial contours, obtained with principal component analysis (PCA) and the orthomax criterion, provide compact descriptors for classifying segmental left ventricular wall motion.

Materials and Methods

Endocardial contours were delineated in the left ventricular echocardiograms of 129 patients. Parametric models of these shapes were built with PCA and subsequently rotated using the orthomax criterion, producing models with local variations. Shape parameters of this localized model were used to predict the presence of wall motion abnormalities, as determined by expert visual wall motion scoring.

Results

Best results were obtained using the varimax criterion and full variance models. Although traditional PCA models needed 8.0 ± 3.0 parameters to classify segmental wall motion, only 5.1 ± 3.2 parameters were needed using the orthomax rotated models ( P < .05) to achieve similar classification accuracy. The classification space was also better behaved.

Conclusions

Orthomax rotation generates more local parameters, which are successful in reducing the complexity of wall motion classification. Because pathologies are typically spatially localized, many medical applications involving local classification should benefit from orthomax parameterizations.

Coronary artery diseases are a major cause of death in the Western world. Detection of wall motion abnormalities of the left ventricle, widely accepted as predictors for these diseases, is therefore of great clinical importance. Echocardiographic examination is often used for diagnosing these wall motion abnormalities, because of the speed of acquisition, the high spatial and temporal resolution, and the relatively low cost of the technique. A well-established method is stress echocardiography, which compares the left ventricular (LV) wall motion in images acquired at different stages of stress ( ). However, because the images are often evaluated visually, a quantitative and objective measure of wall motion is still lacking. To obtain such quantitative measures, automated analysis of LV wall motion may be preferred to currently visual, and therefore subjective, assessments.

Various quantitative measures have been proposed to assess wall motion in the literature ( ). Methods such as acoustic quantification and color kinesis ( ) observe the backscatter of the ultrasonic signal to measure the endocardial motion. Tissue Doppler imaging ( ) generates measurements of velocity, displacement, and strain/strain–rate values. These values can also be obtained using image-based speckle-tracking methods ( ), which are becoming increasingly popular. Other image-based methods use manual or automated delineations of the endocardial border to assess, for example, regional volumes, which may be of help in quantifying wall motion ( ).

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Materials and methods

Stress Echo and Visual Wall Motion Scoring

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Analysis of Endocardial Contours via Shape Models

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x=x¯+Φb, x

=

x

¯

+

Φ

b

,

where x¯ x

¯ is the average shape, and Φ is the eigenvector matrix. Typically, the number of shape modes is similar to the number of input training samples. Any new shape can be projected to this model using the pseudoinverse ( Φ −1 ) of the eigenvector matrix: b≈Φ−1(x−x¯). b

Φ

1

(

x

x

¯

)

.

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Orthomax Rotations

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Figure 1, Top row , Eigenvector matrixes of principal component analysis (PCA) and orthomax rotated shape model of the four-chamber. Bottom row , Shape variations of the fifth mode, showing localization of variation for the rotated model.

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ξ={∑kj=1∑ni=1G4ij−γn∑kj=1[∑ni=1G2ij]2}/n, ξ

=

{

j

=

1

k

i

=

1

n

G

i

j

4

γ

n

j

=

1

k

[

i

=

1

n

G

i

j

2

]

2

}

n

,

where G__ij denotes the scalar element in the i__th row and j__th column in the rotated eigenvector matrix G = ΦR , and γ is the orthomax type. The shape coefficients after rotation bR can be found with bR = R −1 b .

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∑ki=1λi≥fV, ∑

i

=

1

k

λ

i

f

V

,

where k denotes the number of eigenvectors with the largest eigenvalues λ i . Modes with low eigenvalues, corresponding with the rightmost columns of the eigenvector matrix Φ , are removed before the orthomax rotation.

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Clinical Data and Contour Delineation

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Figure 2, Left ventricular (LV) segments in four- and two-chamber views. LAD, left anterior descending artery; LCX, left circumflex artery; RCA, right coronary artery.

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Wall Motion Classification

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Results

Orthomax Rotations

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Figure 3, Global principal component analysis (PCA) and localized orthomax modes of the four-chamber model. Absolute displacements resulting from ±3 SD parameter variation are shown on the average shapes. For lower proportion of retained variance ( f ), the variations are less localized.

