Stroke Mechanism Evolution in Intracranial Atherosclerotic Stenosis


Phase N/A Results N/A

Trial Description

Predictors of the risk of recurrent stroke for patients with symptomatic intracranial atherosclerotic stenosis (ICAS) remain unknown. The study will be to explore the stroke mechanism evolution in patients with ICAS by multi-model magnetic resonance imaging (MRI) which consists of diffusion-weighted imaging (DWI) and high-resolution MRI (HRMRI). The patients with symptomatic ICAS will undergo multi-model MRI. The baseline data, infarct patterns on DWI, and plaque features on HRMRI will be collected. The stroke mechanisms will be determined by the infarct patterns. During the 2 years follow-up, the recurrent ischemic events will be recorded. By comparing the baseline data, infarct patterns, and plaque features in patients with and without recurrent strokes, the high-risk features of patients with symptomatic ICAS will be identified. The evaluation of stroke mechanisms of patients with symptomatic ICAS will be summarized.

Detailed Description

Primary objective: to identify which plaque features on HRMRI in patients with symptomatic ICAS are related to recurrent stroke.
Secondary objectives: To compare plaque features in subgroups.
Patients enrollment please see Eligibility part.
A 3T GE (DISCOVERY MR 750, GE Healthcare, Waukesha, WI, USA) and a 3T Siemens Trio MR scanner (Siemens Healthcare, Ehrlangen, Germany) will be used in this study. The multiple sequences will include 3D time of flight (TOF) MR angiography, 3D T1-weighted imaging, proton attenuation weighted imaging, magnetization-prepared rapid acquisition with gradient-echo sequence (MPRAGE), and contrast enhancement on T1-weighted imaging.
The parameters of multiple sequences on GE MR Scanner are followed. 3D TOF: repetition time (TR) = minimum, echo time (TE) = minimum; field of view (FOV) = 240×220 mm2, matrix = 288×192, slice thickness = 2 mm, flip angle (FA) = 20, and scan time = 1:53 minutes. 3D CUBE T1: TR = 600 ms, TE = minimum, FOV = 240×220 mm2, matrix = 480×480, slice thickness = 0.8 mm, FA = NA, and scan time = 3:33 minutes. 3D CUBE PD: TR = 1500 ms, TE = 40 ms, FOV = 240×220 mm2, matrix = 384×384, slice thickness = 0.8 mm, FA = NA, and scan time = 2:40 minutes. MP RAGE: TR = minimum, TE = 3.3 ms, FOV = 240×240 mm2, matrix = 256×256, slice thickness = 0.8 mm, FA = 12, and scan time = 2:18 minutes.
The parameters of multiple sequences on Siemens MR Scanner are followed. 3D TOF: TR= 24 ms, TE = 4.32 ms; FOV = 140×140 mm2, matrix = 256×256, slice thickness = 0.9 mm, FA = 18, and scan time = 2 min 14 s. 3D SPACE T1: TR = 800 ms, TE = 22 ms, FOV = 180×168 mm2, matrix = 256×251, slice thickness = 0.8 mm, FA = NA, and scan time = 4:4 minutes. 3D SPACE PD: TR = 1700 ms, TE = 23 ms, FOV = 180×180 mm2, matrix = 320×304, slice thickness = 0.6 mm, FA = NA, and scan time = 4:25 minutes. MP RAGE: TR = 776.13 ms, TE = 5.8 ms, FOV = 144×144 mm2, matrix = 240×240, slice thickness = 1 mm, FA = 15, and scan time = 2:39 minutes.
IMAGING EVALUATION In this study, plaques will be identified as focal or diffuse but eccentric wall thickenings compared with normal vessel wall.
Plaque composition will include hemorrhage and calcification. The anatomical location of plaque will be recorded as either one of the four quadrants of the vessel wall on cross-sectional images.
Plaque that is distributed across ≥3 quadrants of the lumen perimeter will be defined as diffuse and that involving ≤2 will be defined as focal.
In this study, enhancement analysis will include both grades and patterns. Enhancement will be classified into 3 different grades: non-enhancement, mild-moderate enhancement, and strong enhancement. Mild-moderate enhancement is defined as less than that of the pituitary infundibulum. Strong enhancement is equal to or stronger than that of the pituitary infundibulum. The pattern of enhancement will be categorized as focal, heterogeneous, or homogenous.
The vessel and wall areas at the maximal lumen narrowing (MLN) site will be measured. The plaque volume will be calculated as the product of the plaque area and the thickness of the slices containing the plaque. The plaque/wall ratio was defined as the plaque area divided by wall area ×100%. The remodeling index was calculated as the ratio of the vessel area at the MLN site to that at the reference site. The reference site was selected based on the Warfarin-Aspirin Symptomatic Intracranial Disease trial method.
STROKE MECHANISMS The stroke includes hypoperfusion, perforator (branch atheromatous disease), artery-to-artery embolism, or co-existing (combinations of these ischemic mechanisms).
FOLLOW-UP At the 2 years follow-up, patients were contacted monthly by phone to determine whether any events had occurred at the first year and three months at the second year. Every three months, patients were examined face-to-face by two neurologists at the first year and every six months at the second year. The follow-up information included transient ischemic attack and ischemic stroke (in any vascular territory), brain hemorrhage, and all-cause death. If these events but death suspected, patients underwent brain computed tomography or MR imaging.


Trial Design

  • Observation: Cohort
  • Perspective: Prospective
  • Sampling: Non-Probability Sample

Trial Population

Symtomatic patients with intracranial atherosclerostic stenosis


Type Measure Time Frame Safety Issue
Primary Ischemic stroke event Three months to 2 year Yes
Secondary modified Rankin Score Three months to 1 year Yes
Secondary Magnetic Resonance Imaging sequences analysis and optimization Three months to 1 year Yes
Primary Ischemic stroke event (in the stenotic vascular territory) To 2 years
Secondary Ischemic stroke event (in the non-stenotic vascular territory) To 2 years