Neuropsychological features in childhood and juvenile multiple sclerosis Five-year follow-up

被引:102
作者
Amato, Maria P. [1 ]
Goretti, Benedetta [1 ]
Ghezzi, Angelo [2 ]
Hakiki, Bahia [1 ]
Niccolai, Claudia [1 ]
Lori, Silvia [1 ]
Moiola, Lucia [3 ]
Falautano, Monica [3 ]
Viterbo, Rosa G. [4 ]
Patti, Francesco [5 ]
Cilia, Sabina [5 ]
Pozzilli, Carlo [6 ]
Bianchi, Valentina [6 ]
Roscio, Marco [2 ]
Martinelli, Vittorio [3 ]
Comi, Giancarlo [3 ]
Portaccio, Emilio [1 ]
Trojano, Maria [4 ]
机构
[1] Univ Florence, Dept NEUROFARBA, I-50121 Florence, Italy
[2] Hosp Gallarate, MS Ctr, Gallarate, Italy
[3] IRCCS Hosp San Raffaele, Dept Neurol, Milan, Italy
[4] Univ Bari, Dept Neurosci & Sense Organs, I-70121 Bari, Italy
[5] Univ Polyclin Hosp G Rodolico, Multiple Sclerosis Ctr, Catania, Italy
[6] Univ Roma La Sapienza, Dept Neurol Sci, I-00185 Rome, Italy
关键词
COGNITIVE IMPAIRMENT; PSYCHOSOCIAL FEATURES; CHILDREN; ADOLESCENTS; MS; SCALE;
D O I
10.1212/WNL.0000000000000885
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: The aim of the study was to perform a third cognitive assessment in our pediatric-onset multiple sclerosis (MS) patient cohort and determine predictors of the individual cognitive outcome. Methods: After 4.7 +/- 0.7 years from baseline evaluation, 48 of 63 patients in the original cohort were reassessed on an extensive neuropsychological battery and compared with 46 healthy controls. Two alternate versions of the tests were used at different assessment points. Cognitive impairment was defined as the failure of >= 3 tests; individual change in the cognitive impairment index was measured. Results: At year 5, 38% of the subjects with MS fulfilled our criterion for impairment. Between years 2 and 5, regarding individual cognitive impairment index change, 66.7% of the patients improved. However, comparing baseline and 5-year testing (when the same versions of the tests were used), cognitive impairment index deterioration was observed in 56% of the patients, improvement in 25%, and stability in 18.8%. A deteriorating performance was related to male sex, younger age and age at MS onset, and lower education. None of these variables, however, was retained in the multivariate analysis. Conclusions: Cognitive outcome in pediatric-onset MS can be heterogeneous. Progression of cognitive problems in a few subjects and potential for compensation and improvement in others call for systematic cognitive screening in this population and development of effective treatment strategies.
引用
收藏
页码:1432 / 1438
页数:7
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