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Structural Stability of Carotid Plaque and Symptomatology

Structural Stability of Carotid Plaque and Symptomatology

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02476396
Enrollment
176
Registered
2015-06-19
Start date
2015-11-09
Completion date
2024-07-14
Last updated
2024-08-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Carotid Artery Plaque, Carotid Artery Stenosis, Carotid Stenosis, Cerebrovascular Accident, Stroke, Transient Ischemic Attack

Brief summary

The purpose of the research is to understand structural plaque abnormalities that make a carotid plaque unstable and brake off (embolize) which would help to predict and treat individuals who are likely to suffer not only classic episodic major strokes but also cognitive impairment.

Detailed description

This study examines the relationship between the structural stability of carotid atherosclerotic plaque forming at the bifurcation of the common internal/external carotids and the ability of such lesions to cause disease. The theory behind this work is the hypothesis that carotid atherosclerotic stroke presents not only as a classical episodic clinical condition, but may also involve elements of a continuous process involving large and small vessel circulations, microcirculatory changes, cellular metabolic resistance to ischemia and micro embolic events. Recent studies suggest for every recognized clinical stroke, 5 silent strokes take place. The patient implications are enormous as imaging suggests 11 million silent strokes occur yearly in the US with poor understanding of the pathophysiology or cognitive consequences for our patients. Within this framework, the investigators choose to study the hypothesis that carotid artery atherosclerosis is likely to cause microemboli, as well as classic macroemboli, which may result in more subtle disturbances than those ordinarily detected by more obvious clinical events such as stroke and transient ischemia attacks. Understanding the structural plaque abnormalities that render a carotid plaque unstable and at risk of embolization would help to predict and treat individuals who are likely to suffer not only classic episodic major strokes, but also cognitive impairment from the contribution of microemboli to this overall disease process. The investigators have previously described a non-invasive ultrasound-based measure of plaque structural stability which will be further studied in this proposal. This study will expand on previous work performed at the University of Wisconsin-Madison, and will include patients with carotid artery stenosis, both with and without classic stroke symptoms, as well as a control group of patients without known atherosclerotic disease. Current treatments for carotid artery stenosis include either carotid endarterectomy to remove plaque or carotid stenting using a expandable metal coil to prevent the artery from narrowing. In the previous version of this protocol, the investigators have enrolled 95 -subjects (75 patient-subjects and 20 control-subjects) with no safety concerns. Findings include new understanding of the relatively of atherosclerosis and cognition as well as the basic pathophysiology of atherosclerotic large to small vessel disease. The study will run for 5 years from IRB approval with potential to further expand it. All patient-subjects will have a baseline and 1-year follow-up, ultrasound, TCD, blood collection and cognitive study to see if endarterectomy or stenting (endovascular) affected pre-op change. Change in cognition will be compared to report studies in the normal control group. In past, carotid patients have been recruited at a greater pace. Given the complexity of these studies the investigators anticipate recruitment and complete analysis of 20 patients/year. During this time initial psychological testing will be done pre-operatively. During the final year of the study, the data analysis of the plaque ultrasounds, and histopathology and 1-year follow-up the patient received in the last year of recruitment will take place. The investigators can recruit additional patients to fill any missing data points if these results identify a subset of classically asymptomatic patients with significant carotid plaques and microemboli causing vascular cognitive decline. * Specific Aim 1: Atherosclerosis, plaque elasticity, strain defects and histopathology of plaque. This aim will study the relationship of structural instability in the carotid plaques with histopathologic evidence for fissuring of the plaques that may represent a micro-emboli source. The determination of a structural defect causing abnormal strain measurements in a carotid atherosclerotic plaque will be important in understanding the pathophysiology of this disorder, as well as, addressing future treatment strategies, which could include preventing angiogenesis, thrombosis, or abnormal cholesterol deposit within the plaque. * Specific Aim 2: Plaque strain deficits and microemboli. In this aim, the investigators will preoperatively measure the structural stability of each plaque ultrasonically while simultaneously recording distally for the presence of microemboli over time within the carotid system. Statistical analysis will establish the structural instability signature that predicts ongoing subclinical microemboli. * Specific Aim 3: Plaque strain deficits, microemboli, and cognition. This aim will analyze increased elasticity strain within carotid plaques as measured preoperatively with ultrasound and correlate these parameters with cognition * Specific Aim 4: Blood RNA expression profiles can be used as biomarkers to identify the patients with a higher risk of plaque instability. This aim will analyze the mRNA and microRNA expression profiles of the blood and the excised plaque samples from patients with stable and ruptured carotid atherosclerotic plaques. The RNA analysis will be conducted with the microarrays.

Interventions

PROCEDURECarotid Endarterectomy or Stenting

Carotid endarterectomy is a procedure to treat carotid artery disease. This disease occurs when fatty, waxy deposits build up in one of the carotid arteries. The carotid arteries are blood vessels located on each side of your neck (carotid arteries). This buildup of plaques (atherosclerosis) may restrict blood flow to your brain. Removing plaques causing the narrowing in the artery can improve blood flow in your carotid artery and reduce your risk of stroke. In carotid endarterectomy, you an anesthetic. Your surgeon makes an incision along the front of your neck, opens your carotid artery and removes the plaques that are clogging your artery. Your surgeon then repairs the artery with stitches or a patch made with a vein or artificial material (patch graft). Source: Mayo Clinic Carotid stenting uses a expandable metal coil to prevent the artery from narrowing.

