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Published on: February 14, 2017
Carotid artery wall motion analysis from B-mode ultrasound using adaptive block matching: in silico evaluation and in
A Gastounioti1, S Golemati, J S Stoitsis
1Biomedical Simulations and Imaging Laboratory, National Technical University of Athens, Greece.
Insights
This study introduces adaptive block matching (ABM) motion estimators for improved carotid plaque risk stratification. The most effective algorithm, ABM(FIRF2), identified five novel motion-based markers to predict cerebrovascular events.
Area of Science:
- Biomedical Engineering
- Medical Imaging Analysis
- Cardiovascular Research
Background:
- Carotid atherosclerotic plaque risk stratification is vital for preventing cerebrovascular events.
- Motion analysis (MA) offers insights into arterial wall dynamics, but identifying motion-based risk markers is challenging.
- The accuracy of MA depends on motion estimators (MEs) that can adapt to changing target appearances.
Purpose of the Study:
- To investigate the potential of adaptive block matching (ABM) motion estimators for enhanced MA in carotid artery disease.
- To optimize and validate ABM algorithms within an in silico framework for MA accuracy.
- To identify novel, motion-based risk markers for carotid atherosclerotic plaques using advanced MA techniques.
Main Methods:
- Development and optimization of adaptive block matching (ABM) motion estimators, including ABM(FIRF2), within a specialized in silico framework.
- Evaluation of ABM algorithms' accuracy in motion estimation for arterial wall dynamics.
- In vivo application of the most effective ABM algorithm for identifying potential plaque-related risk markers.
Main Results:
- ABM(FIRF2) demonstrated a 47% accuracy increase over conventional block matching by leveraging arterial wall motion periodicity.
- Five potential risk markers were identified in vivo: low radial and longitudinal wall motion amplitude adjacent to plaques (RMA(PWL), LMA(PWL)), high radial motion amplitude of the plaque top surface (RMA(PTS)), and high relative radial strain (RSI(PL)) and longitudinal shear strain (LSSI(PL)) between plaque surfaces.
- In silico validated MEs, OF(LK(WLS)) and ABM(KF-K2), reproduced the in vivo findings, confirming the clinical value of the identified markers.
Conclusions:
- Adaptive block matching (ABM) motion estimators, particularly ABM(FIRF2), significantly enhance motion analysis accuracy for carotid plaques.
- Novel motion-based risk markers associated with plaque and adjacent wall dynamics have been identified, offering potential for improved cerebrovascular event prediction.
- The study validates the clinical relevance of these markers and the utility of advanced MEs, paving the way for future clinical investigations.
Abstract:
Valid risk stratification for carotid atherosclerotic plaques represents a crucial public health issue toward preventing fatal cerebrovascular events. Although motion analysis (MA) provides useful information about arterial wall dynamics, the identification of motion-based risk markers remains a significant challenge. Considering that the ability of a motion estimator (ME) to handle changes in the appearance of motion targets has a major effect on accuracy in MA, we investigated the potential of adaptive block matching (ABM) MEs, which consider changes in image intensities over time. To assure the validity in MA, we optimized and evaluated the ABM MEs in the context of a specially designed in silico framework. ABM(FIRF2), which takes advantage of the periodicity characterizing the arterial wall motion, was the most effective ABM algorithm, yielding a 47% accuracy increase with respect to the conventional block matching. The in vivo application of ABM(FIRF2) revealed five potential risk markers: low movement amplitude of the normal part of the wall adjacent to the plaques in the radial (RMA(PWL)) and longitudinal (LMA(PWL)) directions, high radial motion amplitude of the plaque top surface (RMA(PTS)), and high relative movement, expressed in terms of radial strain (RSI(PL)) and longitudinal shear strain (LSSI(PL)), between plaque top and bottom surfaces. The in vivo results were reproduced by OF(LK(WLS)) and ABM(KF-K2), MEs previously proposed by the authors and with remarkable in silico performances, thereby reinforcing the clinical values of the markers and the potential of those MEs. Future in vivo studies will elucidate with confidence the full potential of the markers.
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