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Updated: Apr 15, 2026

Evaluation of the Cognitive Performance of Hypertensive Patients with Silent Cerebrovascular Lesions
Published on: April 23, 2021
Lesion load may predict long-term cognitive dysfunction in multiple sclerosis patients
Francesco Patti1, Manuela De Stefano2, Luigi Lavorgna2
1Department G.F. Ingrassia, Section of Neurosciences, University of Catania, Catania, Italy.
Background:
Magnetic Resonance Imaging (MRI) techniques provided evidences into the understanding of cognitive impairment (CIm) in Multiple Sclerosis (MS).
Objectives:
To investigate the role of white matter (WM) and gray matter (GM) in predicting long-term CIm in a cohort of MS patients.
Methods:
303 out of 597 patients participating in a previous multicenter clinical-MRI study were enrolled (49.4% were lost at follow-up). The following MRI parameters, expressed as fraction (f) of intracranial volume, were evaluated: cerebrospinal fluid (CSF-f), WM-f, GM-f and abnormal WM (AWM-f), a measure of lesion load. Nine years later, cognitive status was assessed in 241 patients using the Symbol Digit Modalities Test (SDMT), the Semantically Related Word List Test (SRWL), the Modified Card Sorting Test (MCST), and the Paced Auditory Serial Addition Test (PASAT). In particular, being SRWL a memory test, both immediate recall and delayed recall were evaluated. MCST scoring was calculated based on the number of categories, number of perseverative and non-perseverative errors.
Results:
AWM-f was predictive of an impaired performance 9 years ahead in SDMT (OR 1.49, CI 1.12-1.97 p = 0.006), PASAT (OR 1.43, CI 1.14-1.80 p = 0.002), SRWL-immediate recall (OR 1.72 CI 1.35-2.20 p<0.001), SRWL-delayed recall (OR 1.61 CI 1.28-2.03 p<0.001), MCST-category (OR 1.52, CI 1.2-1.9 p<0.001), MCST-perseverative error(OR 1.51 CI 1.2-1.9 p = 0.001), MCST-non perseverative error (OR 1.26 CI 1.02-1.55 p = 0.032).
Conclusion:
In our large MS cohort, focal WM damage appeared to be the most relevant predictor of the long-term cognitive outcome.
Insights
Focal white matter damage, measured by MRI, significantly predicts long-term cognitive impairment in Multiple Sclerosis (MS) patients. This finding highlights the importance of tracking white matter lesions for understanding cognitive decline in MS.
Area of Science:
- Neuroimaging
- Neurology
- Cognitive Science
Background:
- Magnetic Resonance Imaging (MRI) has provided insights into cognitive impairment (CIm) in Multiple Sclerosis (MS).
- Understanding the predictors of long-term CIm is crucial for managing MS patients.
Purpose of the Study:
- To determine the predictive role of white matter (WM) and gray matter (GM) integrity on long-term cognitive function in a cohort of MS patients.
- To assess the relationship between baseline MRI parameters and cognitive performance over a nine-year period.
Main Methods:
- A cohort of 303 MS patients from a previous MRI study were followed up.
- Baseline MRI parameters including cerebrospinal fluid fraction (CSF-f), WM fraction (WM-f), GM fraction (GM-f), and abnormal WM fraction (AWM-f) were quantified.
- Cognitive status was assessed after nine years using SDMT, SRWL (immediate and delayed recall), MCST (categories, perseverative and non-perseverative errors), and PASAT.
Main Results:
- Abnormal white matter fraction (AWM-f) was a significant predictor of impaired performance in SDMT, PASAT, SRWL (immediate and delayed recall), and MCST (categories, perseverative and non-perseverative errors) nine years later.
- Higher AWM-f at baseline was associated with worse cognitive outcomes across multiple tests.
- The predictive value of AWM-f was statistically significant for all tested cognitive domains.
Conclusions:
- Focal white matter damage, quantified by AWM-f, is the most significant predictor of long-term cognitive outcomes in patients with Multiple Sclerosis.
- MRI-based assessment of white matter lesions is valuable for predicting the trajectory of cognitive impairment in MS.
- These findings underscore the importance of monitoring white matter integrity for managing cognitive health in MS.
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