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Published on: June 20, 2014
Ferumoxytol-enhanced magnetic resonance imaging in acute myocarditis
Colin G Stirrat1, Shirjel R Alam1, Thomas J MacGillivray2,3
1British Heart Foundation/University Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.
Objectives:
Ultrasmall superparamagnetic particles of iron oxide (USPIO)-enhanced MRI can detect tissue-resident macrophage activity and identify cellular inflammation within tissues. We hypothesised that USPIO-enhanced MRI would provide a non-invasive imaging technique that would improve the diagnosis and management of patients with acute myocarditis.
Methods:
Ten volunteers and 14 patients with suspected acute myocarditis underwent T2, T2* and late gadolinium enhancement (LGE) 3T MRI, with further T2* imaging at 24 hours after USPIO (ferumoxytol, 4 mg/kg) infusion, at baseline and 3 months. Myocardial oedema and USPIO enhancement were determined within areas of LGE as well as throughout the myocardium.
Results:
Myocarditis was confirmed in nine of the 14 suspected cases of myocarditis. There was greater myocardial oedema in regions of LGE in patients with myocarditis when compared with healthy volunteer myocardium (T2 value, 57.1±5.3 vs 46.7±1.6 ms, p<0.0001). There was no demonstrable difference in USPIO enhancement between patients and volunteers even within regions displaying LGE (change in R2*, 35.0±15.0 vs 37.2±9.6 s-1, p>0.05). Imaging after 3 months in patients with myocarditis revealed a reduction in volume of LGE, a reduction in oedema measures within regions displaying LGE and improvement in ejection fraction (mean -19.7 mL, 95% CI (-0.5 to -40.0)), -5.8 ms (-0.9 to -10.7) and +6% (0.5% to 11.5%), respectively, p<0.05 for all).
Conclusion:
In patients with acute myocarditis, USPIO-enhanced MRI does not provide additional clinically relevant information to LGE and T2 mapping MRI. This suggests that tissue-resident macrophages do not provide a substantial contribution to the myocardial inflammation in this condition.Clinical trial registration NCT02319278; Results.
Insights
Ultrasmall superparamagnetic particles of iron oxide (USPIO)-enhanced MRI did not improve acute myocarditis diagnosis. USPIO-enhanced MRI did not provide additional information beyond standard MRI techniques for assessing myocardial inflammation.
Area of Science:
- Cardiovascular Imaging
- Magnetic Resonance Imaging
Background:
- Ultrasmall superparamagnetic particles of iron oxide (USPIO)-enhanced MRI can detect tissue-resident macrophage activity and cellular inflammation.
- Acute myocarditis diagnosis and management can benefit from non-invasive imaging techniques.
Purpose of the Study:
- To investigate if USPIO-enhanced MRI improves the diagnosis and management of acute myocarditis.
- To assess the role of tissue-resident macrophages in myocardial inflammation using USPIO-enhanced MRI.
Main Methods:
- 14 patients with suspected acute myocarditis and 10 healthy volunteers underwent 3T MRI, including T2, T2*, and late gadolinium enhancement (LGE).
- T2* imaging was performed after USPIO (ferumoxytol) infusion at baseline and 3 months to assess myocardial edema and USPIO enhancement.
- Myocardial edema and USPIO enhancement were quantified within LGE regions and the entire myocardium.
Main Results:
- Myocarditis was confirmed in 9 of 14 patients. Patients showed greater myocardial edema in LGE regions compared to volunteers (T2 value, 57.1±5.3 vs 46.7±1.6 ms, p<0.0001).
- No significant difference in USPIO enhancement was observed between patients and volunteers, even in LGE regions (change in R2*, 35.0±15.0 vs 37.2±9.6 s⁻¹, p>0.05).
- After 3 months, patients showed reduced LGE volume, decreased edema within LGE regions, and improved ejection fraction (p<0.05 for all).
Conclusions:
- USPIO-enhanced MRI does not provide additional clinically relevant information compared to LGE and T2 mapping MRI in acute myocarditis.
- Tissue-resident macrophages may not significantly contribute to myocardial inflammation in acute myocarditis.
- Standard MRI techniques remain valuable for assessing myocardial inflammation and disease progression in acute myocarditis.
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