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Updated: Jun 26, 2026

A Methodological Approach to Non-invasive Assessments of Vascular Function and Morphology
Published on: February 7, 2015
Quantifying carotid plaque component regional strain using ultrasound elastography and its association with blood
Jian Cai1, Feihong Yu2, Shumei Miao2,3
1School of Biomedical Engineering and Informatics, Nanjing Medical University, Nanjing, China.
Insights
This pilot study shows ultrasound elastography can measure plaque strain, finding blood pressure influences plaque mechanics. These findings may aid in developing new models for predicting cardiovascular disease risk.
Area of Science:
- Cardiovascular Medicine
- Biomedical Engineering
- Medical Imaging
Background:
- Cardiovascular and cerebrovascular diseases are leading global causes of death.
- Carotid plaque rupture is a key factor in these diseases.
- Ultrasound elastography assesses plaque mechanics, but dynamic strain and blood pressure correlations are unclear.
Purpose of the Study:
- To investigate the dynamic strain of carotid plaque component regions using ultrasound elastography.
- To explore the correlation between regional plaque strain and blood pressure.
- To validate the feasibility of dynamic strain quantification in plaque components.
Main Methods:
- Retrospective analysis of carotid ultrasound elastography images from 11 patients.
- Image preprocessing included wavelet Bayesian denoising and enhanced correlation coefficient registration.
- Dense optical flow and regional strain were computed using the Farneback algorithm and spatial gradient extraction.
Main Results:
- Significant heterogeneity in strain was observed across plaque component regions.
- Mean inter-frame strain ranged from 0.0007 to 0.0045.
- Diastolic blood pressure positively correlated with strain indices (r=0.5121 to 0.4606).
- Pulse pressure negatively correlated with strain indices (r=-0.5043 to -0.4650).
Conclusions:
- Blood pressure may influence the mechanical environment within carotid plaque regions.
- Dynamic strain quantification of plaque components using ultrasound elastography is feasible.
- Findings suggest new avenues for studying plaque progression and non-invasive risk prediction.
Abstract:
Cardiovascular and cerebrovascular diseases are leading causes of mortality worldwide, with carotid plaque rupture being a critical pathogenic mechanism. While ultrasound elastography can assess the mechanical properties of plaque, the dynamic strain of specific plaque component regions and its correlation with blood pressure are not well characterized. This pilot study retrospectively analyzed carotid ultrasound elastography images from 11 patients. Image preprocessing involved wavelet Bayesian denoising and enhanced correlation coefficient registration to minimize motion artifacts. Dense optical flow was computed using the Farneback algorithm, and regional strain was derived through spatial gradient extraction and least-squares fitting. Our analysis revealed substantial heterogeneity in strain among plaque component regions. The mean inter-frame strain ranged from 0.0007 to 0.0045, the maximum inter-frame strain from 0.0025 to 0.0454, and the maximum cumulative strain over the cardiac cycle from 0.0078 to 0.1948. Diastolic blood pressure showed positive correlations with the mean inter-frame strain, the maximum cumulative strain and the maximum inter-frame strain of plaque component regions (r = 0.5121, 0.4606, 0.3977), the pulse pressure demonstrated moderate negative correlations with all three strain indices (r = -0.5043, -0.4757, -0.4650), showing statistical significance even with a small sample size. These exploratory findings suggest that blood pressure may influence the mechanical environment of plaque component regions. This pilot study validates the feasibility of dynamic strain quantification for plaque component regions using ultrasound elastography. The identified association with blood pressure provides new directions for investigating mechanical factors in plaque progression and developing non-invasive risk prediction models.
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