Molecular imaging provides insight on cardiovascular illness
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Cardiovascular disorders continue to affect millions of individuals in the U.S., prompting researchers to identify techniques to promote early detection and provide immediate treatment. A study presented at the 58th Annual Meeting of the Society of Nuclear Medicine has suggested that molecular imaging can help determine the cause of hypertrophic cardiomyopathy (HCM), which is characterized by a thickening of the heart muscle.
Lead author Stefan Timmer and his colleagues reported that genetic mutations - such as one called MYBPC3 - could be responsible for the development of this disease.
They evaluated 16 HCM patients with this mutation, using positron emission tomography (PET) scans in order to gauge the oxygen usage of the heart. They found that individuals with MYBPC3 had less efficient hearts due to the thickening of the myocardium.
"This study shows that molecular imaging has great potential for clinical use in the field of cardiology," Timmer concluded.
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