BACKGROUND: Worldwide, 2 million patients aged 18-50 years suffer an ischemic stroke each year with an increasing trend over the past decade due to yet unknown reasons. Whereas prognosis and antithrombotic treatment in older patients with cardiovascular disease are among the best studied topics in clinical medicine, this does not hold true for patients at young age. It is of great importance to treat these patient groups correctly to prevent recurrence and bleeding complications. However, previous research have shown that there is a long-term increased risk of recurrent ischemic events despite the secondary prevention and a subsequent increased bleeding risk. To tailor effective antithrombotic therapy to the individual patient, it is essential to understand the underlying pathogenesis and identify modifiable risk factors in young patients for recurrence or bleeding. It is thought that abnormalities of hemostasis may play a key role in early-onset ischemic stroke. First, prothrombotic conditions are associated with an increased risk for ischemic stroke at young age. In addition, disturbance of the hemostatic balance due to one or several triggers can activate the coagulation cascade, which on its turn can lead or contribute to clot formation and subsequent arterial occlusion. In previous study, there were indications that trigger factors such as fever and/or an infection in the days prior to the stroke may play a role in the pathogenesis. This suggests that an interaction between inflammation, endothelial damage and coagulation may lead to the formation of a clot. In this observational study we aim to investigate the role of the immune system, endothelial damage and coagulation in the pathogenesis and prognosis of stroke in young patients. OBJECTIVE: To investigate the role of hemostasis, inflammation and endothelial activation in the etiology and prognosis in an acute ischemic stroke (or TIA) in young stroke patients. STUDY DESIGN: Multicentre prospective observational study STUDY POPULATION: All patients aged between 18 and 50 years old with a first-ever ischemic stroke or TIA who are admitted to the neurology ward or seen at the outpatient clinic of one of the participating centers. Main exclusion criteria are: history of clinical TIA, ischemic stroke or intracerebral hemorrhage. A intracerebral hemorrhage resulting from trauma, known aneurysm or underlying intracerebral malignancy. A venous infarction, retinal infarction and amourosis fugax. Inadequate control of the Dutch language to reliably sign an informed consent from and/or participate in the follow-up. Patients are excluded if they have a contra indication for 3T MRI. In addition 60 healthy controls (18-50 years old) will be included. MAIN STUDY ENDPOINTS: 1. Baseline and 3 months coagulation profile: Whole blood and platelet poor plasma thrombin generation, platelet function tests, and coagulation biomarkers, screening for thrombophilia. 2. Baseline and 3 months inflammation/endothelial activation profile: Cytokines/chemokines, expression of receptors/cofactors related to hemostasis on peripheral blood mononuclear cells (PBMCs), stimulation tests of PBMC's to assess trained immunity. 3. Vessel wall enhancement on 3 Tesla MRI 4. Questionnaire trigger factors
Study Type
OBSERVATIONAL
Enrollment
280
Radboudumc
Nijmegen, Gelderland, Netherlands
RECRUITINGCatharina Ziekenhuis
Eindhoven, North Brabant, Netherlands
NOT_YET_RECRUITINGMedisch Spectrum Twente
Enschede, Overijssel, Netherlands
NOT_YET_RECRUITINGIsala
Zwolle, Overijssel, Netherlands
NOT_YET_RECRUITINGHagaZiekenhuis
The Hague, South Holland, Netherlands
NOT_YET_RECRUITINGMedisch Centrum Leeuwarden
Leeuwarden, Netherlands
NOT_YET_RECRUITINGDifference of concentration biomarkers and coagulation assays between patients and controls
Biomarkers and assays of coagulation, inflammation and endothelium activation
Time frame: At baseline and 3 month visit
Nonfatal or fatal recurrent cardiovascular (ischemic) events
Ischemic stroke or transient ischemic attack, acute coronary syndrome, peripheral artery disease
Time frame: 10 years
Recurrent venous thrombotic events
Deep venous thrombosis, pulmonary embolism, cerebral venous sinus thrombosis
Time frame: 10 years
Death from any cause
Time frame: 10 years
Malignancy
Time frame: 10 years
Bleeding complications
Minor and major bleeding complications
Time frame: 10 years
Vessel wall imaging on 3T MRI
Detection of vessel wall enhancement on MRI in young stroke patients
Time frame: At baseline
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