Cognitive impairment and structural brain changes in patients with clinically isolated syndrome at high risk for multiple sclerosis
Language English Country Germany Media print-electronic
Document type Journal Article
PubMed
28028623
DOI
10.1007/s00415-016-8368-9
PII: 10.1007/s00415-016-8368-9
Knihovny.cz E-resources
- Keywords
- Clinically isolated syndrome, Cognition, MRI, Multiple sclerosis, Neuropsychology, Voxel-based morphometry,
- MeSH
- Atrophy MeSH
- Demyelinating Diseases complications diagnostic imaging psychology MeSH
- Adult MeSH
- Cognitive Dysfunction diagnostic imaging etiology MeSH
- Humans MeSH
- Magnetic Resonance Imaging MeSH
- Brain diagnostic imaging MeSH
- Neuropsychological Tests MeSH
- Image Processing, Computer-Assisted MeSH
- Disability Evaluation MeSH
- Prognosis MeSH
- Disease Progression MeSH
- Risk Factors MeSH
- Organ Size MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
Patients with clinically isolated syndrome (CIS), unlike those with multiple sclerosis (MS), have a selective cognitive impairment which is not consistently related to structural brain changes. Our objective was to characterize a profile of cognitive impairment and its association with structural brain changes in patients with CIS who are at high risk of developing MS. Patients with CIS at high risk for MS on interferon-beta (n = 51) and age-, gender-, and education-matched controls (n = 44) underwent comprehensive neuropsychological testing and MRI brain scan with voxel-based morphometry. The CIS group had lower cognitive performance in verbal and nonverbal memory, information processing speed/attention/working memory, and executive and visuo-spatial functions compared to controls (p ≤ 0.040). Lower cognitive performance was present in 18-37 and 14-26% of patients with CIS at high risk for MS depending on the criteria used. Brain volume was reduced predominantly in fronto-temporal regions and the thalamus in the CIS group (p ≤ 0.019). Cognitive performance was not associated with structural brain changes except for the association between worse visuo-spatial performance and lower white matter volume in the CIS group (β = 0.29; p = 0.042). Our results indicated that patients with CIS at high risk for MS may have a pattern of lower cognitive performance and regional brain atrophy similar to that found in patients with MS. Lower cognitive performance may be present in up to one-third of patients with CIS at high risk for MS, but, unlike patients with MS, variability in their cognitive performance may lead to a lack of consistent associations with structural brain changes.
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