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH
National Institute of Neurological Disorders and Stroke (NINDS)
CollaboratorNIH
University of Wisconsin, Madison
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

(Patients): * Patients undergoing carotid endarterectomy or stenting (endovascular) for established clinical criteria * Age \> 18 years * Male or Female * English speaking * Patients must sign written informed consent form Inclusion Criteria (Controls): * A spouse or sibling of a Patient Subject * Age \> 18 years * Male or Female * English speaking * Control-Subject must sign a written informed consent form

Exclusion criteria

(Patients): * Previous history of carotid artery surgery (endovascular or open) on the same side * Previous cervical radiation * Patients not felt be suitable for carotid endarterectomy or stenting (endovascular) * Patients with impaired consent capacity * Contraindication to MRI scans (impaired renal function, need for sedative medication during scans, inability to lie in scanner for 60 minutes) * Prisoner status

Design outcomes

Primary

MeasureTime frameDescription
Change in Impairment Index - General Cognitive Morbiditybaseline (pre-surgery), 1 year follow upGeneral cognitive morbidity will be derived by comparison of the Kaufman 4-subtest IQ and NART. The NART is brief standardized test that assesses an individual's ability to read irregular words (e.g., subtle). Performance on this test has been shown to be highly correlated with years of formal education and premorbid intellectual ability as assessed by traditional intelligence tests. Performance on NART will serve as a comparison against which to compare current IQ as determined by a brief 4-subtest version of the WAIS-R. This abbreviated IQ measure has been demonstrated to have very high correlation (r \> .95) with the complete standard WAIS-R Full Scale IQ. Comparison of predicted versus obtained IQ will provide a measure of potential cognitive decline to be used in comparison of groups at study entry.
Change in Resistive index measured by transcranial Doppler (TCD)baseline (pre-surgery), 1 year follow upTCD will be utilized to acquire resistive index (RI) measurements of blood flow in the right and left middle cerebral arteries.
Histopathologic classification of carotid atherosclerotic plaque after removal for plaque ulcerationobtained day of surgeryHistologic classification of plaques is made using the updated classification of atherosclerotic plaques recommended by the American Heart association.
Change in Ultrasound Strain Measurements (Gray Scale Median Value) on Carotid Plaquesbaseline (pre-surgery), 1 year follow upUltrasound Radio frequency (RF) data will be acquired on patients, using both one-dimensional (1D) and two-dimensional (2D) wobbler and/or matrix array transducers to obtain four-dimensional (3D + time) RF data sets. The hypothesis is that plaques which have a lower gray scale median value and which during deformations of the cardiac cycles show larger stress concentrations in these regions are more vulnerable to rupture.
Change in In-vivo velocity measured by Transcranial Doppler (TCD)baseline (pre-surgery), 1 year follow upTCD will be utilized to acquire in-vivo velocity (peak systolic, mean, and end diastolic velocity information) measurements of blood flow in the right and left middle cerebral arteries.
Change in Systolic to diastolic ratio measured by transcranial Doppler (TCD)baseline (pre-surgery), 1 year follow upTCD will be utilized to acquire systolic to diastolic (S/D) ratio of blood flow in the right and left middle cerebral arteries.
Change in Pulsatility index measured by transcranial Doppler (TCD)baseline (pre-surgery), 1 year follow upTCD will be utilized to acquire pulsatility index (PI) measurements of blood flow in the right and left middle cerebral arteries.

Secondary

MeasureTime frameDescription
Change in Impairment Index - Cognitive Domain Z-scoresbaseline (pre-surgery), 1 year follow upA summary impairment index will be derived for each participant in part using composite cognitive domain z-scores (executive function, visuospatial, language, memory).
Change in Impairment Index - Number of Abnormal Test Scoresbaseline (pre-surgery), 1 year follow upThe 60-minute cognitive screen is the most thorough assessment with the greatest sensitivity to detect the cognitive disruption associated with vascular cognitive impairment (VCI). The cognitive domains to be assessed include executive function and activation, visuospatial ability, language/lexical retrieval, and memory/learning, for a total of 10 tests. A summary impairment index will be derived for each participant and include the proportion of abnormal test scores.

Other

MeasureTime frameDescription
White Matter Hyperintensity (WMH) Volumesbaseline (pre-surgery)From brain MRI scans, WMH volume will be evaluated using semi-automated segmentation of T2-FLAIR images.
Hemoglobin A1Cbaseline
Thickness of the fibrous capobtained day of surgeryExamination of fibrous cap of the atherosclerotic plaque to measure thickness.
Fasting Lipid Panelbaseline
Compare DNA between blood, plaque, and genesbaseline
High-sensitivity C-reactive protein (hs-CRP)baseline
Number of vascular channelsobtained day of surgeryHistopathologic examination of vascular channels to determine the number of channels in the fibrous cap vs the plaque proper.
Percent diameter stenosis measured with MRIbaseline (pre-surgery)The percent diameter stenosis will be determined with NASCET criteria.
Maximum Plaque Thickness measured with MRIbaseline (pre-surgery)Maximum plaque thickness was measured in the transverse plane, perpendicular to the center axis of the lumen
Number of ulcerations measured with MRIbaseline (pre-surgery)Ulceration will be determined by using a size threshold of 1 mm
Intraluminal Thrombus measured with MRIbaseline (pre-surgery)Intraluminal thrombus will be determined by a central filling defect
Thinnest area of the enhancing FCbaseline (pre-surgery)The thinnest area of the enhancing FC will be recorded with FC fissuring being defined as full thickness defects
Carotid intraplaque hemorrhage (IPH)baseline (pre-surgery)Carotid IPH will be defined by MPnRAGE-positive plaque with ≥2-fold signal compared with the sternocleidomastoid muscle
Volumetricsbaseline (pre-surgery)Total volumes of plaque, lipid-rich necrotic core (LRNC), IPH, and neovascularity will be determined quantitatively with volumes manually segmented from multi-contrast scans

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026