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Updated: Feb 22, 2026

Motor Dual-Tasks for Gait Analysis and Evaluation in Post-Stroke Patients
Published on: March 11, 2021
The relation between total cerebral small vessel disease burden and gait impairment in patients with minor stroke
Caroline Mj Loos1, Caroline McHutchison2, Vera Cvoro2
11 Department of Neurology and Cardiovascular Research Institute Maastricht (CARIM), Maastricht University Medical Centre (MUMC+), University Maastricht, the Netherlands.
Abstract:
Background and aims Individual MRI markers of cerebral small vessel disease are associated with gait impairment. The impact of total cerebral small vessel disease-related brain damage, expressed by a cerebral small vessel disease MRI burden score, on mobility after stroke, has not been considered, although this score gives a better representation of the overall effect of cerebral small vessel disease on the brain. We determined if the total cerebral small vessel disease burden is associated with gait impairment three years after minor stroke. Methods In total, 200 patients with minor lacunar or non-lacunar stroke (NIHSS ≤ 7) underwent a brain MRI at presentation. Presence of lacunes, white matter hyperintensities, cerebral microbleeds, and perivascular spaces were summed in a total cerebral small vessel disease MRI burden score (range 0-4). Gait disturbances, measured by timed-up-and-go test and self-reported stroke impact scale mobility domain were assessed three years after stroke. We tested associations adjusted for key variables by linear regression analysis. Results Total cerebral small vessel disease burden was not associated with gait impairment after minor stroke in all patients, nor in lacunar stroke patients ( n = 87). In non-lacunar stroke patients ( n = 113), total cerebral small vessel disease burden was associated with lower stroke impact scale mobility domain scores, independent of age, vascular risk factors, and stroke severity (unstandardized B -4.61; 95% CI -8.42; -0.79, p < 0.05). Conclusion Patients with non-lacunar stroke and a higher total cerebral small vessel disease burden have more subjective mobility impairment three years after stroke. The total cerebral small vessel disease MRI burden score is a possible marker to identify patients at risk for subjective gait impairment. These findings should be confirmed in larger studies.
Insights
A higher burden of cerebral small vessel disease (CSVD) on MRI is linked to mobility issues three years after non-lacunar stroke. This CSVD MRI burden score may identify patients at risk for gait impairment.
Area of Science:
- Neurology
- Radiology
- Gerontology
Background:
- Cerebral small vessel disease (CSVD) is a common cause of stroke.
- Individual MRI markers of CSVD are known to affect gait.
- The cumulative effect of CSVD on mobility post-stroke needs further investigation.
Purpose of the Study:
- To determine if the total CSVD MRI burden score is associated with gait impairment three years after minor stroke.
- To investigate the impact of overall CSVD brain damage on post-stroke mobility.
Main Methods:
- 200 patients with minor stroke underwent brain MRI to calculate a CSVD burden score (0-4) based on lacunes, white matter hyperintensities, microbleeds, and perivascular spaces.
- Gait was assessed three years post-stroke using the Timed-Up-and-Go test and the Stroke Impact Scale mobility domain.
- Linear regression analysis was used to test associations, adjusted for key variables.
Main Results:
- Total CSVD burden was not associated with gait impairment in all patients or in lacunar stroke patients.
- In non-lacunar stroke patients, higher total CSVD burden correlated with lower self-reported mobility scores (p < 0.05).
- This association remained significant after adjusting for age, vascular risk factors, and stroke severity.
Conclusions:
- Non-lacunar stroke patients with a higher CSVD MRI burden experience more subjective mobility impairment long-term.
- The CSVD MRI burden score may serve as a valuable tool for identifying individuals at risk of gait disturbances after stroke.
- Further validation in larger cohorts is recommended.

