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Updated: May 16, 2026

In Vivo Quantitative Assessment of Myocardial Structure, Function, Perfusion and Viability Using Cardiac Micro-computed Tomography
Published on: February 16, 2016
Myocardial infarction in sickle cell disease: use of translational imaging to diagnose an under-recognized problem
Paul Chacko1, Eric H Kraut, Jay Zweier
1Davis Heart and Lung Research Institute, The Ohio State University, 473 W. 12th Ave, Suite 200, Columbus, OH, 43210, USA.
Insights
Sickle cell disease (SCD) can cause heart problems like myocardial infarction (MI) due to microvascular issues. Cardiac MRI (CMR) effectively detects this cardiac microvascular obstruction in SCD patients with chest pain.
Area of Science:
- Cardiology
- Hematology
- Medical Imaging
Background:
- Sickle cell disease (SCD) is an inherited blood disorder causing microvascular occlusion and multi-organ complications.
- Myocardial ischemia and infarction (MI) are potential complications of SCD, but their incidence and cause are not well understood.
- Atherosclerotic lesions are typically absent in SCD patients experiencing MI, suggesting a microvascular etiology.
Purpose of the Study:
- To investigate the utility of Cardiac Magnetic Resonance (CMR) in diagnosing microvascular disease in symptomatic SCD patients.
- To highlight the role of CMR in identifying cardiac microvascular obstruction in SCD.
- To underscore the under-recognized nature of myocardial injury in SCD.
Main Methods:
- Case demonstrations illustrating the application of CMR in SCD patients presenting with chest pain.
- Qualitative assessment of CMR's ability to depict cardiac microvascular obstruction.
Main Results:
- CMR successfully visualized cardiac microvascular obstruction in SCD patients with chest pain.
- The study demonstrated instances where CMR identified myocardial injury that might otherwise be overlooked.
- The findings emphasize CMR's unique capability in this patient population.
Conclusions:
- Cardiac MRI is a valuable tool for assessing myocardial injury in sickle cell disease patients with chest pain.
- Further research is needed to establish prevalence, detection, and management strategies for ischemic heart disease in SCD.
- Developing risk assessment tools and management algorithms may help reduce sudden cardiac death in SCD.
Abstract:
Sickle cell disease (SCD) is an inherited disorder in which microvascular occlusion causes complications across multiple organ systems. The precise incidence of myocardial ischemia and infarction (MI), potentially under-recognized microvascular disease-related complications, remains unknown. The absence of typical atherosclerotic lesions seen in other patients with MI suggests a microvascular mechanism of myocardial injury. Cardiac magnetic resonance (CMR) can demonstrate microvascular disease, making it an appealing modality to assess symptomatic SCD patients. We demonstrate in several dramatic instances how CMR is uniquely able to depict cardiac microvascular obstruction in patients with SCD and chest pain, without which the possibility of myocardial injury would almost certainly be otherwise neglected. Much remains unknown regarding ischemic heart disease in patients with SCD including prevalence, detection, and management. Further work to define evaluation and management algorithms for chest pain in SCD and to develop risk assessment tools may reduce sudden cardiac death in this population.
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