Related Experiment Video
Updated: Nov 17, 2025

High-Resolution Cardiac Positron Emission Tomography/Computed Tomography for Small Animals
Published on: December 16, 2022
Predicting the clinical course in hypertrophic cardiomyopathy using thallium-201 myocardial scintigraphy
Mareomi Hamada1, Yuji Shigematsu2, Shigeru Nakata3
1Division of Cardiology, Uwajima City Hospital, 1-1 Goten-machi, Uwajima, Ehime, 798-8510, Japan.
Insights
Thallium-201 scintigraphy reveals significant left ventricular remodelling in hypertrophic cardiomyopathy (HCM) patients over time. The mean count change (MCC) metric may offer superior evaluation of these myocardial perfusion changes compared to the extent score (ES).
Area of Science:
- Cardiology
- Nuclear Medicine
- Medical Imaging
Background:
- Hypertrophic cardiomyopathy (HCM) is a complex cardiac condition.
- Left ventricular remodelling is a key feature of HCM.
- Monitoring remodelling progression is crucial for patient management.
Purpose of the Study:
- To evaluate temporal changes in left ventricular remodelling in HCM patients.
- To assess the utility of thallium-201 myocardial scintigraphy in tracking these changes.
- To compare the effectiveness of the extent score (ES) and mean count change (MCC) indices.
Main Methods:
- Forty-eight HCM patients underwent thallium-201 myocardial scintigraphy.
- Myocardial perfusion defects were quantified using extent score (ES) and mean count change (MCC).
- Left ventricle was segmented to identify lesion sites; follow-up averaged 8.6 years.
Main Results:
- Significant increases in both ES (17.4% to 44.0%) and MCC (0% to 12.0%) were observed (P < 0.0001).
- The apex was the most common site for myocardial perfusion defects.
- Higher ES and MCC values correlated with left ventricular heart failure (LVHF) and associated complications like atrial fibrillation and apoplexy.
Conclusions:
- Thallium-201 myocardial scintigraphy effectively detects myocardial damage severity and lesion location in HCM.
- The mean count change (MCC) metric shows promise for superior evaluation of temporal changes in myocardial perfusion.
- These findings aid in understanding HCM progression and managing associated cardiovascular risks.
Aims:
This study aimed to evaluate the changes in left ventricular remodelling with time in patients with hypertrophic cardiomyopathy (HCM) using thallium-201 myocardial scintigraphy.
Methods And Results:
Forty-eight patients with HCM participated in the study. The extent score (ES) and a newly devised index termed the 'mean count change' (MCC) were used to evaluate the myocardial perfusion defects. Using the amount of thallium-201 uptake (TU), MCC (%) was calculated using the following formula: (last TU - initial TU)∕initial TU × 100. To confirm the site of the lesion, the left ventricle was divided into five segments: anterior, septal, inferior, lateral, and apex. Cardiovascular complications and deaths were recorded. The mean follow-up period was 8.6 ± 2.0 years. ES increased from 17.4 ± 13.7% to 44.0 ± 22.3% (P < 0.0001). MCC increased from 0% to 12.0 ± 9.0% (P < 0.0001). The apex was the most frequent site of lesion. Twenty-seven patients (56.3%) had experienced left ventricular heart failure (LVHF). Both ES and MCC were greater in patients with LVHF than in those without LVHF. An overlap between the two groups was greater in ES than in MCC. Patients with LVHF had a higher incidence of atrial fibrillation and apoplexy. Nineteen patients (39.6%) died during the study period; 14 died from LVHF, 3 from sudden cardiac death, and 2 from cancer.
Conclusions:
Thallium-201 myocardial scintigraphy is useful for detecting the severity of myocardial damage and for confirming the lesion site in patients with HCM. MCC may be superior to ES in the evaluation of these changes with time.
Related Concept Videos
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Acute Coronary Syndrome III: Diagnostic Studies
Mitral Stenosis II: Clinical features and Diagnostic Tests
Myocarditis II: Clinical Features and Diagnostic Tests
Imaging Studies for Cardiovascular System V: CT
Cardiomyopathy II: Dilated Cardiomyopathy

