Purpose
To explore the relationship of the characteristics of symptomatic intracranial atherosclerotic plaques (ICAP) with stroke types and risk of stroke recurrence.
Methods
Patients with symptomatic intracranial atherosclerotic stenosis were prospectively enrolled. The vessel stenosis degree, plaque shape, plaque thickness, plaque burden, and plaque enhancement degree of all patients were assessed using high-resolution magnetic resonance imaging and statistically analyzed.
Results
In total, 206 patients (mean age (64 ± 12) years; 141 males) were included in this study, 154 had acute ischemic stroke (AIS), 52 had transient ischemic attack (TIA), 124 had anterior circulation ischemic symptom (ACIS), and 82 had posterior circulation ischemic symptom (PCIS). AIS patients showed higher diastolic blood pressure (t=-2.605, p = 0.011), total cholesterol (t=-2.470, p = 0.014), apolipoprotein b (z=-2.411, p = 0.016), apolipoprotein a/b (t=-2.865, p = 0.006), LDL (t=-2.424, p = 0.016), arteriosclerosis index (z=-2.256, p = 0.024), stenosis degree (t=-3.317, p < 0.001) but smaller luminal area at the plaque than TIA patients (t = 2.539, p = 0.013). In addition, 24 (13.6%) patients had stroke recurrence within 6 months. The proportion of patients with T1WI hyperintensity was higher in patients with recurrent stroke than in patients without recurrent stroke (RR = 2.592 (1.091, 6.58), χ²=4.892, p = 0.034). Patients with PCIS had greater plaque thickness (t=-4.205, p < 0.001) and remaining luminal area (z=-4.127, p < 0.001), significantly enhanced ICAP (χ²=9.681, p = 0.003), more positive remodeling (χ²=5.661, p = 0.015) and higher incidence of T1WI hyperintensity (χ²=16.472, p < 0.001) than patients with ACIS. The prevalence of diabetes (χ²=9.038, p = 0.004) in patients with PCIS is higher than that in patients with ACIS.
Conclusions
The degree of stenosis and the remaining luminal area of symptomatic ICAP are related to the type of stroke, and patients with T1WI hyperintense plaque had a higher risk of stroke recurrence within six months. Posterior circulation culprit plaque tends to have higher vulnerability, which may be related to metabolic factors secondary to diabetes.