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Circulation, Vol 74, 1093-1098, Copyright © 1986 by American Heart Association
E Picano, L Landini, F Lattanzi, A Mazzarisi, R Sarnelli, A Distante, A Benassi and A L'Abbate
This study was designed to determine whether a quantitative analysis of
integrated backscatter amplitude distribution is potentially useful in
characterizing the atherosclerotic lesion. One hundred measurements (10 X
10 array) were made in fresh aortic regions (2 cm X 2 cm) of nine normal
and 19 atherosclerotic arterial walls. A 10 MHz transducer was used. The
integrated backscatter distinguished normal from atherosclerotic specimens
(-56.7 +/- 4.3 vs -42.5 +/- 8.9 dB, p less than .01). The shape of the
integrated backscatter amplitude distribution was analyzed by calculation
of skewness and kurtosis of each arterial region. Both skewness values
(0.134 +/- 0.325 vs -0.193 +/- 0.491 in normal and atherosclerotic
segments, respectively, p = NS) and kurtosis values (0.055 +/- 0.765 vs
-0.610 +/- 0.379, p less than .01) discriminated between the two groups.
When only the six atherosclerotic specimens with mostly fatty and
fibrofatty sites were considered, skewness and kurtosis still distinguished
normal from atherosclerotic regions (0.134 +/- 0.325 vs -0.404 +/- 0.232, p
less than .05 and 0.055 +/- 0.765 vs -0.558 +/- 0.337, p less than .05,
respectively), while integrated backscatter values did not (-56.7 +/- 4.5
vs -52.3 +/- 6.1 dB, p = NS). In conclusion, atherosclerosis may be
detected in vitro by the quantitative analysis of integrated backscatter
distribution. This variable could also be of help in the identification of
less obvious forms of atherosclerotic disease that are not distinguishable
on the basis of integrated backscatter amplitude.
ARTICLES
The use of frequency histograms of ultrasonic backscatter amplitudes for detection of atherosclerosis in vitro
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