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Natural history of cognitive deficits and their relationship to MRI T2-hyperintensities in NF1.

Authors :
Hyman SL
Gill DS
Shores EA
Steinberg A
Joy P
Gibikote SV
North KN
Source :
Neurology [Neurology] 2003 Apr 08; Vol. 60 (7), pp. 1139-45.
Publication Year :
2003

Abstract

Background: Cognitive impairment is the most common complication of neurofibromatosis type 1 (NF1) in childhood. Current research suggests a strong relationship between cognitive deficits and brain T2-hyperintensities. The majority of these lesions disappear as the child ages. Cross-sectional data suggest that there also are improvements in intellect.<br />Objective: To determine the natural history of cognitive functioning and MRI T2-hyperintensities from childhood into adulthood, and whether changes in MRI T2-hyperintensities over time are predictive of changes in cognitive functioning.<br />Methods: The authors conducted a prospective longitudinal study of a cohort of 32 patients with NF1 and 11 unaffected sibling controls. All patients underwent neuropsychological assessments and 27 children underwent MRI examinations. The patients were then reassessed after an 8-year period.<br />Results: and<br />Conclusions: There was no improvement in cognitive ability as the children with NF1 developed into adulthood compared with controls. Despite significant decreases in the number, size, and intensity of the T2-hyperintensities over the 8-year period, these changes were not associated with changes in cognitive ability. T2-hyperintensities in the cortex or subcortical or deep white matter are more frequent with age and these lesions are likely to have a different pathology than basal ganglia lesions. The best predictor of cognitive dysfunction in adulthood was the presence of T2-hyperintensities in childhood, rather than current lesion status. There is a limited time window (<18 years) in which the presence of T2-hyperintensities can be used as biologic markers of cognitive dysfunction.

Details

Language :
English
ISSN :
1526-632X
Volume :
60
Issue :
7
Database :
MEDLINE
Journal :
Neurology
Publication Type :
Academic Journal
Accession number :
12682321
Full Text :
https://doi.org/10.1212/01.wnl.0000055090.78351.c1