Atherosclerosis and Lipoproteins |
From the University Department of Radiology (R.A.T., C.M., J.-M.U., M.J.G., J.H.G.), Addenbrookes Hospital, Cambridge, UK; the Department of Pathology (J.H., M.J.G.), Papworth Hospital, Cambridge, UK; GlaxoSmithKline (A.B., L.W., J.B.), Translational Medicine and Technology, Addenbrookes Centre for Clinical Investigation, Addenbrookes Hospital, Cambridge, UK; and the Academic Department of Neurosurgery (R.A.T., P.J.K.), Addenbrookes Hospital, Cambridge, UK.
Correspondence to Dr Trivedi, University Department of Radiology, Addenbrookes Hospital, Cambridge, UK. E-mail rt256{at}radiol.cam.ac.uk
Background Inflammation within atherosclerotic lesions contributes to plaque instability and vulnerability to rupture. We set out to evaluate the use of a macrophage labeling agent to identify carotid plaque inflammation by in vivo magnetic resonance imaging (MRI).
Methods and Results Thirty patients with symptomatic severe carotid stenosis scheduled for carotid endarterectomy underwent multi-sequence MRI of the carotid bifurcation before and after injection of ultrasmall superparamagnetic particles of iron oxide (USPIOs). USPIO particles accumulated in macrophages in 24 of 30 plaques (80%). Areas of signal intensity reduction, corresponding to USPIO/macrophage-positive histological sections, were visualized in 24 of 27 (89%) patients, with an average reduction in signal intensity induced by the USPIO particles of 24% (range, 3.1% to 60.8%).
Conclusions USPIO-enhanced MRI can identify plaque inflammation in vivo by accumulation of USPIO within macrophages in carotid plaques.
The in vivo detection of plaque inflammation was evaluated using a macrophage labeling MRI contrast agent. Areas of focal signal loss on MRI corresponded to macrophage populations, thereby identifying inflamed plaques in 24 of 27 symptomatic individuals with severe ICA stenosis were detected and confirmed histologically.
Key Words: carotid inflammation MRI USPIO vulnerable plaque
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