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2012 Proceedings - International Tissue Elasticity Conference

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066 COMBINED ULTRASOUND ELASTICITY AND THERMAL STRAIN IMAGING FOR<br />

COMPREHENSIVE ASSESSMENT OF ATHEROSCLEROTIC PLAQUE IN A RABBIT MODEL.<br />

A Mahmoud 1,2 , D Dutta 1 , L Lavery 1 , K Kim 1,3,4 – Presented by JM Rubin .<br />

1 Center for Ultrasound Molecular Imaging and Therapeutics, Heart and Vascular Institute,<br />

University of Pittsburgh Medical Center, Pittsburgh, PA, USA; 2 Bioengineering Department, Cairo<br />

University, Giza, EGYPT; 3 Bioengineering Department, University of Pittsburgh, Pittsburgh, PA,<br />

USA; 4 McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, PA, USA.<br />

Background: Atherosclerosis imposes both mechanical and compositional changes in the vascular wall<br />

leading to the formation of atherosclerotic plaque (AP) [1]. We hypothesize that ultrasound (US) elasticity<br />

imaging (UEI) is able to assess the vascular wall mechanical property changes via measuring local strain<br />

distributions, while US thermal strain imaging (TSI) can identify lipids in the vascular wall, and combining<br />

these two techniques along with US B–mode morphology imaging can therefore provide more comprehensive<br />

information for diagnosis and monitoring of atherosclerosis development and AP vulnerability.<br />

Aims: The aims of this study are: 1) demonstrate in vivo feasibility of the combined UEI–TSI technique<br />

assessing the mechanical and compositional characteristics of AP using atherosclerotic rabbit model, and<br />

2) correlate the UEI–TSI findings with histology.<br />

Methods: AP was induced to a group of New Zealand white rabbits (n=6) by introducing a balloon injury<br />

to the femoral artery while administering high–fat high–cholesterol diet. Optimal US beamforming,<br />

imaging–heating sequence, heating US transducer and electronics were designed and integrated to<br />

commercial US scanners including a clinical system (SonixTOUCH, Ultrasonix Medical Corp., Canada) and a<br />

high–resolution small animal imaging system (Vevo2100, VisualSonics Inc., Canada). US duplex was used to<br />

localize atherosclerotic lesions. US radiofrequency (RF) frames were acquired for approximately 2 seconds for<br />

UEI, followed by 8 second RF capturing for US–TSI while heating transducer was operated to induce a slight<br />

temperature rise ( ≤2ºC) within the safe range according to the American Institute of Ultrasound in Medicine.<br />

ECG was used to trigger TSI frame acquisition per the QRS complex and assure eliminating the mechanical<br />

strain effect. A 2D phase-sensitive speckle tracking was applied to estimate mechanical strains for UEI due to<br />

inter–cardiac pulsation and thermal strains for TSI due to sound speed changes by temperature rise. UEI and<br />

TSI strain maps, co–registered to B–mode images, were compared to Oil–Red–O histology.<br />

Results: Lipid–rich lesions exhibited average total compressional strain of approximately -0.44% over the<br />

systolic phase, higher than that observed in normal areas in vascular wall. That correlates well with the<br />

known elastic characteristics of soft lipid–rich lesions. Whereas in TSI, lipids showed a distinct positive<br />

strains (≈+0.18%) in AP upon the slight temperature increase, and negative, or zero, strains in th e<br />

surrounding water–based tissues. UEI and TSI findings showed good agreement with histology.<br />

Conclusions: The combined UEI–TSI imaging technique was able to assess successfully both mechanical<br />

and compositional characteristics of AP in the femoral artery of atherosclerotic rabbit model in vivo. The<br />

co–registered complete set of morphological, mechanical, and compositional information obtained by the<br />

UEI–TSI imaging correlated well with histological findings. This combined UEI–TSI can be relatively easily<br />

implemented into commercial US systems with minimal modification to complement other modalities in<br />

diagnosing and assessing AP vulnerability in clinics in the future.<br />

Acknowledgements: This study was supported in part by NIH 1R01HL098230–01A1 (PI: Kim). Small animal imaging<br />

system (Vevo2100) was supported through NIH 1S10RR027383–01 (PI: Kim).<br />

References:<br />

[1] Virmani R, Narula J, Leon MB, Willerson JT: The Vulnerable Atherosclerotic Plaque: Strategies for Diagnosis and<br />

Management. First edition, Wiley–Blackwell, 2006.<br />

Figure 1: Ultrasound in vivo images including Doppler, UEI and TSI compared well with Oil–Red–O histology in assessing<br />

atherosclerotic plaque (red arrows) developed in rabbit femoral artery 10 weeks after balloon injury.<br />

indicates Presenter 109

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