TY - JOUR
T1 - Individualized MRI-Based Stroke Prediction Score Using Plaque Vulnerability for Symptomatic Carotid Artery Disease Patients (IMPROVE)
AU - Nies, Kelly P. H.
AU - Smits, Luc J. M.
AU - van Kuijk, Sander M. J.
AU - Hosseini, Akram A.
AU - van Dam-Nolen, Dianne H. K.
AU - Kwee, Robert M.
AU - Kurosaki, Yoshitaka
AU - Rupert, Iris
AU - Nederkoorn, Paul J.
AU - de Jong, Pim A.
AU - Bos, Daniel
AU - Yamagata, Sen
AU - Auer, Dorothee P.
AU - Schindler, Andreas
AU - Saam, Tobias
AU - van Oostenbrugge, Robert J.
AU - Kooi, M. Eline
N1 - Publisher Copyright:
© 2025 The Authors.
PY - 2025/8/1
Y1 - 2025/8/1
N2 - BACKGROUND: In symptomatic carotid stenosis, treatment decisions are currently primarily based on stenosis degree. We developed a clinical prediction model (Individualized Magnetic Resonance Imaging-Based Stroke Prediction Score Using Plaque Vulnerability for Patients With Symptomatic Carotid Artery Disease [IMPROVE]) incorporating the strong predictor, intraplaque hemorrhage on magnetic resonance imaging, stenosis degree, and risk factors to identify patients with high stroke risk. METHODS: IMPROVE was developed on data from 5 cohorts of 760 patients with symptomatic carotid disease on optimal medical treatment. Inclusion criteria included a recent transient ischemic attack/stroke (<6 months), magnetic resonance imaging-based information on intraplaque hemorrhage, no atrial fibrillation, and no immediate revascularization. IMPROVE was based on Cox regression using 5 expert-selected predictors and converted to 3-year ipsilateral ischemic stroke risk after internal validation. IMPROVE-based stratification was compared with care-as-usual using illustrative cutoffs: high risk was defined in IMPROVE as ≥ median 3-year IMPROVE risk, whereas in care-as-usual, it was ≥50% carotid stenosis. RESULTS: Sixty-five ipsilateral ischemic strokes occurred during a median follow-up of 1.2 years (interquartile range, 0.5-4.1). The IMPROVE model includes 5 predictors (hazard ratio [95% CI]: degree of stenosis [<50%: reference, 50%-69%: 4.54 (2.46-8.38), 70%-99% stenosis: 7.42 (3.45-15.95)]), presence of intraplaque hemorrhage [5.61 (2.92-10.77)], classification of last event [ocular: reference, cerebral: 3.72 (1.11-12.52)], male sex [1.26 (0.64-2.48)], and age [1.14 (0.84-1.55)] per 10-year increase). Internal validation revealed good accuracy (C statistic, 0.82 [95% CI, 0.77-0.87]) and no evidence of miscalibration (calibration slope, 0.93). Sensitivity for the illustrative IMPROVE cutoff was 92.6% (90.7-94.5) versus 80.6% (77.8-83.4) for care-as-usual. Specificity was 54.2% (50.7-57.8) for IMPROVE versus 52.9% (49.3-56.4) for care-as-usual. Patients stratified by IMPROVE as high risk had a higher incidence of ipsilateral ischemic stroke (24.0%) compared with the care-as-usual classification (20.7%). Among patients classified as lower-risk by IMPROVE and care-as-usual, 2.1% and 5.3%, respectively, experienced an ipsilateral ischemic stroke during follow-up. CONCLUSIONS: Using the presence of intraplaque hemorrhage on magnetic resonance imaging and 4 conventional parameters, the IMPROVE model provides accurate individual stroke risk estimates, which may facilitate stratification for revascularization after external validation.
AB - BACKGROUND: In symptomatic carotid stenosis, treatment decisions are currently primarily based on stenosis degree. We developed a clinical prediction model (Individualized Magnetic Resonance Imaging-Based Stroke Prediction Score Using Plaque Vulnerability for Patients With Symptomatic Carotid Artery Disease [IMPROVE]) incorporating the strong predictor, intraplaque hemorrhage on magnetic resonance imaging, stenosis degree, and risk factors to identify patients with high stroke risk. METHODS: IMPROVE was developed on data from 5 cohorts of 760 patients with symptomatic carotid disease on optimal medical treatment. Inclusion criteria included a recent transient ischemic attack/stroke (<6 months), magnetic resonance imaging-based information on intraplaque hemorrhage, no atrial fibrillation, and no immediate revascularization. IMPROVE was based on Cox regression using 5 expert-selected predictors and converted to 3-year ipsilateral ischemic stroke risk after internal validation. IMPROVE-based stratification was compared with care-as-usual using illustrative cutoffs: high risk was defined in IMPROVE as ≥ median 3-year IMPROVE risk, whereas in care-as-usual, it was ≥50% carotid stenosis. RESULTS: Sixty-five ipsilateral ischemic strokes occurred during a median follow-up of 1.2 years (interquartile range, 0.5-4.1). The IMPROVE model includes 5 predictors (hazard ratio [95% CI]: degree of stenosis [<50%: reference, 50%-69%: 4.54 (2.46-8.38), 70%-99% stenosis: 7.42 (3.45-15.95)]), presence of intraplaque hemorrhage [5.61 (2.92-10.77)], classification of last event [ocular: reference, cerebral: 3.72 (1.11-12.52)], male sex [1.26 (0.64-2.48)], and age [1.14 (0.84-1.55)] per 10-year increase). Internal validation revealed good accuracy (C statistic, 0.82 [95% CI, 0.77-0.87]) and no evidence of miscalibration (calibration slope, 0.93). Sensitivity for the illustrative IMPROVE cutoff was 92.6% (90.7-94.5) versus 80.6% (77.8-83.4) for care-as-usual. Specificity was 54.2% (50.7-57.8) for IMPROVE versus 52.9% (49.3-56.4) for care-as-usual. Patients stratified by IMPROVE as high risk had a higher incidence of ipsilateral ischemic stroke (24.0%) compared with the care-as-usual classification (20.7%). Among patients classified as lower-risk by IMPROVE and care-as-usual, 2.1% and 5.3%, respectively, experienced an ipsilateral ischemic stroke during follow-up. CONCLUSIONS: Using the presence of intraplaque hemorrhage on magnetic resonance imaging and 4 conventional parameters, the IMPROVE model provides accurate individual stroke risk estimates, which may facilitate stratification for revascularization after external validation.
KW - carotid artery diseases
KW - carotid stenosis
KW - magnetic resonance imaging
KW - risk
KW - stroke
UR - https://www.scopus.com/pages/publications/105005275642
U2 - 10.1161/STROKEAHA.124.050020
DO - 10.1161/STROKEAHA.124.050020
M3 - Article
C2 - 40336502
SN - 0039-2499
VL - 56
SP - 2068
EP - 2078
JO - Stroke
JF - Stroke
IS - 8
ER -