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Assessment of Carotid Plaque Inflammation in Diabetic and Nondiabetic Patients-An Exploratory Ultrasmall Superparamagnetic Iron Oxide-Enhanced Magnetic Resonance Imaging Study.

Accepted version
Peer-reviewed

Type

Article

Change log

Authors

Usman, Ammara 
Patterson, Andrew J 
Sadat, Umar 
Tang, Tjun Y 
Graves, Martin J 

Abstract

BACKGROUND: Ultrasmall superparamagnetic iron oxide (USPIO)-enhanced magnetic resonance (MR) imaging enables the identification of inflammation within the atheroma, predominantly by USPIO uptake by macrophages present in atherosclerotic tissue. Diabetic patients, however, may have dysfunctional macrophage activity, which may affect utilization of USPIO in identifying plaque inflammation in this patient cohort. METHODS: Fifteen diabetic and fifteen nondiabetic patients underwent USPIO-enhanced carotid MR imaging using 1.5T MR system. Pre- and post-USPIO carotid MR images were manually coregistered. The percentage decrease in the signal intensity after USPIO administration was calculated as a relative measure of the USPIO uptake. RESULTS: Diabetic and nondiabetic patients had comparable demographics and comorbidities. The mean global, maximum quadrant, and maximum slice changes showing change in relative signal intensity as a result of USPIO administration were comparable for the two patient cohorts (P > .05). CONCLUSIONS: USPIO can identify inflammatory burden with carotid atheroma in both diabetic and nondiabetic patients.

Description

Keywords

Atherosclerosis, MRI, USPIO, carotid, nanoparticles, Aged, Carotid Stenosis, Dextrans, Diabetes Mellitus, Electrocardiography, Female, Humans, Image Processing, Computer-Assisted, Inflammation, Magnetic Resonance Angiography, Magnetic Resonance Imaging, Magnetite Nanoparticles, Male, Middle Aged, Statistics, Nonparametric

Journal Title

J Stroke Cerebrovasc Dis

Conference Name

Journal ISSN

1052-3057
1532-8511

Volume Title

26

Publisher

Elsevier BV
Sponsorship
TCC (None)
British Heart Foundation (None)
British Heart Foundation (None)
European Commission (224297)
AU is funded by Mountbatten Cambridge International Scholarship, in collaboration with Cambridge Trust, Christ’s College, and Sir Ernest Cassel Educational Trust. This study was supported by NIHR Biomedical Research Centre.