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Multiple Silent Lacunes Are Associated with Recurrent Ischemic Stroke.
Søren Due Andersen1, Flemming Skjøth, Yousef Yavarian
1Aalborg Thrombosis Research Unit, Department of Clinical Medicine, Faculty of Health, Aalborg University, Aarhus, Denmark.
Silent lacunes, small brain lesions, increase the risk of recurrent ischemic stroke in patients without atrial fibrillation (AF). Multiple silent lacunes significantly elevate this risk, while not impacting death or cardiovascular events.
Area of Science:
- Neurology
- Neuroimaging
- Stroke Medicine
Background:
- Silent lacunes are common incidental findings in ischemic stroke patients.
- Their prognostic value regarding future cardiovascular events remains unclear.
- This study investigates silent lacunes in ischemic stroke patients without atrial fibrillation (AF).
Purpose of the Study:
- To determine the association between silent lacunes and the risk of ischemic stroke recurrence.
- To evaluate the impact of silent lacunes on mortality and cardiovascular events.
- To analyze these associations in a cohort of ischemic stroke patients excluding those with AF.
Main Methods:
- A registry-based observational cohort study included 786 patients with first-ever ischemic stroke.
- Silent lacunes were assessed via brain MRI (none, single, multiple).
- Cox proportional hazard models were used to calculate adjusted hazard ratios (HRs) for outcomes, with follow-up for stroke recurrence or death.
Main Results:
- Multiple silent lacunes were present in 11.1% of patients.
- Increasing numbers of silent lacunes correlated with higher incidence rates of ischemic stroke recurrence.
- Adjusted HR for recurrence was 2.52 (1.25-5.09) for multiple silent lacunes; no significant association found for death or cardiovascular events.
Conclusions:
- In ischemic stroke patients without AF, more silent lacunes are linked to a higher risk of stroke recurrence.
- Multiple silent lacunes significantly increase the risk of recurrent ischemic stroke.
- Silent lacunes did not significantly affect the risk of death or cardiovascular events in this cohort.
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