Early imaging predicts later cognitive impairment in primary progressive multiple sclerosis

被引:44
|
作者
Penny, S. [1 ]
Khaleeli, Z. [1 ]
Cipolotti, L. [2 ]
Thompson, A. [1 ]
Ron, M. [1 ]
机构
[1] UCL, Inst Neurol, Dept Neuroinflammat, London WC1N 3BG, England
[2] Natl Hosp Neurol & Neurosurg, Dept Psychol, London WC1N 3BG, England
关键词
MAGNETIZATION-TRANSFER RATIO; WHITE-MATTER; NEUROPSYCHOLOGICAL IMPAIRMENT; BRAIN ATROPHY; DISABILITY; GRAY; DEMYELINATION; MARKER; CORTEX;
D O I
10.1212/WNL.0b013e3181cff6a6
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Cognitive impairment in primary progressive multiple sclerosis (PPMS) is common and correlates modestly with contemporary lesion burden and brain volume. Using a cohort/case control methodology, we explore the ability of MRI abnormalities, including those in the normal-appearing brain tissue, to predict future cognitive dysfunction in PPMS. Methods: Thirty-one patients recruited into a longitudinal study within 5 years of onset of PPMS were assessed neuropsychologically on average 5.5 years later along with 31 matched healthy controls. MRI data obtained at entry into the study (lesion metrics, brain volumes, magnetization transfer ratio histogram metrics, and magnetic resonance spectroscopy metabolite concentrations) were used to predict cognitive impairment at follow-up. Results: Twenty-nine percent of patients were categorized as cognitively impaired. T2 lesion volume was the best MRI predictor of overall cognitive function and performance on tests of verbal memory and attention/speed of information processing. Low gray matter magnetization transfer ratio was the best predictor of poor performance on a further test of attention/speed of information processing and an executive function test. Low gray and white matter volumes were independent predictors of poor performance on a second test of executive function. Conclusions: MRI abnormalities observed in early primary progressive multiple sclerosis can predict cognitive impairment 5 years later. While focal damage disrupting white matter tracts appears to be the most important predictor of subsequent cognitive dysfunction, gray matter pathology also plays a role. Neurology (R) 2010; 74: 545-552
引用
收藏
页码:545 / 552
页数:8
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