Identifying a high risk cardiovascular phenotype by carotid MRI-depicted intraplaque hemorrhage
Navneet Singh1, Alan R Moody, Geneviéve Rochon-Terry
1Department of Medical Imaging, Sunnybrook Health Sciences Centre, University of Toronto, 2075 Bayview Avenue, Toronto, M4N 3M5, Canada.
Abstract:
Intraplaque hemorrhage (IPH), a component of late-stage complicated plaque, identified within carotid endarterectomy surgical specimens has been recently demonstrated to predict cardiovascular (CV) events. MRI is able to depict carotid IPH. We investigated the ability of carotid MR-depicted IPH (MR-IPH) to identify high-risk CV patients. From January 2008 to April 2011, 216 patients (mean age, 67.5 years; range 31-100) referred for neurovascular MRI at an academic tertiary care centre, underwent 3T carotid MRI with adjunct 3D high-spatial-resolution coronal imaging to detect MR-IPH. Five experienced neuroradiologists made a binary decision on the presence or absence of MR-IPH. Patients' charts were reviewed blindly for demographic and CV outcomes data. Of the patients with and without MR-IPH, 62.5 % (15/24) and 19.8 % (38/192) had a composite CV event (defined as a past myocardial infarction, coronary intervention (i.e., angioplasty, stenting or bypass graft) and/or peripheral vascular disease), respectively. The odds ratio (OR) of a composite CV event in the MR-IPH group was 6.75 (Bivariable analysis, 95 % CI 2.75-16.6, p < 0.0001) and 3.25 (Multivariable regression analysis, 1.14-9.37, p = 0.028). MR-IPH had the highest OR of a prior CV event compared to other variables including age, sex, hypertension and stenosis. The OR of individual CV events was also significant: MI (3.35, 95 % CI 2.11-14.2, p < 0.01), coronary stenting (26.4, 95 % CI 8.80-79.4, p < 0.01), coronary angioplasty (21, 95 % CI 4.84-91.1, p < 0.01), and PVD (3.35, 95 % CI 1.09-10.3, p < 0.05). MR-IPH is independently associated with prior CV events in patients who are evaluated for neurovascular disease. Carotid MR-IPH, employed easily in routine clinical practice, is emerging as an indicator of systemic vascular disease and may potentially be a useful surrogate marker of CV risk including in those already undergoing neurovascular imaging.
Insights
Intraplaque hemorrhage detected by MRI (MR-IPH) in carotid arteries indicates a higher risk of cardiovascular events. This imaging finding can serve as a valuable indicator of systemic vascular disease and overall cardiovascular risk.
Area of Science:
- Cardiovascular Imaging
- Vascular Biology
- Radiology
Background:
- Intraplaque hemorrhage (IPH) in carotid plaques is linked to cardiovascular (CV) events.
- Magnetic Resonance Imaging (MRI) can visualize carotid IPH, termed MR-IPH.
- Identifying high-risk CV patients is crucial for timely intervention.
Purpose of the Study:
- To evaluate the capability of carotid MR-depicted IPH (MR-IPH) in identifying patients at high risk for CV events.
- To assess MR-IPH as a potential surrogate marker for systemic vascular disease.
Main Methods:
- 216 patients underwent 3T carotid MRI with 3D high-spatial-resolution coronal imaging to detect MR-IPH.
- Experienced neuroradiologists assessed MR-IPH presence.
- Patient charts were reviewed for demographic data and CV outcomes, including myocardial infarction, coronary interventions, and peripheral vascular disease.
Main Results:
- Patients with MR-IPH had a significantly higher incidence of composite CV events (62.5%) compared to those without (19.8%).
- MR-IPH was independently associated with prior CV events, with an odds ratio of 3.25 (p=0.028) in multivariable analysis.
- MR-IPH demonstrated the highest odds ratio for prior CV events compared to age, sex, hypertension, and stenosis.
Conclusions:
- Carotid MR-IPH is an independent predictor of prior cardiovascular events in patients undergoing neurovascular imaging.
- MR-IPH is a potential indicator of systemic vascular disease and a useful surrogate marker for CV risk.
- The easy implementation of MR-IPH in routine clinical practice makes it a valuable tool for risk stratification.
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