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Orthomax Criteria

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Table 1

Classification Accuracy of Individual Segments versus the Number of Shape Parameters Used (mean ± SD) for Different Orthomax Criteria, Averaged over Nine Segments

f Classification Accuracy Parameters TRN L-1-O TST PCA 99.9% 88.9 ± 5.9% 74.0 ± 9.4% 8.0 ± 3.0 Quartimax 99.9% 90.1 ± 5.2% 75.4 ± 9.8% 5.6 ± 3.9 ⁎ Factor parsimony 99.9% 89.4 ± 5.7% 76.3 ± 10.3% 5.4 ± 3.2 ⁎ Varimax 99.9% 91.1 ± 4.5% 76.5 ± 10.5% 5.1 ± 3.2 ⁎ 99% 88.9 ± 5.9% 76.0 ± 8.7% 5.7 ± 3.3 ⁎ 98% 87.7 ± 7.0% 75.8 ± 9.5% 6.4 ± 3.5 95% 86.3 ± 6.1% 76.3 ± 9.0% 6.6 ± 3.7

PCA, principal component analysis; TRN, training set; TST, testing set.

f denotes different proportions of retained variance in the shape models.

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Proportion of Retained Variance

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Segmental Classification

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Table 2

Classification Accuracy in Multiple Segments versus the Number of PCA and Varimax Shape Parameters Used

View Segment ( n ) Normal PCA f = 99.9% Varimax f = 99.9% Classification Accuracy # Parameters Classification Accuracy # Parameters TRN L-1-O TST TRN L-1-O TST 4C+2C All (9) 25.6% 89.2% 70.3% 11 100% 70.9% 47 4C Total 4C (5) 22.5% 87.7% 78.1% 13 96.9% 81.3% 18 2C Total 2C (5) 6.2% 100% 96.9% 21 100% 96.9% 35 4C Septal (2) 29.5% 100% 67.2% 28 92.3% 64.1% 24 4C Lateral (2) 49.6% 81.5% 70.3% 10 90.8% 70.3% 8 2C Anterior (2) 61.2% 93.8% 73.4% 11 93.8% 75.0% 14 2C Inferior (2) 30.2% 93.8% 75.0% 14 98.5% 76.6% 14 2-segment combinations: Mean 42.6% 92.3% 71.5% 15.8 93.9% 71.5% 13.8 SD 15.5% 7.8% 3.5% 8.3 3.3% 5.6% 7.3

2C, two-chamber; 4C, four-chamber; PCA, principal component analysis; TRN, training set; TST, testing set.

n denotes the number of segments combined.

The percentage of normal motion of all datasets is also listed.

Table 3

Classification Accuracy in Individual Segments versus the Number of PCA and Varimax Shape Parameters Used

View Segment Normal PCA f = 99.9% Varimax f = 99.9% Classification Accuracy # Parameters Classification Accuracy # Parameters TRN L-1-O TST TRN L-1-O TST 4C+2C Apical 34.9% 93.8% 81.3% 7 95.4% 85.9% 6 4C Septal Basal 59.7% 86.6% 70.3% 10 90.8% 64.1% 5 4C Septal Mid 42.6% 92.3% 73.4% 12 92.3% 73.4% 11 4C Lateral Basal 84.5% 86.2% 64.1% 8 90.8% 82.8% 2 4C Lateral Mid 51.2% 76.9% 69.8% 6 81.5% 71.4% 2 2C Anterior Basal 97.7% 95.4% 95.3% 3 96.9% 96.9% 2 2C Anterior Mid 61.2% 93.8% 74.6% 11 93.8% 76.2% 9 2C Inferior Basal 42.6% 84.6% 71.9% 5 90.8% 71.9% 5 2C Inferior Mid 39.5% 90.8% 65.6% 10 87.7% 65.6% 4 Mean 57.1% 88.9% 74.0% 8.0 91.1% 76.5% 5.1 ⁎ SD 21.4% 5.9% 9.4% 3.0 4.5% 10.5% 3.2

2C, two-chamber; 4C, four-chamber; PCA, principal component analysis; TRN, training set; TST, testing set.

The percentage of normal motion of all datasets is also listed.

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Figure 4, Cluster quality J is higher for varimax than principal component analysis (PCA) classification space, meaning better cluster separation. *For proportion of retained variance f = 99.9%, the improvement in J is statistically significant ( P < .05).

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Figure 5, Histogram of the modes used for classification of individual segments. Many principal component analysis (PCA) modes corresponded with large eigenvalues; no clear relation can be seen for the varimax rotated modes.

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Discussion

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Orthomax Criteria

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Proportion of Retained Variance

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Segmental Classification

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Visual Wall Motion Scoring and Alternatives

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Limitations of Study Setup

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Orthomax Extensions and Alternatives

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Conclusions

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Acknowledgments

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