PhD Seminar: Ultrasound Imaging Innovations for Visualization and Quantification of Vascular BiomarkersExport this event to calendar

Friday, August 2, 2019 — 1:00 PM EDT

Candidate: Yat Shun Yiu

Title: Ultrasound Imaging Innovations for Visualization and Quantification of Vascular Biomarkers

Date: August 2, 2019

Time: 1:00 PM

Place: EIT 3141

Supervisor(s): Yu, Alfred C.H.

 

Abstract:

More than 25% of the adult population has carotid atherosclerosis that could lead to major cerebrovascular diseases such as stroke and dementia, which are leading causes of death and serious long-term disability worldwide. Accordingly, the prevention and management of carotid atherosclerosis may play a significant role in reducing the morbidity and mortality of stroke and dementia. Current carotid atherosclerotic risk assessments rely on traditional cardiovascular risk factors that cannot accurately assess individual risk. It has been posited that this risk assessment performance may be improved by incorporating vascular biomarkers that have direct correlation to the initiation and progression of atherosclerosis. Nonetheless, it is not trivial to measure these vascular biomarkers routinely and consistently as current imaging techniques have limited spatial and temporal resolutions to derive these vascular biomarkers.

 

The goal of this thesis is to devise a new non-invasive imaging framework that can consistently quantify and visualize vascular biomarkers known to be directly related to atherosclerosis. Its overall hypothesis is that vascular biomarkers can be quantified and visualized using high-frame-rate ultrasound (HiFRUS) imaging that can generate images at more than 1000 frames per second. The corresponding sub-millisecond time resolution of HiFRUS can consistently track the spatiotemporal dynamics of blood flow in arteries, hence enabling the derivation of atherosclerotic vascular biomarkers. Based on such premise, this thesis presents three new HiFRUS algorithms that collectively form the new imaging framework to quantify atherosclerotic vascular biomarkers.

 

The first HiFRUS algorithm is called Doppler ultrasound bandwidth imaging (DUBI) that focus on measuring Doppler bandwidth to quantify and visualize unstable arterial flow, which is a contributing factor to the initiation and progression of atherosclerotic lesions. Results demonstrated that DUBI can effectively detect and visualize the differences in Doppler bandwidth between stable flow and unstable flow. Receiver operating characteristic analysis also showed that DUBI has better sensitivity and specificity in identifying unstable flow than conventional method (0.72 & 0.83 vs 0.68 & 0.66). This algorithm allows the overall imaging framework to obtain new diagnostic information relevant to atherosclerosis.

 

Motion-resistant microvascular imaging (MRMVI), the second algorithm, was devised to consistently map microvessels by suppressing the artifact caused by tissue motions such as arterial distension. Results showed that MRMVI can consistently map 50 µm diameter micro-flow channels in the presence of tissue motions, with the help of ultrasound contrast agent. The efficacy of MRMVI was further demonstrated by mapping an in vivo microvessel network with much finer detail than conventional power Doppler technique. This finding suggests that MRMVI can potentially be used to map intraplaque microvasculature to identify plaque neovascularization that is a prominent feature in advanced atherosclerotic plaque and reportedly is a predictor of future cerebrovascular events.

 

An instantaneous volumetric flow rate estimator (IVFRE, the third algorithm) was developed to measure cerebral blood flow (CBF), since atherosclerosis is suggested to place extra burden onto the already declining CBF in older adults and may lead to mild cognitive impairment and, potentially, dementia. The IVFRE algorithm first made use of the change in correlation of flow speckle over time to derive the flow flux and then compute the final blood flow rate by integrating the flow flux across the cross section of the target vessel. Results from pilot study demonstrated that IVFRE can measure blood flow rate consistently under different in vivo scenarios. IVFRE addressed the need of a tool to routinely quantify CBF for atherosclerosis evaluation and it can potentially facilitate the identification of substantial CBF reduction in patients with carotid plaque before the development of cognitive impairment and dementia.

 

Overall, this thesis has reported a series of engineering innovations to achieve a HiFRUS imaging framework that can assess new vascular biomarkers for risk stratification of carotid atherosclerosis and evaluation of the impact of atherosclerosis on CBF. It is anticipated that this framework can improve the atherosclerotic risk stratification process to more timely identify at-risk individuals. Furthermore, this framework may be used to derive new insights on the pathophysiology of carotid atherosclerosis that would aid future disease management and personalization of treatment strategies.

Location 
EIT
Room 3141
200 University Avenue West

Waterloo, ON N2L 3G1
Canada

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