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Differentiation of Atherosclerotic Carotid Plaque Components With Dual-Energy Computed Tomography
Mueez Aizaz1, Juul Bierens, Marion J J Gijbels
1From the Department of Radiology and Nuclear Medicine, Maastricht University Medical Center, Maastricht, the Netherlands (M.A., J.B., T.F., A.A.P., M.E.K.); CARIM, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, the Netherlands (M.A., J.B., M.J.J.G., W.H.M., R.J.v.O., M.E.K.); Department of Pathology, Maastricht University Medical Center, Maastricht, the Netherlands (M.J.J.G.); Department of Medical Biochemistry, Amsterdam Cardiovascular Sciences: Atherosclerosis & Ischemic Syndrome; Amsterdam Infection and Immunity: Inflammatory Diseases; Amsterdam UMC Location University of Amsterdam, Amsterdam, the Netherlands (M.J.J.G.); Department of Neurology, Zuyderland Medical Center, Heerlen, the Netherlands (T.H.C.M.L.S.); Department of Neurology, Zuyderland Medical Center, Sittard, the Netherlands (N.P.v.O.); Department of Vascular Surgery, Maastricht University Medical Center, Maastricht, the Netherlands (J.-W.H.C.D.); Department of Clinical Neurophysiology, Maastricht University Medical Center, Maastricht, the Netherlands (W.H.M.); Department of Neurology, Maastricht University Medical Center, Maastricht, the Netherlands (R.J.v.O.); and School for Mental Health and Neuroscience (MHeNs), Maastricht University, Maastricht, the Netherlands (A.A.P.).
Objectives:
Carotid plaque vulnerability is a strong predictor of recurrent ipsilateral stroke, but differentiation of plaque components using conventional computed tomography (CT) is suboptimal. The aim of our study was to evaluate the ability of dual-energy CT (DECT) to characterize atherosclerotic carotid plaque components based on the effective atomic number and effective electron density using magnetic resonance imaging (MRI) and, where possible, histology as the reference standard.
Materials And Methods:
Patients with recent cerebral ischemia and a ≥2-mm carotid plaque underwent computed tomography angiography and MRI. A subgroup underwent carotid endarterectomy. Trained observers delineated plaque components on histology or MRI, independent of computed tomography angiography. DECT was coregistered with MRI and/or histology. Intraplaque hemorrhage (IPH), lipid-rich necrotic core (LRNC), fibrous tissue, and calcifications were delineated on DECT, and ρ eff and Z eff values were determined in the derivation cohort (n = 55). Spatial separation of these components was evaluated in a ρ eff -Z eff -cluster plot. Ranges that optimally differentiate plaque features were determined. For validation, plaque components were quantified in the validation cohort (n = 29) using these ρ eff -Z eff ranges and literature-based Hounsfield unit (HU) ranges and correlated to MRI volumes.
Results:
Eighty-four participants (68 ± 8 years; 55 male) were evaluated. In the derivation cohort, plaque components were well separated on the cluster plot, resulting in the following ranges: IPH:ρ eff < 1.15, Z eff < 7.5, LRNC:ρ eff < 1.15, Z eff :7.5-8.75, fibrous tissue:ρ eff < 1.15, Z eff > 8.75, and calcifications: ρ eff > 1.15, Z eff > 0. In the validation cohort, significant correlations were found between ρ eff -Z eff -based and MRI plaque volumes for fibrous tissue ( r = 0.69, P < 0.001), LRNC ( r = 0.94, P < 0.001), IPH ( r = 0.35, P = 0.03), and calcifications ( r = 0.70, P < 0.001). Lower correlations were found between HU-based and MRI plaque volumes for fibrous tissue ( r = 0.40, P = 0.02), LRNC ( r = 0.86, P < 0.001), and calcifications ( r = 0.47, P = 0.005), with no correlation for IPH ( r = 0.02, P = 0.45).
Conclusions:
We determined ρ eff -Z eff ranges for plaque assessment. ρ eff -Z eff -based volumes showed strong-to-very strong correlations with MRI for LRNC, fibrous tissue, and calcifications and a weak correlation for IPH. ρ eff -Z eff -based volumes demonstrated superior agreement with MRI for all plaque components compared with HU-based volumes, highlighting the potential of DECT for the identification of patients with vulnerable plaques.
