Ultrasound, Fluid Dynamics Used for Predicting Plaque in Coronary Arteries
By MedImaging International staff writers Posted on 22 Aug 2011 |
Researchers have developed a method for predicting which areas of the coronary arteries will develop more atherosclerotic plaque over time, based on intracoronary ultrasound and blood flow measurements.
The method could help physicians identify “vulnerable plaque,” which unstable plaque that is likely to cause a heart attack or stroke. It involves calculating shear stress, or how hard the blood pulls on the walls of the arteries, based on the geometry of the arteries and how fast the blood is moving.
Researchers from Emory University (Atlanta, GA, USA) and Georgia Institute of Technology (Georgia Tech; Atlanta, USA) posted their findings online August 2011 in the journal Circulation. The lead author is Habib Samady, MD, professor of medicine and director of interventional cardiology at Emory University School of Medicine. Most people who have heart attacks do not have plaques in their arteries that bulge out and obstruct blood flow beforehand. Instead, the plaques in their arteries crack and spill open, leading to a clot. Dr. Samady reported that his team’s ultimate aim is to try to figure out where that will happen.
Cardiology researchers examining arteries in isolation or in animals have long seen a link between branches in the arteries, disturbances in blood flow, and where atherosclerosis develops. The challenge was to translate observations from the laboratory to imaging the heart within a live person, according to Dr. Samady. “It’s like looking at a river and predicting where sediment will accumulate,” he said. “It sounds obvious, but it’s hard to do it for every nook and cranny in the coronary arteries.”
The Emory/Georgia Tech study was the largest published investigation of shear stress and plaque progression in humans so far, and the first to examine people with significant coronary artery disease. Doctors examined 20 patients in Emory University Hospital’s catheterization laboratory between December 2007 and January 2009. They were being examined because they had abnormal exercise electrocardiograms (ECGs) or stable chest pain. The patients' coronary arteries were examined by intracoronary ultrasound and Doppler guide wire before and after six months of therapy with atorvastatin (Lipitor).
To model shear stress, Dr. Samady, assistant professor Michael McDaniel, MD, and postdoctoral fellow Parham Eshtehardi, MD, teamed up with Drs. Jin Suo and Don Giddens, experts in fluid mechanics at Georgia Tech. The patients’ arteries were divided into more than 100 segments each, and the shear stress was calculated for each one. Ultrasound allowed the researchers to estimate the size and composition of the plaques in each segment before and after the six-month period.
“Some atherosclerotic plaque appears to develop in a steady progression, and in other places, it develops in fits and spurts. These areas exist within the same patient and the same artery,” Dr. Samady stated. “Our thinking is that the places where plaque develops in more fits and spurts may lead to the rupture of plaque, leading to a clot that blocks blood flow. In contrast, the places where you have steady progression may be more stable, as long as there is a fibrous covering that is thick enough.”
Analyzing each segment, the overall area of the plaque increased and the core of the plaque grew larger in places where shear stress was particularly low. In places where the shear stress was high, there was shrinking of the fibrous covering of the plaque and expansion of lipid necrotic core and dense calcified areas. “High shear stress leads to regression, which you might think is good, but there are some bad actors that may lead to plaque rupture,” Dr. Samady said. “What’s new here is that we're seeing the detrimental effects of both low and high shear stress.”
The data also revealed that arterial plaques could grow despite anti-cholesterol therapy with statins, the current standard of care. To really assess whether plaque in a certain spot is going to be dangerous, Dr. Samady noted that physicians would need to look at outcomes in more patients over a longer period. “The dream is to predict which spot is vulnerable, and use that to guide treatment with drugs and interventions like stents,” he said.
For the present, the shear stress-based technique can be used to monitor patients’ progress and determine how well treatment is working. According to Dr. Samady, ultrasound and blood flow measurements could be combined with a newer method called optical coherence tomography for better resolution and more information.
Related Links:
Emory University
Georgia Institute of Technology
The method could help physicians identify “vulnerable plaque,” which unstable plaque that is likely to cause a heart attack or stroke. It involves calculating shear stress, or how hard the blood pulls on the walls of the arteries, based on the geometry of the arteries and how fast the blood is moving.
Researchers from Emory University (Atlanta, GA, USA) and Georgia Institute of Technology (Georgia Tech; Atlanta, USA) posted their findings online August 2011 in the journal Circulation. The lead author is Habib Samady, MD, professor of medicine and director of interventional cardiology at Emory University School of Medicine. Most people who have heart attacks do not have plaques in their arteries that bulge out and obstruct blood flow beforehand. Instead, the plaques in their arteries crack and spill open, leading to a clot. Dr. Samady reported that his team’s ultimate aim is to try to figure out where that will happen.
Cardiology researchers examining arteries in isolation or in animals have long seen a link between branches in the arteries, disturbances in blood flow, and where atherosclerosis develops. The challenge was to translate observations from the laboratory to imaging the heart within a live person, according to Dr. Samady. “It’s like looking at a river and predicting where sediment will accumulate,” he said. “It sounds obvious, but it’s hard to do it for every nook and cranny in the coronary arteries.”
The Emory/Georgia Tech study was the largest published investigation of shear stress and plaque progression in humans so far, and the first to examine people with significant coronary artery disease. Doctors examined 20 patients in Emory University Hospital’s catheterization laboratory between December 2007 and January 2009. They were being examined because they had abnormal exercise electrocardiograms (ECGs) or stable chest pain. The patients' coronary arteries were examined by intracoronary ultrasound and Doppler guide wire before and after six months of therapy with atorvastatin (Lipitor).
To model shear stress, Dr. Samady, assistant professor Michael McDaniel, MD, and postdoctoral fellow Parham Eshtehardi, MD, teamed up with Drs. Jin Suo and Don Giddens, experts in fluid mechanics at Georgia Tech. The patients’ arteries were divided into more than 100 segments each, and the shear stress was calculated for each one. Ultrasound allowed the researchers to estimate the size and composition of the plaques in each segment before and after the six-month period.
“Some atherosclerotic plaque appears to develop in a steady progression, and in other places, it develops in fits and spurts. These areas exist within the same patient and the same artery,” Dr. Samady stated. “Our thinking is that the places where plaque develops in more fits and spurts may lead to the rupture of plaque, leading to a clot that blocks blood flow. In contrast, the places where you have steady progression may be more stable, as long as there is a fibrous covering that is thick enough.”
Analyzing each segment, the overall area of the plaque increased and the core of the plaque grew larger in places where shear stress was particularly low. In places where the shear stress was high, there was shrinking of the fibrous covering of the plaque and expansion of lipid necrotic core and dense calcified areas. “High shear stress leads to regression, which you might think is good, but there are some bad actors that may lead to plaque rupture,” Dr. Samady said. “What’s new here is that we're seeing the detrimental effects of both low and high shear stress.”
The data also revealed that arterial plaques could grow despite anti-cholesterol therapy with statins, the current standard of care. To really assess whether plaque in a certain spot is going to be dangerous, Dr. Samady noted that physicians would need to look at outcomes in more patients over a longer period. “The dream is to predict which spot is vulnerable, and use that to guide treatment with drugs and interventions like stents,” he said.
For the present, the shear stress-based technique can be used to monitor patients’ progress and determine how well treatment is working. According to Dr. Samady, ultrasound and blood flow measurements could be combined with a newer method called optical coherence tomography for better resolution and more information.
Related Links:
Emory University
Georgia Institute of Technology
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